Status
Terminated
Drug Enforcement D-0421-2024
Lack of Assurance of Sterility
Classification
Class II
Report Date
April 3, 2024
Termination Date
August 27, 2024
Product Information
- Product description
- PHENYLephrine HCl 800 mcg/10 mL in 0.9% Sodium Chloride Injection, (Concentration = 80mcg/mL) 10 mL fill 12 mL Syringe, Rx Only, SCA Pharmaceuticals, 755 Rainbow Rd., Windsor, CT 06095, NDC 70004-0816-12-K, Bar Code 700040081612. (same finished product as F078140, but with RFID for KitCheck compatibility)
- Product quantity
- 2,427 syringes
- Reason for recall
- Lack of Assurance of Sterility
- Recall initiation reason
- —
- Initial firm notification
- Letter
- Distribution pattern
- Nationwide in the USA
Location & Firm
- Recalling firm
- SCA Pharmaceuticals, LLC
- Address
-
755 Rainbow Rd Ste B, N/A
United States - Voluntary / Mandated
- Voluntary: Firm initiated
- Status date
- —
Codes & Dates
- Recall number
- D-0421-2024
- Event ID
- 93456
- Recall initiation date
- November 9, 2023
- Center classification date
- March 22, 2024
- Code info
- Lot #: 1223048610 Exp 04/10/24; 1223048611 Exp 04/10/24; 1223048726 Exp 04/13/24; 1223050163 Exp 06/12/24
- More code info
- —