Reported Oct 11, 2017 · Terminated
Deferoxamine Mesylate for injection, USP, Single-use Vial, 500 mg/vial, 10 mL vial. Intravenous, Intramuscular,…
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 E 42nd St · New York, NY · 10017-5703
Is this the product you have?
- Deferoxamine Mesylate for injection, USP, Single-use Vial, 500 mg/vial, 10 mL vial. Intravenous, Intramuscular, Subcutaneous Use, Rx Only, Hospira, Inc., Lake Forest IL USA, NDC 0406-2336-10.
- Lot codes and dates
- Lot
51275DDExp. 09/01/17
- Lot
- Amount recalled
- 32,276 10 mL vials
Where it was sold
- Nationwide
Why it was recalled
CGMP Deviations: Firm failed to control impurity for color change at the API stage.
This product is unlikely to cause harm, but it breaks a safety or labelling rule.
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