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HANDICARE USA, INC.

Last updated September 17, 2026

Information

Country: US
Address: 10888 Metro Ct., Maryland Heights, MO, 63043
Website: —
LinkedIn: —
Facebook: —
Email: —
Phone: —
PRRC Contact: —
EUDAMED SRN: —
FDA FEI Number: 3007802293
DUNS Number: 800145836

Catalogue (603)

Page 12 of 13

Device	Model / Reference	Registries	Class	Status
Handicare	400025	FDA UDI	Class I	Active
Handicare	8H4530	FDA UDI	Class I	Active
Handicare	537141	FDA UDI	Class I	Active
Handicare	520517410-B	FDA UDI	Class I	Active
Handicare	517510	FDA UDI	Class I	Active
Handicare	400083	FDA UDI	Class I	Active
Handicare	341517	FDA UDI	Class I	Active
Handicare	323120	FDA UDI	Class I	Active
Handicare	507810	FDA UDI	Class I	Active
Handicare	8D1420	FDA UDI	Class I	Active
Handicare	400602	FDA UDI	Class I	Active
Handicare	520507740-B-1	FDA UDI	Class I	Active
Handicare	8A2330	FDA UDI	Class I	Active
Handicare	517505	FDA UDI	Class I	Active
Handicare	341507	FDA UDI	Class I	Active
Handicare	8A2730	FDA UDI	Class I	Active
Handicare	8E4700	FDA UDI	Class I	Active
Handicare	280076	FDA UDI	Class I	Active
Handicare	370826	FDA UDI	Class I	Active
Handicare	8H2331	FDA UDI	Class I	Active
Handicare	8A1220	FDA UDI	Class I	Active
Handicare	402507	FDA UDI	Class I	Active
Handicare	323600	FDA UDI	Class I	Active
Handicare	341506	FDA UDI	Class I	Active
Handicare	400042	FDA UDI	Class I	Active
Handicare	8A1600	FDA UDI	Class I	Active
Handicare	8E4600	FDA UDI	Class I	Active
Handicare	507807	FDA UDI	Class I	Active
Handicare	8H2500	FDA UDI	Class I	Active
Handicare	323127	FDA UDI	Class I	Active
Handicare	8E4430	FDA UDI	Class I	Active
Handicare	230510	FDA UDI	Class I	Active
Handicare	341400	FDA UDI	Class I	Active
Handicare	324201	FDA UDI	Class I	Active
Handicare	230505	FDA UDI	Class I	Active
Handicare	547115	FDA UDI	Class I	Active
Handicare	280077	FDA UDI	Class I	Active
Handicare	5208H4430-S	FDA UDI	Class I	Active
Handicare	8D4630	FDA UDI	Class I	Active
Handicare	303077	FDA UDI	Class I	Unknown
Handicare	547061	FDA UDI	Class I	Active
Handicare	520537520-S-2	FDA UDI	Class I	Active
Handicare	517340	FDA UDI	Class I	Active
Handicare	547810XXL	FDA UDI	Class I	Active
Handicare	520507818-M	FDA UDI	Class I	Active
Handicare	510426	FDA UDI	Class I	Active
Handicare	329153	FDA UDI	Class I	Active
Handicare	400040	FDA UDI	Class I	Active
Handicare	323126	FDA UDI	Class I	Active
Handicare	8E4201	FDA UDI	Class I	Active

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FDA Recalls (5)

Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.

Date	Recall No.	Class	Status	Reason
Nov 3, 2017	Z-2753-2018	—	terminated	Premature strap wear and breakage at maximum weight conditions (625 lbs.).
Nov 3, 2017	Z-2752-2018	—	terminated	Premature strap wear and breakage at maximum weight conditions (625 lbs.).
Sep 8, 2017	Z-0013-2018	—	terminated	During internal cycle testing of A-Series lifts Handicare has found that the A-Series lift strap for lifts manufactured between April 25, 2017 and June 12, 2017 may wear prematurely at max load (625 lbs). We have identified the root cause as a supplied component that was not to specification. If the strap wears during use there is a potential risk for the person being supported by the lift to drop.
Mar 26, 2015	Z-1613-2015	—	terminated	Complaints were received that the heat-welded seam on the wipeable belt's strap tore when force was applied.
Apr 15, 2014	Z-0303-2017	—	terminated	During the period of April 2009 May 2011, Handicare AB used a wing handle in which the screw and handle, after repeated tightening, may slide apart. This causes a small amount of play in the attachment of the ladder, which in turn results in high load at the attachment holes of the ladder. Eventually, this may cause mechanical fatigue in the material of the ladder.