FDA Enforcement
Class II
Terminated
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.
Recall: Z-1802-2014
·
Reported June 25, 2014
Enforcement
- Recall Number
- Z-1802-2014
- Event ID
- 68216
- Classification
- Class II
- Status
- Terminated
- Product Type
- Devices
- Firm
- Biomet, Inc.
- Voluntary / Mandated
- Voluntary: Firm initiated
- Initial Notification
- Letter
- Report Date
- June 25, 2014
- Initiation Date
- April 15, 2014
- Classification Date
- June 16, 2014
- Termination Date
- July 7, 2015
- Address
- 56 E Bell Dr, N/A, Warsaw, IN, 46582-6989, United States
Description
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
The nitinol wire or monofilament may buckle within the EZPass Suture Passer and become kinked making the wire/monofilament difficult to use.
Code Info
Part numbers 110007379 Lot 060830 and 258920,
Distribution
Nationwide Distribution.
Quantity
100 units