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Smiths Medical ASD, Inc. recalls Hypodermic Needle Pro¿ Edge" Safety Device 20G x1; Reorder Number: 402010 Product Usage: The Needle Pro¿ Edge Safet
Recalled January 7, 2015 · FDA recall Z-0897-2015 · Smiths Medical ASD
Hazard
Needle is not captured in the needle safety sheath in specific lots. · FDA Class II
Units
334,000
Sold at
US Nationwide Distribution in the states of AZ CA FL GA IL IN LA MA MN MO MS MT NC ND NJ NV NY OH OR PA RI TN TX VA WA WI WV
Description
Needle is not captured in the needle safety sheath in specific lots.
Product
Hypodermic Needle Pro¿ Edge" Safety Device 20G x1; Reorder Number: 402010 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.
Manufacturer(s)
Smiths Medical ASD, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →