Drug recall D-017-2014
Product
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.
Lots and codes
Lot # KF2199 Exp 07/15
Recall details
- Recalling firm
- Apotex Inc., Toronto, N/A
- Quantity
- 4,844 bottles
- Distribution
- Nationwide and Puerto Rico
- Type
- Voluntary: Firm initiated
- Recall initiated
- July 17, 2013
- Terminated
- August 4, 2014
Related products
- Acyclovir – drug information
- NDC 60505-5306 Acyclovir · Acyclovir 400 mg/1 · Apotex Corp.
- NDC 60505-5307 Acyclovir · Acyclovir 800 mg/1 · Apotex Corp.