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Open, Classified

Arjo Portable Scale Adaptor, Model Number 700.05725; accessory intended to be used in combination with compatible patient lifting equipment

FDA Recall Z-1629-2023 · Posted 2023-05-24

Recalling FirmArjohuntleigh Magog, Inc.
Recall StatusOpen, Classified
Product CodeFSA
Date Initiated2023-02-17
Product Quantity3

Reason for Recall

Some Arjo Portable Scale Adaptors have been assembled with straps that have a potential to detach.

Firm Action

Arjo issue an URGENT MEDICAL DEVICE RECALL notice to its consignees on 02/17/2023 via letter, UPS, 2nd Day Delivery. The notice explained the problem, the risk, and requested the consignee remove the units from use and destroy them. The firm will be replacing the units upon receipt of the completed response form. For questions or assistance in completing the Customer Response Form, please contact Arjo at 1 800-323-1245 or via email at [email protected].

Root Cause

Process control

Distribution Pattern

US: OH, NY

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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