September 29, 2003
Baxter Healthcare Anesthesia Has
Recalled Sodium Nitroprusside Injection
The FDA has released the following information.
Sodium Nitroprusside Injection, 50 mg/2mL single dose vial, For Intravenous
Infusion Only, Rx only. Baxter Mfd. for an affiliate of Baxter Healthcare
Corp., Deerfield, IL. Recall # D-319-3.
00K113, exp 08/03; 00N107, exp 10/03; 00S110, exp 12/03; 01B117, exp 02/04;
01H101, exp 06/04; 02A127, exp 01/05; 02C112, exp 03/05; 02E104, exp 05/05;
03C119, exp 03/06.
Recalling Firm: Baxter Healthcare Anesthesia and Critical Care, New
Providence, NJ, by letter on July 31, 2003.
Manufacturer: Gensia Sicor Pharmaceuticals, Inc, Irvine, CA. Firm initiated
recall is ongoing.
VOLUME OF PRODUCT IN COMMERCE