US Drug Recall Register
Class III · Low risk Terminated Initiated Nov 17, 2016 (10 years ago)

SODIUM FERRIC GLUCONATE COMPLEX IN SUCROSE INJECTION, 62.5mg elemental iron/5mL, 10 (5mL…

Class III — Low risk. Unlikely to cause harm, but violates FDA regulations.

Why it was recalled

Subpotent Drug: Product has an an out of specification in iron assay analysis found during 18 month stability testing.

What was recalled

SODIUM FERRIC GLUCONATE COMPLEX IN SUCROSE INJECTION, 62.5mg elemental iron/5mL, 10 (5mL vials) per shelf pack, Rx only, Mfd: Hikma Farmaceutica (Portugal,) SA Distributed by: Westward Eatowntown NJ 07724 USA, Shelf pack NDC 0143-9570-10, Unit dose NDC 0143-9570-01

Recalling firm
West-Ward Pharmaceuticals Corp.
NDC code
0143-9570-10
Origin
NJ, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0172-2017

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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