Recall Z-1629-2023— Arjohuntleigh Magog, Inc.
Class II · Ongoing
Class II FDA medical device recall by Arjohuntleigh Magog, Inc., initiated 2023-02-17. FDA's recall record names no specific 510(k) clearance for this event. Product: Arjo Portable Scale Adaptor, Model Number 700.05725; accessory intended to be used in combination with compatible patient lifting equipment. Reason: Some Arjo Portable Scale Adaptors have been assembled with straps that have a potential to detach..
- Recalling firm
- Arjohuntleigh Magog, Inc.
- Classification
- Class II
- Status
- Ongoing
- Initiated
- 2023-02-17
- Firm location
- Magog, N/A, Canada
Product description
Arjo Portable Scale Adaptor, Model Number 700.05725; accessory intended to be used in combination with compatible patient lifting equipment
Reason for recall
Some Arjo Portable Scale Adaptors have been assembled with straps that have a potential to detach.
Data sourced from openFDA. This site is unofficial and independent of the FDA.