Drug recall D-1025-2022
Product
Amoxicillin Capsules, USP, 500 mg, 100-count bottle, Rx only, MFG: Sandoz Pharma, NDC 0781-2613-01
Reason for recall
cGMP deviations: Temperature abuse
Lots and codes
McKesson Medical-Surgical (MMS) is not able to identify the particular lot number received by a particular consignee for the recalled prescription products. Each letter includes the date it was distributed to customers and the dates that impacted product may have been shipped to the customer.
Recall details
- Recalling firm
- Mckesson Medical-Surgical Inc. Corporate Office, Richmond, VA
- Quantity
- 12 bottles
- Distribution
- USA nationwide.
- Type
- Voluntary: Firm initiated
- Recall initiated
- April 13, 2022
- Terminated
- November 30, 2023
Related products
- Amoxicillin – drug information
- NDC 0781-6156 Amoxicillin · Amoxicillin 200 mg/5mL · Sandoz Inc
- NDC 0781-5061 Amoxicillin · Amoxicillin 875 mg/1 · Sandoz Inc
- NDC 0781-5060 Amoxicillin · Amoxicillin 500 mg/1 · Sandoz Inc
- NDC 0781-6041 Amoxicillin · Amoxicillin 250 mg/5mL · Sandoz Inc
- NDC 0781-6157 Amoxicillin · Amoxicillin 400 mg/5mL · Sandoz Inc
- NDC 0781-6039 Amoxicillin · Amoxicillin 125 mg/5mL · Sandoz Inc
- NDC 0781-2020 Amoxicillin · Amoxicillin 250 mg/1 · Sandoz Inc
- NDC 0781-2613 Amoxicillin · Amoxicillin 500 mg/1 · Sandoz Inc