FDA Device recall Z-1949-2012

Sara Plus Mobile Patient Lifter

FDA Device
Class II
terminated
Published 2012-07-18

On 2012-07-18 the FDA classified a Class II recall of Sara Plus Mobile Patient Lifter by Arjo, citing 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.

Read the official FDA Device notice

Agency	FDA Device
Recall number	Z-1949-2012
Classification	Class II
Status	terminated
Initiated	2012-06-29
Published	2012-07-18
Last updated	2026-09-13 11:53 UTC
Company	Arjo
Distribution	US

Product

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.

Reason

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.

Identifiers

code_info	Models HEP0001-US, serial numbers SPSN0808U285, PN1010U507, PN1102U092, PN1102U110, SPSN0905U022, SPSN0907U048, SPSN090… Models HEP0001-US, serial numbers SPSN0808U285, PN1010U507, PN1102U092, PN1102U110, SPSN0905U022, SPSN0907U048, SPSN0909U091, SPSN0605U388, SPSN0810U506, PN1102U093, PN1102U101, PN1102U112, PN1104U199, PN1104U201, PN1104U203, PN1104U214, PN1104U215, PN1104U216, PN1104U217, PN1104U220, PN1104U224, PN1104U225, PN1106U365, SPSN0804U387, 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, PN1009U430, PN1008U393, SPSN0904U419, SPSN0906U038, SPSN0605U138, SPSN0605U140, SPSN0605U145, SPSN0605U148, SP

code_info

Models HEP0001-US, serial numbers SPSN0808U285, PN1010U507, PN1102U092, PN1102U110, SPSN0905U022, SPSN0907U048, SPSN090…

Models HEP0001-US, serial numbers SPSN0808U285, PN1010U507, PN1102U092, PN1102U110, SPSN0905U022, SPSN0907U048, SPSN0909U091, SPSN0605U388, SPSN0810U506, PN1102U093, PN1102U101, PN1102U112, PN1104U199, PN1104U201, PN1104U203, PN1104U214, PN1104U215, PN1104U216, PN1104U217, PN1104U220, PN1104U224, PN1104U225, PN1106U365, SPSN0804U387, 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, PN1009U430, PN1008U393, SPSN0904U419, SPSN0906U038, SPSN0605U138, SPSN0605U140, SPSN0605U145, SPSN0605U148, SP

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1949-2012%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.