FDA Enforcement
Class II
Terminated
CR POR FEM HATCP SIZE E/L SIZE F/L Knee Prosthesis
Recall: Z-1030-2018
·
Reported March 21, 2018
Enforcement
- Recall Number
- Z-1030-2018
- Event ID
- 78706
- Classification
- Class II
- Status
- Terminated
- Product Type
- Devices
- Firm
- Zimmer Biomet, Inc.
- Voluntary / Mandated
- Voluntary: Firm initiated
- Initial Notification
- Letter
- Report Date
- March 21, 2018
- Initiation Date
- November 29, 2017
- Classification Date
- March 14, 2018
- Termination Date
- April 2, 2020
- Address
- 1800 W Center St, Warsaw, IN, 46580-2304, United States
Description
CR POR FEM HATCP SIZE E/L SIZE F/L Knee Prosthesis
Reason
The LDPE bag packaging for various highly polished hip and knee implants may adhere to the highly polished surface, leaving residue or material from the LDPE bag on the implant after it is removed from the bag.
Code Info
Item Number: 65-5972-015-01 Lot Number: 62086845 Item Number: 65-5972-016-01 Lot Numbers: 11007043 62105229
Distribution
Worldwide Distribution: US (nationwide) and countries of: Argentina, Australia, Brazil, Bolivia, Canada, Chile, China, Colombia, Ecuador, El Salvador, India, Japan, Malaysia, Mexico, Netherlands, New Zealand, Nicaragua, Panama, Seoul-Korea, Singapore, Taiwan, Thailand, and UAE.
Quantity
13,227 in total