Reported Jul 18, 2012 · Terminated

Sara Plus Mobile Patient Lifter; manufactured for Arjo by Medibo Medical Products N.V., Heikant 5, B-3930 Hamont-Achel,…

Arjo, Inc. dba ArjoHuntleigh

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Arjo, Inc. dba ArjoHuntleigh · 2349 W Lake St · Addison, IL · 60101-6183

Is this the product you have?

  • Sara Plus Mobile Patient Lifter; manufactured for Arjo by Medibo Medical Products N.V., Heikant 5, B-3930 Hamont-Achel, Belgium; Models HEP0001-US and HEP1001-US. The Sara Plus is a standing and raising aid for short transfers e.g. raising from bed and transfer to wheelchair, or from wheelchair to toilet. Sara Plus is also suitable for walking training when the footboard and kneepad are removed.
Lot codes and dates

217 of 217 products

Products covered by this recall
Model / numberProduct as published
1010U507
1102U092
1102U110SPSN0905U022, SPSN0907U048, SPSN0909U091, SPSN0605U388, SPSN0810U506
1102U093
1102U101
1102U112
1104U199
1104U201
1104U203
1104U214
1104U215
1104U216
1104U217
1104U220
1104U224
1104U225
1106U365SPSN0804U387, SPSN0605U421, SPSN0605U423, SPSN0605U425, SPSN0605U431, SPSN0605U432, SPSN0605U440, SPSN0605U199, SPSN0605U365, SPSN0901U033, SPSN0605U206, SPSN0605U214, SPSN0605U217, SPSN0605U220, SPSN0801U071, SPSN0801U072, SPSN0707U484, SPSN0709U689, SPSN0709U692, SPSN0709U693, SPSN0710U842, P0129686, P0123033, SPSN0808U284, P0120989, SPSN0703U140, P0116656, SPSN0605U241, SPSN0605U242, SPSN0605U243, SPSN0605U244, SPSN0605U245, SPSN0605U246, SPSN0605U247, SPSN0605U248, SPSN0605U249, SPSN0605U350, SPSN0605U351, SPSN0605U352, SPSN0605U353, SPSN0808U199
1009U430
1008U393SPSN0904U419, SPSN0906U038, SPSN0605U138, SPSN0605U140, SPSN0605U145, SPSN0605U148, SPSN0605U153, SPSN0605U414, SPSN0605U416, SPSN0605U420, P0121743, SPNS0706U431, SPNS0706U433, SPNS0706U443, SPNS0706U445, SPSN0605U412, SPSN0605U442, SPSN0605U447, SPSN0605U451, SPSN0605U461, SPSN0605U469, SPSN0605U473, SPSN0605U480, SPSN0704U296, SPSN0704U297, SPSN0704U300, SPSN0704U301, SPSN0709U767, SPSN 907U052, SPSN0705U398
1101U039P0122276, SPSN0605U355, SPSN0605U356, SPSN0605U373, SPSN0605U375
Amount recalled
2480 units in U.S., 2,651 units in the rest of the world

This recall covers 3 products

The agency filed one notice per product. You are reading one of them; the other 2 are below.

Where it was sold

  • Nationwide

Why it was recalled

ArjoHuntleigh has received a limited number of customer reports concerning injuries related to an exposed metal support bracket when the proactive knee pad assembly is removed.

This product could cause temporary or reversible health problems — stop using it.

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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Notice updated Mar 13, 2018 · Data as of Sep 19, 6:10 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.