Ecometics, Inc.: Drug Recall
Recall #D-1101-2023 · 08/09/2023
Class II: Risk
Recall Details
- Recall Number
- D-1101-2023
- Classification
- Class II
- Product Type
- Drug
- Recalling Firm
- Ecometics, Inc.
- Status
- Completed
- Date Initiated
- 08/09/2023
- Location
- Norwalk, CT, United States
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 92,967 vials
Reason for Recall
CGMP Deviations: Products not manufactured under current good manufacturing practices.
Product Description
AstrinGyn (Ferric Subsulfate) Aqueous, 259 mg/g, 8 gm Single Use Vials, Manufactured for CooperSurgical, Trumbull, CT 06611, NDC 59365-6065-0, Ref 6065.
Distribution Pattern
Nationwide in the USA
Other Recalls by Ecometics, Inc.
- Class II: Risk 08/09/2023
- Class II: Risk 08/09/2023
- Class II: Risk 08/09/2023
- Class II: Risk 08/09/2023
- Class II: Risk 08/09/2023
Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.