PlainRecalls
FDA Drug Moderate Class II Terminated

Acyclovir Tablets USP 800 mg ,(NDC 60505-5307-1), Rx only, Manufactured by Apotex Inc., Toronto, Ontario, Canada M9L 1T9, Manufactured for Apotex Corp.,Weston, Florida 33326.

Reported: December 4, 2013 Initiated: July 17, 2013 #D-017-2014

Product Description

Acyclovir Tablets USP 800 mg ,(NDC 60505-5307-1), Rx only, Manufactured by Apotex Inc., Toronto, Ontario, Canada M9L 1T9, Manufactured for Apotex Corp.,Weston, Florida 33326.

Reason for Recall

Presence of Particulate Matter: Product from lot KF2199, may contain tablets with pieces of nitrile rubber glove embedded within the tablets.

Details

Recalling Firm
Apotex Inc.
Units Affected
4,844 bottles
Distribution
Nationwide and Puerto Rico
Location
Toronto, N/A

Frequently Asked Questions

What product was recalled?
Acyclovir Tablets USP 800 mg ,(NDC 60505-5307-1), Rx only, Manufactured by Apotex Inc., Toronto, Ontario, Canada M9L 1T9, Manufactured for Apotex Corp.,Weston, Florida 33326.. Recalled by Apotex Inc.. Units affected: 4,844 bottles.
Why was this product recalled?
Presence of Particulate Matter: Product from lot KF2199, may contain tablets with pieces of nitrile rubber glove embedded within the tablets.
Which agency issued this recall?
This recall was issued by the FDA Drug on December 4, 2013. Severity: Moderate. Recall number: D-017-2014.