EZPass Nylon Monofilament Single Pack — Class II medical device recall Z-1802-2014
Terminated recall by Biomet, Inc., reported 2014-06-25, distributed nationwide. The nitinol wire or monofilament may buckle within the EZPass Suture Passer and become kinked making the wire/
| Recall number | Z-1802-2014 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Biomet, Inc., Warsaw, IN, United States |
| Recall initiated | 2014-04-15 |
| Classified | 2014-06-16 |
| Reported by FDA | 2014-06-25 |
| Terminated | 2015-07-07 |
| Distributed | Nationwide (US) |
| Quantity | 100 units |
| Lot numbers | 060830, 258920 |
| Model numbers | 110007379 |
Product
EZPass Nylon Monofilament Single Pack, Part number 110007379, 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 for recall
The nitinol wire or monofilament may buckle within the EZPass Suture Passer and become kinked making the wire/monofilament difficult to use.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1802-2014. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.