FDAClass IIIJune 14, 2017

Acyclovir Tablets recall

Acyclovir Tablets, USP, 800 mg, 100-count bottle, Rx Only, Manufactured for: Camber Pharmaceuticals, Inc., Piscataway, NJ 08854, by Hetero Labs…

Why was Acyclovir Tablets recalled?

Presence of Foreign Substance: human hair melded into tablet.

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 # ACY16075 Exp. 09/2018

Product
Acyclovir Tablets, USP, 800 mg, 100-count bottle, Rx Only, Manufactured for: Camber Pharmaceuticals, Inc., Piscataway, NJ 08854, by Hetero Labs…
Recalling firm
Hetero USA Inc
Quantity
13,692 bottles
Distribution
Nationwide
Recall date
June 14, 2017
Classification
Class III
Status
Terminated
Agency
FDA (drug)
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