Serious health hazard — there is a reasonable probability that use of or exposure to this product will cause serious adverse health consequences or death.
Treprostinil Injection Recalled by Par Sterile Products LLC Due to Presence of Particulate Matter.
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 Par Sterile Products LLC directly.
Affected Products
Treprostinil Injection, 20 mg/20 mL (1 mg/mL), For Subcutaneous or Intravenous Infusion Only, 20 mL Multiple-Dose Vial, Rx Only, Distributed by: Par Pharmaceutical, Chestnut Ridge, NY 10977. NDC: 42023-206-01
Quantity: 466 vials
Why Was This Recalled?
Presence of Particulate Matter.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Par Sterile Products LLC
Par Sterile Products LLC has 2 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report