Low risk โ use of or exposure to this product is not likely to cause adverse health consequences.
Nicardipine Hydrochloride Injection 25 mg/10 mL (2.5 mg/mL) Recalled by West-ward Pharmaceutical Corp. Due to Failed Impurity/Degradation Specifications; out of specification value for...
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 Pharmaceutical Corp. directly.
Affected Products
Nicardipine Hydrochloride Injection 25 mg/10 mL (2.5 mg/mL), 10 mL single-use vials, Rx Only, Mfd. by Exela Pharma Sciences, LLC, Lenoir, NC, Dist. by: West-ward Pharmaceutical Corp., Eatontown, NJ --- NDC 0143-9689-10
Quantity: Lot PLNJ1201 -16,880 vials ; Lot PLNJ1202 - 16,960 vials
Why Was This Recalled?
Failed Impurity/Degradation Specifications; out of specification value for impurity Nitrophenylpuridine Derivative (NPP-D)
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About West-ward Pharmaceutical Corp.
West-ward Pharmaceutical Corp. has 17 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report