Ampicillin for Injection recall: Labeling Error
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.
Why was Ampicillin for Injection recalled?
Labeling: Missing Label: customer complaint that some vials of ampicillin within the shrink wrap pack are missing labels.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Lot: GH8254, Exp 06/19
- 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.
- Recalling firm
- Sandoz Inc
- Quantity
- 13,435 shrink wrap packs
- Distribution
- Nationwide in the USA and Puerto Rico
- Recall date
- October 4, 2017
- Classification
- Class III
- Status
- Terminated
- Agency
- FDA (drug)