Recalled or Not? · Briefings

Daily briefing · 2026-10-13

2026-10-12 13:00 to 2026-10-13 13:00 (UTC; end excluded)

European Union · United States

40 official notices recorded or updated in this observation window, selected for owner review. This is not complete global recall coverage. Some candidates have selection or display-field limits; review the sources.

RASFF · 878318 Aflatoxins in raw peanuts from the United States Risk: serious · information notification for attention Review the official RASFF Window notice. RASFF public summaries do not list brand or operator names — check national food-safety authority advice for consumer product details. Ref 2026.9028 — Notified by Netherlands (NL) — nuts, nut products and seeds

RASFF · 878526 Unauthorised novel food Prekese (Aidan Fruit) from Ghana, via Belgium Risk: potential risk · information notification for follow-up Review the official RASFF Window notice. RASFF public summaries do not list brand or operator names — check national food-safety authority advice for consumer product details. Ref 2026.9027 — Notified by Germany (DE) — herbs and spices

RASFF · 878653 To high intake of curcumin and piperine in food supplements from Austria Risk: potentially serious · information notification for attention Review the official RASFF Window notice. RASFF public summaries do not list brand or operator names — check national food-safety authority advice for consumer product details. Ref 2026.9015 — Notified by Switzerland (CH) — dietetic foods, food supplements and fortified foods

RASFF · 878933 Prohibited tolfenpyrad and exceed maximum levels of pesticides residues: lambda-cyhalothrin 0,091 ± 0,046 mg/kg, thiamethoxam 0,18 ± 0,09 mg/kg; Risk: serious · border rejection notification Review the official RASFF Window notice. RASFF public summaries do not list brand or operator names — check national food-safety authority advice for consumer product details. Ref 2026.9014 — Notified by Latvia (LV) — cocoa and cocoa preparations, coffee and tea

RASFF · 879001 Chlorpyrifos-methyl in fresh peppers from Türkiye Risk: serious · border rejection notification Review the official RASFF Window notice. RASFF public summaries do not list brand or operator names — check national food-safety authority advice for consumer product details. Ref 2026.9016 — Notified by Bulgaria (BG) — fruits and vegetables

RASFF · 879006 Pesticides residues in passion fruit from Ecuador Risk: serious · alert notification Review the official RASFF Window notice. RASFF public summaries do not list brand or operator names — check national food-safety authority advice for consumer product details. Ref 2026.9031 — Notified by Belgium (BE) — fruits and vegetables

RASFF · 879047 Salmonella Enteritidis in frozen chicken gyros from Greece Risk: serious · alert notification Review the official RASFF Window notice. RASFF public summaries do not list brand or operator names — check national food-safety authority advice for consumer product details. Ref 2026.9013 — Notified by Finland (FI) — poultry meat and poultry meat products

RASFF · 879049 aflatoxins in pistacchio paste Risk: potentially serious · alert notification Review the official RASFF Window notice. RASFF public summaries do not list brand or operator names — check national food-safety authority advice for consumer product details. Ref 2026.9030 — Notified by Italy (IT) — nuts, nut products and seeds

RASFF · 879050 Withdrawal of the food supplement “Osavi Hormonal Support Woman - 30 / 60 / 90 vegan caps” marketed to Danish consumers Risk: potential risk · information notification for follow-up Review the official RASFF Window notice. RASFF public summaries do not list brand or operator names — check national food-safety authority advice for consumer product details. Ref 2026.9026 — Notified by Denmark (DK) — dietetic foods, food supplements and fortified foods

RASFF · 879053 formetanate in fresh peppers from Türkiye Risk: serious · border rejection notification Review the official RASFF Window notice. RASFF public summaries do not list brand or operator names — check national food-safety authority advice for consumer product details. Ref 2026.9018 — Notified by Bulgaria (BG) — fruits and vegetables

RASFF · 879057 Acetamiprid аnd Malathion in fresh peppers from Türkiye Risk: serious · border rejection notification Review the official RASFF Window notice. RASFF public summaries do not list brand or operator names — check national food-safety authority advice for consumer product details. Ref 2026.9021 — Notified by Bulgaria (BG) — fruits and vegetables

