FDAClass IIIAugust 26, 2015

Ampicillin Capsules recall: Labeling Error

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

Why was Ampicillin Capsules recalled?

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

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 #: 52217, Expiry: 04/18

Product
AMPICILLIN CAPSULES, USP, 250 mg, 500 count bottles, Rx only, Manufactured for: DAVA Pharmaceuticals, Inc., Fort Lee, NJ, By: Suir Pharma Ireland…
Recalling firm
Vintage Pharmaceuticals LLC, DBA Qualitest Pharmaceuticals
Quantity
360 Bottles
Distribution
U.S. Including: OH
Recall date
August 26, 2015
Classification
Class III
Status
Terminated
Agency
FDA (drug)
Open FDA enforcement record Latest recalls