Arjohuntleigh Magog, Inc. Arjo Portable Scale Adaptor, Model Number 700.05725; accessory intended to be used in combination with compatible patient lifting equipment Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Arjo Portable Scale Adaptor, Model Number 700.05725; accessory intended to be used in combination with compatible patient lifting equipment
Brand
Arjohuntleigh Magog, Inc.
Lot Codes / Batch Numbers
UDI/DI 05055982760713, Serial Numbers: 300501841, 300501842, 300515661
Products Sold
UDI/DI 05055982760713, Serial Numbers: 300501841, 300501842, 300515661
Arjohuntleigh Magog, Inc. is recalling Arjo Portable Scale Adaptor, Model Number 700.05725; accessory intended to be used in combination wi due to Some Arjo Portable Scale Adaptors have been assembled with straps that have a potential to detach.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Some Arjo Portable Scale Adaptors have been assembled with straps that have a potential to detach.
Recommended Action
Per FDA guidance
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 ArjoCustomer.Response-US@arjo.com.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
NY, OH
Page updated: Jan 10, 2026