PlainRecalls
FDA Drug Low Class III Terminated

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.

Reported: October 4, 2017 Initiated: September 25, 2017 #D-1179-2017

Product Description

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.

Details

Recalling Firm
Sandoz Inc
Units Affected
13,435 shrink wrap packs
Distribution
Nationwide in the USA and Puerto Rico
Location
Princeton, NJ

Frequently Asked Questions

What product was recalled?
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.. Recalled by Sandoz Inc. Units affected: 13,435 shrink wrap packs.
Why was this product recalled?
Labeling: Missing Label: customer complaint that some vials of ampicillin within the shrink wrap pack are missing labels.
Which agency issued this recall?
This recall was issued by the FDA Drug on October 4, 2017. Severity: Low. Recall number: D-1179-2017.