Inmar Supply Chain Solutions, LLC recalls All Over-The-Counter (OTC) drug products warehoused, salvaged, and sold by Inmar.
CGMP Deviations: Potential exposure to rodents and rodent activity in the distribution center. Also, due to unusually hot weather, FDA Recalled Products may have been subjected to temperatures in excess of storage…
Read the official notice →- Date
- 2023-08-30
- Country
- United States
- Brand
- Inmar Supply Chain Solutions
- Product
- All Over-The-Counter (OTC) drug products warehoused, salvaged, and sold by Inmar.
- Classification
- Class II
- Units
- Separate Distribution List (salvage buyers) provided by Inmar and will be…
- Category
- Drugs & medical
- Source
- FDA · Drug
Copied automatically from the US Food and Drug Administration. Details may be shortened or out of date; the official notice is the authoritative source. Disclaimer
What to do
- Check the product name, strength and lot number against the official notice.
- Do not stop a prescribed medicine without talking to your doctor or pharmacist first.
- Ask the pharmacy or supplier about a replacement or refund.
General guidance from Recall Atlas. The official notice from the US Food and Drug Administration has the exact models, batch codes and remedy, and it takes priority.
More Inmar Supply Chain Solutions recalls
- 2023-10-04
USInmar Supply Chain Solutions, LLC recalls Various Medical Products stored on pallets, including but not limited to bandages, tampons, condoms, blood glucose monitors,…
Various medical devices potentially exposed to rodent and rodent activity. In addition, medical devices may have been subjected to temperatures in excess of storage requirements on product labeling.
- 2023-08-30
- US
Inmar Supply Chain Solutions, LLC recalls Multiple FDA-regulated products. Pallets
Potential exposure to rodents and rodent activity in the warehouse.
Other drugs & medical recalls in the United States
- 2023-08-30
- US
ICU Medical Inc recalls Plum 360 Infusion System, List Numbers: 300100405, 300100409, 300100413, 300100414, 300100415, 300100418, 300100451, 300100452, 300100453,…
Due to a manufacturing defect of a supplier provided component, there is a potential that the audible signal for an alarm may not sound under certain conditions.
- US
Draeger Medical, Inc. recalls Carina Sub-Acute Care Ventilator
Presence of polyether polyurethane (PE-PUR) and emission of 1,3-Dichloropropan-2-ol that exceed the acceptable uptake level during continuous use (>30 days) in pediatric patients.
- US
TMC Acquisitions LLC dba Tailor Made Compounding recalls Semaglutide/Cyanocobalamin 2mg/0.4mg/mL, 1mLvials, Tailor Made Compounding.
Lack of Assurance of Sterility
FDA · DrugTMC Acquisitions LLC dba Tailor Made CompoundingNationwide within the USAOfficial notice → - US
Baxter Healthcare Corporation recalls Bendamustine HCl Injection, 100mg/4mL (25mg/mL), One 4 mL Multiple-Dose Vial, Rx only, Manufactured for Baxter Healthcare…
Labeling: Missing Label; customer complaint received that labels were partially or completely peeled off injection vial.
- US
Ecometics, Inc. recalls activator concentrate, Sodium Fluoride 0.96% in Activator Concentrate; 0.08% in diluted Activator Solution, Net 1 FL. OZ., Manufactured…
CGMP Deviations: Products not manufactured under current good manufacturing practices.
- US
Glenmark Pharmaceuticals Inc., USA recalls Trandolapril and Verapamil Hydrochloride Extended-Release Tablets 2 mg / 180 mg, 100-count Bottle, Rx only, Manufactured by:…
Subpotent: Out of Specification for Assay Test at the 3-month time point.