Reported Jan 7, 2015 · Completed
Hypodermic Needle Pro¿ Edge" Safety Device 20G x1; Reorder Number: 402010 Product Usage: The Needle Pro¿ Edge Safety…
Smiths Medical ASD, Inc.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Smiths Medical ASD, Inc. · 10 Bowman Dr · Keene, NH · 03431-5043
Is this the product you have?
- Hypodermic Needle Pro¿ Edge" Safety Device 20G x1
- Reorder Number402010
- Product UsageThe Needle Pro¿ Edge Safety Hypodermic Needle is intended for injection or aspiration of fluids utilizing a luer lock or luer slip syringe
- Lot codes and dates
- Lot Numbers
2731779276313827715162771517
- Lot Numbers
- Amount recalled
- 334,000
This recall covers 3 products
The agency filed one notice per product. You are reading one of them; the other 2 are below.
Where it was sold
Why it was recalled
Needle is not captured in the needle safety sheath in specific lots.
This product could cause temporary or reversible health problems — stop using it.
Want the full recall guide?
The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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