RASFF · 879109 Absence of official controls and CHED-D for dried ginger from India Risk: no risk · border rejection notification Review the official RASFF Window notice. RASFF public summaries do not list brand or operator names — check national food-safety authority advice for consumer product details. Ref 2026.9024 — Notified by Croatia (HR) — herbs and spices

RASFF · 879114 Aflatoxine B1 in Groundnut from Nicaragua Risk: serious · information notification for attention Review the official RASFF Window notice. RASFF public summaries do not list brand or operator names — check national food-safety authority advice for consumer product details. Ref 2026.9044 — Notified by Netherlands (NL) — nuts, nut products and seeds

RASFF · 879145 Diethyltoluamide in bio kepl origin Canada froM Netherlands Risk: no risk · information notification for follow-up Review the official RASFF Window notice. RASFF public summaries do not list brand or operator names — check national food-safety authority advice for consumer product details. Ref 2026.9036 — Notified by Bulgaria (BG) — dietetic foods, food supplements and fortified foods

RASFF · 879160 Unauthorized treatment with ionizing radiation of frozen Pangasius fillets from Vietnam. Risk: potential risk · border rejection notification Review the official RASFF Window notice. RASFF public summaries do not list brand or operator names — check national food-safety authority advice for consumer product details. Ref 2026.9046 — Notified by Netherlands (NL) — fish and fish products

FDA · D-0688-2026 CAREone, Carbamide Peroxide 6.5%, 0.5 FL OZ (15 mL), Bottle, NDC 72476-838-34 SubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6 7%). The recall is ongoing. Follow the firm and FDA instructions. Lot:1505141, exp 2027-04. Bell Pharmaceuticals, Inc — U.S Nationwide

FDA · D-0712-2026 Amlodipine and Olmesartan Medoxomil Tablets, 10 mg/20 mg, 30 Tablets per bottle, Rx Only, Manufactured by: Alkem Laboratories Ltd., INDIA Failed Dissolution Specifications; Olmesartan Medoxomil content below specifications The recall is ongoing. Follow the firm and FDA instructions. Lot 25121311, expiry 3/31/2028 Ascend Laboratories, LLC — Nationwide in the USA

FDA · D-0728-2026 Xylocaine (lidocaine HCl Injection, USP), 1%, 200 mg per 20 mL (10 mg per mL), 25 Multiple-Dose Vials, 20 mL, Rx only, Sterile, Fresenius Kabi, Lake… Presence of Particulate Matter: Hair was found in products The recall is ongoing. Follow the firm and FDA instructions. Lot #: 6130235, Exp. Date 02/2027 Fresenius Kabi USA, LLC — Nationwide within in the USA

FDA · D-0729-2026 Xylocaine (lidocaine HCl Injection, USP), 1%, 500 mg per 50 mL (10 mg per mL), 25 Multiple-Dose Vials, 50 mL, Rx only, Sterile, Fresenius Kabi, Lake… Presence of Particulate Matter: Hair was found in products The recall is ongoing. Follow the firm and FDA instructions. Lot #: 6133986, Exp. Date 02/2029 Fresenius Kabi USA, LLC — Nationwide within in the USA

FDA · D-0660-2026 Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate and Amphetamine Sulfate Extended-Release Capsules, 5 mg, Rx… Labeling: Label Mix-up: Capsules contain only immediate-release (IR) pellets while labeled as ER capsules. The recall is ongoing. Follow the firm and FDA instructions. Lot#: 25285401A, Exp. Date: 04/2027 Lannett Company Inc. — US Nationwide.

FDA · D-0669-2025 Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate and Amphetamine Sulfate, Extended-Release Capsules, (Mixed… Failed Impurities/Degradation Specifications: The recall is ongoing. Follow the firm and FDA instructions. Lot#: GPC250158A, Exp Date: 06-22-2027 Granules Pharmaceuticals Inc. — Distributed Nationwide in the USA

FDA · D-0670-2025 Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate and Amphetamine Sulfate, Extended-Release Capsules, (Mixed… Failed Impurities/Degradation Specifications: The recall is ongoing. Follow the firm and FDA instructions. lot#: GPC250159A, Exp Date: 06-22-2027 Granules Pharmaceuticals Inc. — Distributed Nationwide in the USA

