Skip to the content

FDA Medical Device Recalls (openFDA)

Arjohuntleigh Magog, Inc.: 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 note that the DPS can be utilized only if affixed to ceiling lift or passive floor lift.

Recall number
Z-1100-2021
Recalling firm
Arjohuntleigh Magog, Inc.
Product
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 note that the DPS can be utilized only if affixed to ceiling lift or passive floor lift.
Status
Terminated
Initiated
2020-10-06
Posted
not on file
Terminated
2025-07-23
Reason
Risk of Sling Clip breakage while in use with obsolete Flat Dynamic Positioning System (DPS)
Root cause
Nonconforming Material/Component
Action
On 10/06/2020, the firm sent a letter to its consignees with the following instructions. Arjo has become aware that there is a likelihood that a sling clip may break (Image 2) when used with the models of spreader bars referenced above that are out of their lifespan (see note 1 below). The continued use of the obsoleted DPS can lead to complete clip breakage and subsequently to its detachment from the DPS attachment point. As a consequence, the resident may fall off and potentially sustain serious injuries as a consequence. Arjo is taking this matter very seriously and recommends replacement of the obsoleted DPS on ceiling lift or floor lift systems. Note 1: The probability of the event may increase if the DPS is used with a Clip Sling that has exceeded its expected lifespan of 2 years or more than 1.5 years for Passive Clip Slings models MAA2080M, MAA2050M, MAA2040M, MAA2070M and MLAAS2000. Next Steps 1. Verify whether you possess DPS within the range of this Notice and ensure that all caregivers and users of Arjo ceiling lift or floor lifts are made aware of this Field Safety Notice (FSN). 2. Complete and sign the enclosed Customer Response Form and return this document to your local Arjo office. Contact your local Arjo office to take the appropriate decision regarding your obsolete device(s) and select the best solution for your needs. NOTE: Until you find with our Arjo representative the most appropriate solution for your patient transfer needs, the device may stay in use strictly if those two conditions are fulfilled; A. Before each patient transfer, ensure to follow the recommendation of the Sling Instruction for Use and check all parts of the sling are free of any damage B. Ensure the sling used is within its intended lifetime (2 years or 1.5 years for Passive Clip Slings models MAA2080M, MAA2050M, MAA2040M, MAA2070M and MLAAS2000). In addition, if the label of the sling is faded, unreadable or damaged, ensure sling disposal as recomme
Quantity
3390 units
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 Poland.
Lot, serial or model codes
LBA1030-xx, LCA80563-xx, LCA81695-xx, KTX01440.xx, LBX05420-xx, LBX1033-xx, KTS0010
510(k) numbers
not on file
PMA numbers
not on file
Product code
FSA
Firm FEI
3002655016
Firm city
Magog
Firm state
not on file
Firm country
Canada

Where this comes from

Register
FDA Medical Device Recalls (openFDA)
Publisher
U.S. Food and Drug Administration (openFDA)
File
device-recall-0001-of-0001.json.zip
sha256
b87518bfe2e8
Size
288210821 bytes
Published
2026-09-28
Read
2026-09-29T08:25:23.626Z
Source file
Source file retained · verify
Refresh due
2026-10-06

Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.

Cite as

FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28

Search this register