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.
Reported: January 7, 2015 Initiated: November 21, 2014 #Z-0897-2015
Product Description
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.
Reason for Recall
Needle is not captured in the needle safety sheath in specific lots.
Details
- Recalling Firm
- Smiths Medical ASD, Inc.
- Units Affected
- 334,000
- Distribution
- 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
- Location
- Keene, NH
Frequently Asked Questions
What product was recalled? ▼
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.. Recalled by Smiths Medical ASD, Inc.. Units affected: 334,000.
Why was this product recalled? ▼
Needle is not captured in the needle safety sheath in specific lots.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on January 7, 2015. Severity: Moderate. Recall number: Z-0897-2015.
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