Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Hypodermic Needle Pro¿ Edge" Safety Device with Syringe 20G x1 Recalled by Smiths Medical ASD, Inc. Due to Needle is not captured in the needle safety...
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
Hypodermic Needle Pro¿ Edge" Safety Device with Syringe 20G x1 10mL Luer lock syringe; Reorder Number: 4102010 Product Usage: The Needle Pro¿ Edge Safety Hypodermic Needle is intended for injection or aspiration of fluids utilizing a luer lock or luer slip syringe.
Quantity: 47,200
Why Was This Recalled?
Needle is not captured in the needle safety sheath in specific lots.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
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