Magog, Quebec, Canada
Arjohuntleigh Magog recalls
5 recalls recorded since 2018, most recently on 17 February 2023. 1 is listed as ongoing. Status and classification are as published by the FDA.
Recalls5
Ongoing (FDA)1
Terminated or completed4
Class I (FDA)0
Ongoing Class II Medical devices
- Recall started
- 17 February 2023
- Reason
- Some Arjo Portable Scale Adaptors have been assembled with straps that have a potential to detach.
- Distribution
- US: OH, NY
- Initiated
- Voluntary: Firm initiated
- Recall number
- Z-1629-2023
- Arjo Portable Scale Adaptor, Model Number 700.05725; accessory intended to be used in combination with compatible patient lifting equipment
Terminated Class II Medical devices
- Recall started
- 4 March 2021
- Terminated
- 12 January 2024
- Reason
- The spreader bar can disconnect from the scale bottom attachment.
- Distribution
- Distribution in US - AZ, CA, CO, IL, LA, MA, MI, MO, OH, PA, WA
- Initiated
- Voluntary: Firm initiated
- Recall number
- Z-2479-2021
- Maxi Sky 1000 (Arjo) and V10 (BHM) Bariatric Ceiling Rail - Mounted Lift with measuring function
Terminated Class II Medical devices
- Recall started
- 6 October 2020
- Terminated
- 23 July 2025
- Reason
- Risk of Sling Clip breakage while in use with obsolete Flat Dynamic Positioning System (DPS)
- Distribution
- Worldwide distribution - US Nationwide distribution including in the states of AK, AL, AR, AZ, CA, CO, CT, DC, DE, GA, IA, ID, IL, IN, KS, KY, LA, MI, MN, MO, MS, MT, NC, NE, NH, NY, OH, OK, SC, SD, TN, TX, UT, VA, WI and the countries of Australia, Belgium, Canada, Czech Republic, France, Italy and
- Initiated
- Voluntary: Firm initiated
- Recall number
- Z-1100-2021
- Arjo Flat Dynamic Positioning System (DPS) - Product Usage: used in conjunction with passive clip slings is designed for resident transfer in a homecare setting, at nursing homes and other assisted living centers. Please
Terminated Class II Medical devices
- Recall started
- 19 December 2018
- Terminated
- 26 January 2022
- Reason
- Inability or difficulty in unbuckling/releasing the proning arm buckle might delay patient access in an emergency situation such as cardiac arrest. This, in turn, could contribute to a life-threatening event.
- Distribution
- US, Saudi Arabia, and Kuwait
- Initiated
- Voluntary: Firm initiated
- Recall number
- Z-0802-2019
- ARJOHUNTLEIGH GETINGE GROUP, RotoProne Therapy System, Model Number 209800
Terminated Class II Medical devices
- Recall started
- 12 February 2018
- Terminated
- 20 August 2020
- Reason
- The spreader bar can detach from the scale attachment under certain conditions.
- Distribution
- Worldwide distribution: US (nationwide) to states of: CO, FL, IA, IL, KY, MN, NY, PH, and WA; and countries of: Australia, Belgium, Brazil, Canada, China, France, Germany, Hong Kong, Ireland, Italy, Japan, Netherlands, Norway, Singapore, Swiss, Turkey, United Kingdom, and United Arab Emirates.
- Initiated
- Voluntary: Firm initiated
- Recall numbers
- Z-2661-2018, Z-2660-2018
- Q-Connect 272 KG Scale used with Maxi Sky 2 ceiling lift The Scale is intended to be used with patient lifters to measure the weight of a patient who cannot stand on a scale. It is designed to be used indoors in hospi
- Quick Connect 272 KG Scale used with Maxi Sky 2 ceiling lift The Scale is intended to be used with patient lifters to measure the weight of a patient who cannot stand on a scale. It is designed to be used indoors in h
A terminated FDA recall means the FDA has determined that all reasonable efforts to remove or correct the product have been made. What statuses mean.