The Recall Desk
HighFDA (Devices)·Z-1629-2023·Announced 2023-05-31

Arjo Portable Scale Adaptor Model 700.05725 Recalled for Potential Strap Detachment

Arjohuntleigh Magog, Inc. is recalling certain Arjo Portable Scale Adaptors due to straps with potential to detach. Three units were distributed in Ohio and New York.

What this means for you

Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.

Our severity reasoning: This is classified as FDA Class II with a potential risk of harm from strap detachment during patient lifting operations. No injuries or illnesses have been reported to date. Per the severity rubric, risk-of-harm products without reported injury are rated as High (3).

Plain-English summary

Arjohuntleigh Magog, Inc. is recalling certain Arjo Portable Scale Adaptors, Model Number 700.05725. This device is an accessory designed for use with compatible patient lifting equipment.

The U.S. Food and Drug Administration has classified this as a Class II recall. The agency determined that some units have been assembled with straps that have a potential to detach.

Three units bearing serial numbers 300501841, 300501842, and 300515661 have been identified as affected. These units were distributed in Ohio and New York.

The recalled product

Product
Arjo Portable Scale Adaptor, Model Number 700.05725; accessory intended to be used in combination with compatible patient lifting equipment
Manufacturer
Arjohuntleigh Magog, Inc.
Category
Medical Device — Patient Lifting Equipment Accessory
Hazard
Affected units
3

Is your product affected?

Check your packaging against the codes below. If any of them match, the product is part of this recall.

Lot numbers (4)

  • UDI/DI 05055982760713
  • Serial Numbers: 300501841
  • 300501842
  • 300515661

Distribution

Distributed in 2 states:

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Same manufacturer · Arjohuntleigh Magog, Inc.

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Same hazard · strap detachment

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