FDA Device recall Z-0898-2015
Hypodermic Needle Pro¿ Edge" Safety Device with Syringe 20G x1 10mL Luer lock syringe
- FDA Device
- Class II
- completed
- Published 2015-01-07
On 2015-01-07 the FDA classified a Class II recall of Hypodermic Needle Pro¿ Edge" Safety Device with Syringe 20G x1 10mL Luer lock syringe by Smiths Medical Asd, citing needle is not captured in the needle safety sheath in specific lots.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0898-2015 |
| Classification | Class II |
| Status | completed |
| Initiated | 2014-11-21 |
| Published | 2015-01-07 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Smiths Medical Asd |
| Distribution | US |
Product
Hypodermic Needle Pro¿ Edge" Safety Device with Syringe 20G x1 10mL Luer lock syringe; Reorder Number: 4102010 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
Needle is not captured in the needle safety sheath in specific lots.
Identifiers
| code_info | Lot Numbers: 2756526, 2771498 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: completed.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0898-2015%22
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