FDA Medical Device Recalls (openFDA)
Biomet, Inc.: Vision RingLoc Shell 50 mm Size 23. Hip joint replacement prosthesis.
- Recall number
- Z-2483-2015
- Recalling firm
- Biomet, Inc.
- Product
- Vision RingLoc Shell 50 mm Size 23. Hip joint replacement prosthesis.
- Status
- Terminated
- Initiated
- 2015-07-28
- Posted
- 2015-08-29
- Terminated
- 2016-05-17
- Reason
- The device was assembled without screw hole plugs.
- Root cause
- Under Investigation by firm
- Action
- Zimmer Biomet issued notices on July 28, 2015, via FedEx overnight mail and e-mail to customers. Customers were asked to return response forms and recalled devices to Zimmer Biomet. Customers with questions may call Seth Pixton, Field Action Specialist, at 574-372-1570, Monday through Friday from 8:00 am to 5:00 pm, or e-mail at: seth.pixton@zimmerbiomet.com.
- Quantity
- 5
- Distribution
- Distributed in Canada and Japan.
- Lot, serial or model codes
- Part Number:135250; Lot Number:946410
- 510(k) numbers
- ["K093235"]
- PMA numbers
- not on file
- Product code
- LPH
- 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