FDA Medical Device Recalls (openFDA)
Biomet, Inc.: Various trauma and sports medicine instruments and implants. Appliance, fixation, nail/blade/plate combination, multiple component.
- Recall number
- Z-1825-2016
- Recalling firm
- Biomet, Inc.
- Product
- Various trauma and sports medicine instruments and implants. Appliance, fixation, nail/blade/plate combination, multiple component.
- Status
- Terminated
- Initiated
- 2016-04-01
- Posted
- 2016-05-26
- Terminated
- 2017-05-23
- Reason
- Insufficient seal strength on sterile barrier packaging. The seal could be jeopardized causing the sterile barrier to be compromised and the product could become nonsterile. If the product becomes non-sterile and is used or implanted, it may lead to an infection.
- Root cause
- Equipment maintenance
- Action
- Zimmer Biomet sent an Urgent Medical Device Recall Notice dated April 1, 2016, to all affected customers. Customers were instructed to locate and return the affected product, and implanting surgeons were instructed to monitor patients. The recall notification included a description of the reason for the recall, affected product, consignee responsibilities, and instructions for responding to the formal recall notification. Questions related to this notice should be directed to (574) 372-1570, Monday through Friday, 8 a.m. to 5 p.m.
- Quantity
- not on file
- Distribution
- Worldwide Distribution - US (Nationwide) and globally to Argentina, Australia, Brazil, Canada, Chile, Colombia, Costa Rica, Ecaudor, The Netherlands, Japan, Korea, Malaysia, Mexico, Peru.
- Lot, serial or model codes
- Part #'s 200185 200195 200200 16-235136 Lot #'s 711680 655630 691980 722690 692000 722670 744670
- 510(k) numbers
- ["K964880"]
- PMA numbers
- not on file
- Product code
- KTT
- Firm FEI
- 1825034
- Firm city
- Warsaw
- Firm state
- IN
- Firm country
- not on file
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28