Reported Jan 22, 2014 · Terminated
Zithromax (azithromycin for injection), 500 mg/vial, Sterile, Rx Only, For I.V. infusion only, No latex, No…
Pfizer Inc.
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Pfizer Inc. · 235 East 42nd Street · New York, NY · 10017-5703
Is this the product you have?
- Zithromax (azithromycin for injection), 500 mg/vial, Sterile, Rx Only, For I.V. infusion only, No latex, No preservative, Made in Ireland, Distributed by Pfizer Labs, Division of Pfizer Inc, NY, NY 10017, NDC 0069-3150-84
- Lot codes and dates
Lot Number/Expiration Date G81845Exp 10/03/14 0B0CJExp 02/06/15 G44710Exp 07/10/15 G65241Exp 07/11/15 G80003Exp 10/17/15 G82722Exp 11/27/15 G93028G95309
- Exp
01/23/16 G97641Exp 01/30/16
- Amount recalled
- 101,681 Vials
Where it was sold
- Nationwide
- PR
Why it was recalled
Failed Impurities/Degradation Specifications: Pfizer is recalling certain lots due to out of specification results for azithromycin N-oxide degradant.
This product is unlikely to cause harm, but it breaks a safety or labelling rule.
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