PYRIDOXINE HCL 100MG/ML W/PRES recalled over sterility concerns
- Recall date
- May 13, 2016
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Official notice title
- Medaus, Inc. recalls PYRIDOXINE HCL 100MG/ML W/PRES (BENZYL ETOH 0.02%), 5ML Vials, MEDAUS PHARMACY
- Recall number
- D-1236-2016
- FDA classification
- Class III
- Brand / firm
- Medaus, Inc.
- Sold / distributed
- U.S. Nationwide, Japan, and New Zealand.
Why it was recalled
Lack of Assurance of Sterility
Class III means the product violates regulations but is not likely to cause harm.
What was recalled
PYRIDOXINE HCL 100MG/ML W/PRES (BENZYL ETOH 0.02%), 5ML Vials, MEDAUS PHARMACY
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