FDAFDA · Food and drugs·Recall number D-268-2013
Amoxicillin Capsules USP 500 mg, Manufactured in Austria by Sandoz GmbH for Sandoz Inc., Princeton, NJ 08540, Rx only. Manufactured in 500 ct (NDC 0781-2613-05) and 30 ct (NDC 0781-2613-31) bottles.
Published May 1, 2013 · Recall initiated: April 18, 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 Foreign Substance, Sandoz is recalling certain lots of Amoxicillin Capsules, USP 500 mg due to potential contamination with fragments of stainless steel wire mesh.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Brand
- AMOXICILLIN
- Manufacturer
- Sandoz Incorporated
- Distributor
- Nationwide
- UPC
- 0307816156526
- Lot
- CK2003, CK2004 exp. 04/15, CR4110, CR4111, CS2983, CS2986, CS2988, CS2989, CS2990, CS2991, CS2992, CS2993, CS2994 exp. 07/15, CK3616, CK3617 exp. 04/15
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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