FDA Device recall Z-1801-2014
EZPass Suture Retriever, Nitinol, Single Pack, Part number 10007380
- FDA Device
- Class II
- terminated
- Published 2014-06-25
On 2014-06-25 the FDA classified a Class II recall of EZPass Suture Retriever, Nitinol, Single Pack, Part number 10007380 by Biomet, citing the nitinol wire or monofilament may buckle within the EZPass Suture Passer and become kinked making the wire/monofilament difficult to use.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1801-2014 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2014-04-15 |
| Published | 2014-06-25 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Biomet |
| Distribution | US |
Product
EZPass Suture Retriever, Nitinol, Single Pack, Part number 10007380. Orthopedic Manual Surgical Instrument, Sterile, single use arthroscopic instrument utilized in conjunction with a nitinol wire to aid in passing suture through soft tissue.
Reason
The nitinol wire or monofilament may buckle within the EZPass Suture Passer and become kinked making the wire/monofilament difficult to use.
Identifiers
| code_info | Part numbers 110007380 Lot 223570 and 803860 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1801-2014%22
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