SCA Pharmaceuticals, LLC: Drug Recall
Recall #D-0408-2024 · 11/09/2023
Class II: Risk
Recall Details
- Recall Number
- D-0408-2024
- Classification
- Class II
- Product Type
- Drug
- Recalling Firm
- SCA Pharmaceuticals, LLC
- Status
- Terminated
- Date Initiated
- 11/09/2023
- Location
- Windsor, CT, United States
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 399 syringes
Reason for Recall
Lack of Assurance of Sterility
Product Description
HYDROmorphone HCl 25 mg/25 mL in 0.9% Sodium Chloride Injection, (Concentration = 1mg/mL), 25 mL fill 30 mL Syringe, Rx only, SCA Pharmaceuticals, 755 Rainbow Rd., Windsor, CT 06095, NDC 70004-0303-17, Bar Code 7004030317
Distribution Pattern
Nationwide in the USA
Other Recalls by SCA Pharmaceuticals, LLC
- Class II: Risk 11/09/2023
- Class II: Risk 11/09/2023
- Class II: Risk 11/09/2023
- Class II: Risk 11/09/2023
- Class II: Risk 11/09/2023
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.