SENNA Syrup recall: Sterility Concern
SENNA Syrup (sennosides) 8.8 mg/ 5 mL unit-dose cups, packaged in 24 cups per carton, Mfg for: AvKARE, TN 38478, NDC 50262-731-24.
Why was SENNA Syrup recalled?
Microbial Contamination of Non-Sterile Product
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Lot #: AM1115S, Exp. Date 01/2023
- Product
- SENNA Syrup (sennosides) 8.8 mg/ 5 mL unit-dose cups, packaged in 24 cups per carton, Mfg for: AvKARE, TN 38478, NDC 50262-731-24.
- Recalling firm
- Lohxa, LLC
- Quantity
- 87,840 unit dose cups
- Distribution
- Product was distributed to one wholesale who further distributed the product nationwide in the USA
- Recall date
- January 26, 2022
- Classification
- Class I
- Status
- Terminated
- Agency
- FDA (drug)