Hypodermic Needle Pro¿ Edge" Safety Device with Syringe recall
Hypodermic Needle Pro¿ Edge" Safety Device with Syringe 20G x1 5mL Luer lock syringe; Reorder Number: 452010 Product Usage: The Needle Pro¿ Edge …
Why was Hypodermic Needle Pro¿ Edge" Safety Device with Syringe 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 Number: 2755713
- Product
- Hypodermic Needle Pro¿ Edge" Safety Device with Syringe 20G x1 5mL Luer lock syringe; Reorder Number: 452010 Product Usage: The Needle Pro¿ Edge …
- Recalling firm
- Smiths Medical ASD, Inc.
- Quantity
- 10,000
- 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)