Low risk — use of or exposure to this product is not likely to cause adverse health consequences.
Dexamethasone Sodium Phosphate Injection Recalled by West-Ward Pharmaceuticals Corp. Due to Failed Impurities/Degradation Specifications: high out of specification results...
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
Dexamethasone Sodium Phosphate Injection, USP, 4 mg/mL, 1 mL Vials (NDC 0641-6145-01), packaged in 25 x 1 mL Vials per shelf pack (NDC 0641-6145-25), Rx Only, Manufactured by WEST-WARD, Eatontown, NJ 07724 USA.
Quantity: 16,157 shelf packs
Why Was This Recalled?
Failed Impurities/Degradation Specifications: high out of specification results for Dexamethasone adduct (related compound).
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About West-Ward Pharmaceuticals Corp.
West-Ward Pharmaceuticals Corp. has 6 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report