Recalls / Class II
Class IID-1229-2016
Product
NA ASCORBATE 500MG/ML NON-CORN (PF), In a) 10ML Vials, b) 50ML Vials, and c) 100ML Vials, MEDAUS PHARMACY
- Affected lot / code info
- a) Lot #: 151201-30, BUD: 05/29/16; Lot #: 151209-26, BUD: 06/06/16; Lot #: 151216-63, BUD: 06/13/16; Lot #: 151231-11, BUD: 06/28/16; Lot #: 160105-4, BUD: 07/03/16; Lot #: 160125-41, BUD: 07/23/16; Lot #: 160211-20, BUD: 08/09/16. b) Lot #: 151201-30, BUD: 05/29/16; Lot #: 151209-26, BUD: 06/06/16; Lot #: 151216-63, BUD: 06/13/16; Lot #: 151231-11, BUD: 06/28/16; Lot #: 160105-4, BUD: 07/03/16; Lot #: 160125-41, BUD: 07/23/16; Lot #: 160511-20, BUD: 08/09/16. c) Lot #: 151201-30, BUD: 05/29/16; Lot #: 151209-26, BUD: 06/06/16; Lot #: 151216-63, BUD: 06/13/16; Lot #: 151231-11, BUD: 06/28/16; Lot #: 160105-4, BUD: 07/03/16; Lot #: 160125-41, BUD: 07/23/16; Lot #: 160511-20, BUD: 08/09/16.
Why it was recalled
Lack of Assurance of Sterility
Recalling firm
- Firm
- Medaus, Inc.
- Notification channel
- Type
- Voluntary: Firm initiated
- Address
- 6801 Cahaba Valley Rd Ste 116, Birmingham, Alabama 35242-9609
Distribution
- Quantity
- 358000 mL in Vials
- Distribution pattern
- U.S. Nationwide, Japan, and New Zealand.
Timeline
- Recall initiated
- 2016-05-13
- FDA classified
- 2016-07-08
- Posted by FDA
- 2016-07-20
- Terminated
- 2017-06-16
- Status
- Terminated
Source: openFDA Drug Enforcement endpoint. Recall record D-1229-2016. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.