FDA · D-0671-2025 Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate and Amphetamine Sulfate, Extended-Release Capsules, (Mixed… Failed Impurities/Degradation Specifications: The recall is ongoing. Follow the firm and FDA instructions. Lot#: GPC250178A, Exp Date: 06-22-2027 Granules Pharmaceuticals Inc. — Distributed Nationwide in the USA

FDA · D-0672-2025 Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate and Amphetamine Sulfate, Extended-Release Capsules, (Mixed… Failed Impurities/Degradation Specifications: The recall is ongoing. Follow the firm and FDA instructions. Lot#: GPC250179A, Exp Date: 06-22-2027 Granules Pharmaceuticals Inc. — Distributed Nationwide in the USA

FDA · D-0673-2025 Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate and Amphetamine Sulfate, Extended-Release Capsules, (Mixed… Failed Impurities/Degradation Specifications: The recall is ongoing. Follow the firm and FDA instructions. Lot#: GPC250181A, Exp Date: 06-19-2027 Granules Pharmaceuticals Inc. — Distributed Nationwide in the USA

FDA · D-0608-2024 DELFLEX PERITONEAL DIALYSIS SOLUTION With LOW MAGNESIUM / LOW CALCIUM 4.25% DEXTROSE and attached stay "safe Exchange Set, 2500mL (Approx. 50 mL… This product is being recalled due to the tube weld failure presents itself as a slow leak and can be difficult to detect. The recall is ongoing. Follow the firm and FDA instructions. 24AU03024, exp. date 07/31/2025 Fresenius Medical Care Holdings, Inc. — Nationwide

FDA · D-0615-2025 Sulfamethoxazole and Trimethoprim Tablets, USP 800mg/160mg, Double Strength, Rx Only Presence of a foreign substance.A specific lot of auxiliary polyester coil, used in product packaging was detected with presence of a micro-organism. No micro-organism was detected on any tablets. The recall is ongoing. Follow the firm and FDA instructions. Lot a) AM240173, Exp Date 01/31/2027, AM240680, Exp Date 05/31/2027, AM 240921, Exp Date 06/30/2027, AM241191, Exp Date 08/31/2027. Lot b) AM240176, AM240177, Exp Date 01/31/2027, AM240301, AM240300, Exp Date 02/28/2027, AM240676, AM240677, Exp Date 04/30/2027, AM240678, AM240679, Exp Date 05/30/2027. AM240922, AM240923, AM240924, AM240925, Exp Date 6/30/27, AM241086, Exp Date 7/31/27, AM241087, AM241088, Exp Date 8/31/27. Amneal Pharmaceuticals, LLC — Distributed Nationwide in the USA

FDA · D-0576-2025 Amlodipine and Olmesartan Medoxomil Tablets, 5 mg/ 40 mg, 30-count bottle, Rx Only, Manufactured by: Alkem Laboratories Ltd., INDIA Failed Dissolution Specifications: low dissolution results The recall is ongoing. Follow the firm and FDA instructions. Lot 23121560, Exp 4/30/2026 Ascend Laboratories, LLC — Nationwide in the USA

FDA · D-0587-2024 Dianeal Low Calcium (2.5 mEq/L) Peritoneal Dialysis Solution with 2.5% Dextrose, For Intraperitoneal Administration Only, 6000 mL per bag, Rx Only… Lack of Assurance of Sterility: Potential presence of leaks originating from the Connector Assembly component. The recall is ongoing. Follow the firm and FDA instructions. Lot R24B25FA; Exp. 2/28/2026 Baxter Healthcare Corporation — US Nationwide, Canada

FDA · D-0590-2024 buPROPion Hydrochloride Extended-release Tablets USP (XL) Once-Daily, 150 mg, 100 Tablets (10 x 10) per carton, Rx Only Failed Dissolution Specifications; the product is dissolving faster than the specified limits. The recall is ongoing. Follow the firm and FDA instructions. Lot 1017343, Exp. 12/31/2025 Amerisource Health Services LLC — Nationwide in the USA

