This page has been archived on the Web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.
35X Proflexx Complete (2014-12-02)
- Starting date:
- December 2, 2014
- Posting date:
- December 23, 2014
- Type of communication:
- Medical Device Recall
- Subcategory:
- Medical Device
- Hazard classification:
- Type II
- Source of recall:
- Health Canada
- Issue:
- Medical Devices
- Audience:
- General Public, Healthcare Professionals, Hospitals
- Identification number:
- RA-43003
Recalled Products
35X Proflexx Complete
Reason
Potential issue that may involve the threaded shank of the wheel caster assembly of the 35X Proflexx Cot.
Affected products
35X Proflexx Complete
Lot or serial number
More than 10 numbers, contact manufacturer.
Model or catalog number
001-5690, 001-5691-NS, 001-5692, 001-5693R, 001-5698
Companies
- Manufacturer
-
Ferno,Division of Ferno-Washington Inc.
Ferno-Washington Inc.
70 Weil Way,
Wilmington
45177
Ohio
UNITED STATES