Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Enoxaparin Sodium Injection Recalled by Cardinal Health Inc. Due to Correct Labeled Product Mispack: Bags labeled for Enoxaparin...
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 Cardinal Health Inc. directly.
Affected Products
Enoxaparin Sodium Injection, USP, 30 mg/0.3 mL, packaged in 0.3 mL prefilled syringes further packaged in bags of 5 prefilled syringes, Rx Only, Dist. by: Sandoz Inc., Princeton, NJ 08540, Outer package - NDC 55154-3543-5, Inner label - NDC 0781-3238-01
Quantity: 10 bags
Why Was This Recalled?
Correct Labeled Product Mispack: Bags labeled for Enoxaparin Sodium Injection, 80 mg/0.8 mL, contained Enoxaparin Sodium Injection, 30 mg/0.3 mL
Where Was This Sold?
This product was distributed to 1 state: KS
About Cardinal Health Inc.
Cardinal Health Inc. has 240 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report