FDA · D-0604-2024 Potassium Chloride Extended-Release Capsules, USP, (750 mg) 10 mEq K, 100-count bottle, Rx Only, Manufactured by: Glenmark Pharmaceuticals Ltd. Plot… Failed Dissolution Specifications The recall is ongoing. Follow the firm and FDA instructions. Lot#: 17221446, 17221445, Exp May-31-24; 17221393, 17221403, 17221405, 17221503, 17221508, Exp Jun-30-24; 17221567, 17221566, 17221719, 17221731, Exp Jul-31-24; 17221891, 17221892, 17221900, 17221992, 17222022, Exp Aug-31-24; 17222056, 17222043, 17222068, 17222079, 17222099, 17222103, 17222114, 17222119, 17222188, 17222199, 17222209, 17222200, Exp Sep-30-24; 17222265, 17222269, Exp Oct-31-24; 17222527, 17222530, 17222583, 17222586, 17230051, 17230075, 17230067, Exp Nov-30-24; Glenmark Pharmaceuticals Inc., USA — Nationwide

FDA · D-0605-2024 Potassium Chloride Extended-Release Capsules, USP, (750 mg) 10 mEq K, 500-count bottle, Rx Only, Manufactured by: Glenmark Pharmaceuticals Ltd. Plot… Failed Dissolution Specifications The recall is ongoing. Follow the firm and FDA instructions. Lot #: 17221197, 17221386, 17221385, Exp May-31-24; 17221489, 17221504, 17221530, Exp Jun-30-24; 17221561, 17221579, 17221568, 17221702, 17221704, Exp Jul-31-24; 17221898, 17221993, 17222029, Exp Aug-31-24; 17222300, 17222304, 17222278, 17222609, 17222395, Exp Oct-31-24; 17222589, 17222605, 17222613, Exp Nov-30-24; Glenmark Pharmaceuticals Inc., USA — Nationwide

FDA · D-0606-2024 Potassium Chloride Extended-Release Capsules, USP, (750 mg) 10 mEq K, 100-count bottle, Rx Only, Manufactured by: Glenmark Pharmaceuticals Ltd. Plot… CGMP Deviations The recall is ongoing. Follow the firm and FDA instructions. Lot #: 17230074, 17230221, Exp Dec-31-24; 17230468, 17230479, 17230553, 17230543, 17230561, Exp Jan-31-25; 17230619, 17230624, Exp Feb-28-25; 17230879, 17230890, 17230918, 17230984, 17230996, 17231002, 17231081, Exp Mar-31-25; 17231102, 17231135, 17231329, Exp Apr-30-25; 17231369, 17231513, Exp May-31-24; 17231516, 17231713, Exp Jun-30-25; 17231909, 17231903, Exp Jul-31-25; 17231943, Exp Aug-31-25; 17232166, 17232179, Exp Sep-30-25. Glenmark Pharmaceuticals Inc., USA — Nationwide

FDA · D-0607-2024 Potassium Chloride Extended-Release Capsules, USP, (750 mg) 10 mEq K, 500-count bottle, Rx Only, Manufactured by: Glenmark Pharmaceuticals Ltd. Plot… CGMP Deviations The recall is ongoing. Follow the firm and FDA instructions. Lot #: 17230186, 17230192, 17230213, 17230278, 17230399, Exp Dec-31-24; 17230406, 17230412, 17230427, 17230444, 17230453, 17230495, Exp Jan-31-25; 17230574, 17230585, 17230608, 17230629, Exp Feb-28-25; 17230883, 17230921, Exp Mar-31-25; 17231087, 17231339, Exp Apr-30-25; 17231360, Exp May-31-25; 17231711, 17231745, Exp Jun-30-25; 17231819, 17231820, 17231936, 17231957, Exp Jul-31-25; 17231998, 17232012, Aug-31-25; 17232110, Exp Sep-30-25; 17232114, Exp Aug-31-25; 17232119, 17232343, Exp Sep-30-25. Glenmark Pharmaceuticals Inc., USA — Nationwide

FDA · D-0556-2026 Amlodipine and Olmesartan Medoxomil Tablets, 5mg/40mg, Rx Only, 30-count bottle, Manufactured by: Alkem Laboratories Ltd., India Failed Dissolution Specifications: Olmesartan Medoxomil content below specifications The recall is ongoing. Follow the firm and FDA instructions. Lot: 24123460, Expires: October 31, 2027. Ascend Laboratories, LLC — U.S.A. Nationwide

