Reported Aug 26, 2015 · Terminated

AMPICILLIN CAPSULES, USP, 250 mg, 500 count bottles, Rx only, Manufactured for: DAVA Pharmaceuticals, Inc., Fort Lee,…

Vintage Pharmaceuticals LLC, dba Qualitest Pharmaceuticals

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Vintage Pharmaceuticals LLC, DBA Qualitest Pharmaceuticals · 150 Vintage Dr NE · Huntsville, AL · 35811-8216

Is this the product you have?

  • AMPICILLIN CAPSULES, USP, 250 mg, 500 count bottles, Rx only
  • Manufactured forDAVA Pharmaceuticals, Inc., Fort Lee, NJ
  • BySuir Pharma Ireland Ltd., Clonmel, Ireland
  • NDC67253-180-50
Lot codes and dates
  • Lot #: 52217
  • Expiry04/18
Amount recalled
360 Bottles

Where it was sold

Why it was recalled

Labeling: Incorrect Or Missing Package Insert: Product is labeled with unapproved labeling.

This product is unlikely to cause harm, but it breaks a safety or labelling rule.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA drug enforcement) notice

Notice updated Aug 21, 2015 · Data as of Sep 19, 7:18 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.