FDA recall record

Acyclovir Tablets USP 800 mg ,(NDC 60505-5307-1) recall — FDA D-017-2014

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

Class IIclassification
D-017-2014official record ID
Dec 4, 2013report date

Recall record at a glance

Official recordD-017-2014
CategoryDrug Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmApotex Inc.
Report dateDec 4, 2013
Recall initiation dateJul 17, 2013
Quantity4,844 bottles
LocationToronto, N/A, Canada

Official 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.

Why the product was recalled

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

Distribution information

Nationwide and Puerto Rico

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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