FDA · D-0532-2025 Lisinopril and Hydrochlorothiazide Tablets USP 20mg/12.5mg, 100-count bottles, Rx only, Mfg for: Lupin Pharmaceuticals, Inc. Baltimore, MD 21202… Product Mix Up: This product is being recalled because of a complaint received that a sealed bottle of lisinopril and hydrochlorothiazide tablets 20mg/12.5 mg had a foreign tablet identified as atazanavir and ritonavir tablet 300mg/100mg. The recall is ongoing. Follow the firm and FDA instructions. Lot #: QA01081, Exp. Date April 2027 Lupin Pharmaceuticals Inc. — Product was distributed nationwide within the United States.

FDA · D-0488-2025 Sulfamethoxazole and Trimethoprim Tablets, USP, 400 mg/80 mg, Rx Only, a) 100 Tablets per Bottle, NDC: 65162-271-10, b) 500 Tablets per Bottle, NDC… Microbial contamination of non-sterile products: tablets may exhibit black spots due to microbial contamination. The recall is ongoing. Follow the firm and FDA instructions. Lot #s: a) AM241019, AM241020, Exp. 06/30/2027 b) AM241019A, Exp 06/30/2027 Amneal Pharmaceuticals, LLC — Nationwide in the USA

CPSC · 27016 DR Power Equipment Recalls Pilot and Premier Trimmer Mowers Due to Risk of Serious Injury or Death from Fire and Burn Hazards Grass and debris can accumulate in the trimmer mowers and ignite, posing a risk of serious injury or death from fire and burn hazards. Consumers should stop using the recalled trimmer mowers immediately and contact DR Power Equipment for a free repair kit. If consumers have concerns about installing the repair kit, contact DR Power Equipment to schedule a free repair installation from an authorized dealer. This recall involves DR Power Equipment Pilot and Premier walk-behind trimmer mowers. The trimmer mowers are orange and black and have the DR Power logo on the top of the motor and on the top of the frame above the cutter head. The trimmer mowers are labeled "Premier" or "Pro" on the side of the frame. The model numbers are printed on a label located on the side of the product's frame. Recalled model numbers and product description, which include

CPSC · 27017 Decathlon America Recalls Van Rysel GRVL AF Bicycles Due to Risk of Serious Injury or Death from Crash Hazard The recalled bicycles’ front lock nut can loosen during use, causing the front wheel to dislodge or loosen over time, posing a crash hazard. Consumers should stop using the recalled bicycles immediately and take them to the nearest Recreational Equipment (REI Co-op) location for a free inspection and repair service of the front fork assembly. Anyone unable to visit an REI Co-op location can contact Decathlon Customer Service directly for assistance. Recalled models can be identified by the Van Rysel Product ID on the top right of the product label under the frame, beginning with the number 5. This recall involves adult multi-terrain gravel bicycles Van Rysel GRVL AF Sword Brown CN FR (model number 8911304), Van Rysel GRVL AF Apex Beige CN FR (model number 8911305), Van Rysel GRVL AF Sword Pink CN FR (model number 8911308), and Van Rysel GRVL AF GRX Black (model num

FDA · Z-0008-2027 Brand Name: Expressaire Product Name: DISPOSABLE TOURNIQUET CUFF, 18" X 4" 1-LINE (CS 10) RED Model/Catalog Number: 564006 Software Version: Not… Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5 years. The recall is ongoing. Follow the firm and FDA instructions. Lot Code: Model Number: 564006 UDI-DI: (01) 00885914044568 All Lots produced from 01SEP2016 to 01MAR2023: S0922STY, S1101STY, S1214STY, R0310STY, R0601STY, R0801STY, R1101STY, R1201STY, Q0930STY, Q1115STY, P1015STY, O0120STY, N0330STY, N0730STY, M0130STY, M0430STY, M0730STY, M0930STY, M1230STY ASP Global, LLC. — US Nationwide distribution in the states of MO, NV, IN, MN, GA, WI, PA, TX, CT, LA, NJ, FL, AL, NY, SC, NE, NC, OH, AZ, CO, MA, IL, KY, CA, VA, ME, KS, MD, TN, MS, AR, WA, NM, MI, WY.

Official sources

Follow the official notice for current instructions.