FDAFDA · Food and drugs·Recall number D-017-2014
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.
Published December 4, 2013 · Recall initiated: July 17, 2013
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Presence of Particulate Matter: Product from lot KF2199, may contain tablets with pieces of nitrile rubber glove embedded within the tablets.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Brand
- ACYCLOVIR
- Manufacturer
- Apotex Inc.
- Distributor
- Nationwide and Puerto Rico
- Lot
- Lot # KF2199 Exp 07/15
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- Canada