Hypodermic Needle Pro¿ Edge" Safety Device recall
Hypodermic Needle Pro¿ Edge" Safety Device 20G x1; Reorder Number: 402010 Product Usage: The Needle Pro¿ Edge Safety Hypodermic Needle is intended…
Why was Hypodermic Needle Pro¿ Edge" Safety Device recalled?
Needle is not captured in the needle safety sheath in specific lots.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Lot Numbers: 2731779, 2763138, 2771516, 2771517
- Product
- Hypodermic Needle Pro¿ Edge" Safety Device 20G x1; Reorder Number: 402010 Product Usage: The Needle Pro¿ Edge Safety Hypodermic Needle is intended…
- Recalling firm
- Smiths Medical ASD, Inc.
- Quantity
- 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
- Recall date
- January 7, 2015
- Classification
- Class II
- Status
- Completed
- Agency
- FDA (device)