Health product recall

Overhead Lift Roomer S and Altair (2016-07-07)

Starting date:
July 7, 2016
Posting date:
October 19, 2018
Type of communication:
Medical Device Recall
Subcategory:
Medical Device
Hazard classification:
Type III
Source of recall:
Health Canada
Issue:
Medical Devices
Audience:
General Public, Healthcare Professionals, Hospitals
Identification number:
RA-67956

Affected products

  1. Overhead lift Roomer S
  2. Overhead lift Altair

Reason

A field safety notice concerning overhead lifts.

Affected products

A. Overhead lift Roomer S

Lot or serial number

More than 10 numbers, contact manufacturer.

Model or catalog number
  • 55200-NA
  • 55210-NA
  • 55220-NA
  • 55300-NA
Companies
Manufacturer

HUMAN CARE HC SWEDEN AB

ARSTAANGSVAGEN 21C

STOCKHOLM

11743

SWEDEN

B. Overhead lift Altair

Lot or serial number

More than 10 numbers, contact manufacturer.

Model or catalog number

55200-NA
55210-NA
55220-NA
55300-NA

Companies
Manufacturer

HUMAN CARE HC SWEDEN AB

ARSTAANGSVAGEN 21C

STOCKHOLM

11743

SWEDEN