FDAFDA · Food and drugs·Recall number D-1179-2017
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.
Published October 4, 2017 · Recall initiated: September 25, 2017
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Labeling: Missing Label: customer complaint that some vials of ampicillin within the shrink wrap pack are missing labels.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Brand
- AMPICILLIN
- Manufacturer
- Sandoz Inc
- Distributor
- Nationwide in the USA and Puerto Rico
- Lot
- Lot: GH8254, Exp 06/19
- Risk classification
- Class III
- Area (FDA)
- drug
- Country
- United States
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