Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Portex LineDraw Arterial Blood Sampling Syringe with Dry Lithium Heparin Recalled by Smiths Medical ASD, Inc. Due to Portex Pro-Vent and LineDraw Arterial Blood Sampling syringes...
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 Smiths Medical ASD, Inc. directly.
Affected Products
Portex LineDraw Arterial Blood Sampling Syringe with Dry Lithium Heparin for Gases and Electrolytes
Quantity: 720,100 total devices
Why Was This Recalled?
Portex Pro-Vent and LineDraw Arterial Blood Sampling syringes may have broken luers.
Where Was This Sold?
This product was distributed to 34 states: AL, AZ, AR, CA, CO, DE, FL, GA, ID, IL, IN, IA, KS, LA, MD, MA, MI, MN, MS, MO, NE, NJ, NY, NC, OH, OK, OR, PA, RI, SC, TN, TX, UT, VA
About Smiths Medical ASD, Inc.
Smiths Medical ASD, Inc. has 114 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report