Class III โ€” Low Risk

Low risk โ€” use of or exposure to this product is not likely to cause adverse health consequences.

SODIUM FERRIC GLUCONATE COMPLEX IN SUCROSE INJECTION Recalled by West-Ward Pharmaceuticals Corp. Due to Subpotent Drug: Product has an an out of...

Date: November 17, 2016
Company: West-Ward Pharmaceuticals Corp.
Status: Terminated
Source: FDA (Drug)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact West-Ward Pharmaceuticals Corp. directly.

Affected Products

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

Quantity: 5,142 Shelf-packs

Why Was This Recalled?

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

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About West-Ward Pharmaceuticals Corp.

West-Ward Pharmaceuticals Corp. has 6 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report