Drug recall D-1179-2017
Product
Ampicillin for Injection, USP, 500 mg per vial, single vial (NDC 0781-3407-78) packaged in 10-count shrink wrap packs (NDC 0781-3407-95), Rx only, Manufactured in Austria by Sandoz GmbH or Sandoz Inc., Princeton, NJ 08540.
Reason for recall
Labeling: Missing Label: customer complaint that some vials of ampicillin within the shrink wrap pack are missing labels.
Lots and codes
Lot: GH8254, Exp 06/19
Recall details
- Recalling firm
- Sandoz Inc, Princeton, NJ
- Quantity
- 13,435 shrink wrap packs
- Distribution
- Nationwide in the USA and Puerto Rico
- Type
- Voluntary: Firm initiated
- Recall initiated
- September 25, 2017
- Terminated
- April 8, 2019
Related products
- Ampicillin – drug information
- NDC 0781-3407 Ampicillin · Ampicillin Sodium 500 mg/1 · Sandoz Inc
- NDC 0781-3402 Ampicillin · Ampicillin Sodium 250 mg/1 · Sandoz Inc
- NDC 0781-3408 Ampicillin · Ampicillin Sodium 2 g/1 · Sandoz Inc
- NDC 0781-3400 Ampicillin · Ampicillin Sodium 125 mg/1 · Sandoz Inc
- NDC 0781-3404 Ampicillin · Ampicillin Sodium 1 g/1 · Sandoz Inc