Total Resources International First Aid Kits recall: Contamination
Total Resources International First Aid Kits, Item Numbers: 10HBC01087, 10HBC01092A3PK, 10HBC01112, 10HBC01113, 10HBC01329GLRV1, 10OUT02086GLRV2…
Why was Total Resources International First Aid Kits recalled?
ULTRAtab Laboratories recalled Acetaminophen and electrolyte tablets that were later placed into Total Resources Intl kits. Acetaminophen and electrolyte tablets were recalled due to a Fluid Bed Drier exhaust system breach, which presents the possibility of cross-contamination where the potential contaminations are well known API's at well below efficacious dose levels.
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?
Kit Item No./Lot/Expiration/Best if Used by Date: 10HBC01087/20097-03/6/30/2022; 10HBC01092A3PK/20086-10/6/30/2022; 10HBC01112/20100-10/6/30/2022; 10HBC01113/20062-04, 20063-04, 20064-04, 20083-04, 20084-03, 20085-03, 20104-03, 20105-03, 20106-03/6/30/2022; 10HBC01329GLRV1/20072-05, 20073-05, 20079-05, 20080-05, 20083-05, 20085-05, 20086-05/6/30/2022; 10OUT02086GLRV2/20086-04, 20087-04, 20090-04, 20091-04, 20092-04, 20093-04, 20094-04, 20097-04, 20098-04, 20099-04/6/30/2022; 16BLU01495/ 20079-10/6/30/2022; 20HBC01015CCREV3/20071-10/6/30/2022; 20HBC01084GLOWCC/20090-05, 20091-05, 20092-05, 20093-05/1/31/2022; 20HBC01084GLOWCC/20083-10, 20094-05, 20098-05/5/31/2022; 20HBC01084GLOWCC/20076-01, 20077-01, 20087-05/06/30/2022
- Product
- Total Resources International First Aid Kits, Item Numbers: 10HBC01087, 10HBC01092A3PK, 10HBC01112, 10HBC01113, 10HBC01329GLRV1, 10OUT02086GLRV2…
- Recalling firm
- Total Resources Intl
- Quantity
- 188915
- Distribution
- US: IL, PA, VA, AR, TX, IA, DE, GA, NY, LA, AL, IN, MI, MO, NC, KS, CO, AZ, OH, MS, CA, FL, WI, KY, UT, OR, NH, TN, NV, CT
- Recall date
- May 25, 2022
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)