This page has been archived on the Web
Information identified as archived is provided for reference, research or recordkeeping purposes. It is not subject to the Government of Canada Web Standards and has not been altered or updated since it was archived. Please contact us to request a format other than those available.
ZIMMER PERIARTICULAR LOCKING PLATE (2016-01-04)
- Starting date:
- January 4, 2016
- Posting date:
- January 22, 2016
- Type of communication:
- Medical Device Recall
- Subcategory:
- Medical Device
- Source of recall:
- Health Canada
- Issue:
- Medical Devices
- Audience:
- General Public, Healthcare Professionals, Hospitals
- Identification number:
- RA-56742
Affected Products
- PERIARTICULAR LOCKING SYSTEM SCREW,58MM
- PERIARTICULAR LOCKING PLATE SYSTEM - 2.4MM LOCKING SCREWS - SS
Reason
Zimmer Biomet is initiating a recall of non-sterile locking plate screws as it was found through a review of complaints that the product on the package label did not match what was inside the package. The label was for part number 00-2359-058-35 (a 58mm length screw) while the product inside the package was part number 00-2359-014-24 (a 14mm length screw).
Affected products
A. PERIARTICULAR LOCKING SYSTEM SCREW,58MM
Lot or serial number
62918019
Model or catalog number
00-2359-058-35
Companies
- Manufacturer
-
Zimmer Inc.
1800 West Center Street
Warsaw
46580
UNITED STATES
B. PERIARTICULAR LOCKING PLATE SYSTEM - 2.4MM LOCKING SCREWS - SS
Lot or serial number
62896038
Model or catalog number
00-2359-014-24
Companies
- Manufacturer
-
Zimmer Inc.
1800 West Center Street
Warsaw
46580
UNITED STATES