VistaPharm, Inc.: Drug Recall
Recall #D-0018-2023 · 09/30/2022
Class II: Risk
Recall Details
- Recall Number
- D-0018-2023
- Classification
- Class II
- Product Type
- Drug
- Recalling Firm
- VistaPharm, Inc.
- Status
- Terminated
- Date Initiated
- 09/30/2022
- Location
- Largo, FL, United States
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 1980 cups
Reason for Recall
cGMP Deviations: Out of specification for assay of one of the preservative ingredients.
Product Description
Pyridostigmine Bromide Oral Solution, USP 60 mg/5 mL Delivers 5 mL, packaged in 5mL unit-dose cup, Rx only, Dist. by: VistaPharm, NDC 66689-406-01
Distribution Pattern
USA Nationwide
Other Recalls by VistaPharm, Inc.
- Class II: Risk 01/07/2022
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.