Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Potassium Chloride for Inj. Concentrate Recalled by Hospira Inc. Due to Presence of Particulate; red and black particulate within...
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 Hospira Inc. directly.
Affected Products
Potassium Chloride for Inj. Concentrate, USP, 40 mEq (2 mEq/mL), 20 mL Single-dose Fliptop Vial, For IV use, Rx only, Hospira, Inc., Lake Forest, IL 60045 USA
Quantity: 255,900 vials
Why Was This Recalled?
Presence of Particulate; red and black particulate within the solution and embedded within the plastic vial identified as iron oxide
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Hospira Inc.
Hospira Inc. has 245 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report