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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 1 of 13

Device	Model / Reference	Registries	Class	Status
Handicare	280402	FDA UDI	Class I	Active
Handicare	8E4330	FDA UDI	Class I	Active
Handicare	537131	FDA UDI	Class I	Active
Handicare	360980	FDA UDI	Class I	Active
Handicare	8H4500	FDA UDI	Class I	Active
Handicare	8B0700	FDA UDI	Class I	Active
Handicare	8H2731	FDA UDI	Class I	Active
Handicare	8H4601	FDA UDI	Class I	Active
Handicare	400600	FDA UDI	Class I	Active
Handicare	8D1720	FDA UDI	Class I	Active
Handicare	402501	FDA UDI	Class I	Active
Handicare	400003	FDA UDI	Class I	Active
Handicare	323237M	FDA UDI	Class I	Active
Handicare	360931	FDA UDI	Class I	Active
Handicare	547820	FDA UDI	Class I	Active
Handicare	8D1220	FDA UDI	Class I	Active
Handicare	360753	FDA UDI	Class I	Active
Handicare	341502	FDA UDI	Class I	Active
Handicare	537151	FDA UDI	Class I	Active
Handicare	280071	FDA UDI	Class I	Active
Handicare	323103	FDA UDI	Class I	Active
Handicare	402506	FDA UDI	Class I	Active
Handicare	323100	FDA UDI	Class I	Active
Handicare	323602	FDA UDI	Class I	Active
Handicare	450000	FDA UDI	Class I	Active
Handicare	323223	FDA UDI	Class I	Active
Handicare	8A1400	FDA UDI	Class I	Active
Handicare	520547070-2	FDA UDI	Class I	Active
Handicare	8D4430	FDA UDI	Class I	Active
Handicare	8H1300	FDA UDI	Class I	Active
Handicare	329137	FDA UDI	Class I	Active
Handicare	400038	FDA UDI	Class I	Active
Handicare	323102	FDA UDI	Class I	Active
Handicare	537630	FDA UDI	Class I	Active
Handicare	323150	FDA UDI	Class I	Active
Handicare	8H1201	FDA UDI	Class I	Active
Handicare	360404M	FDA UDI	Class I	Active
Handicare	400018	FDA UDI	Class I	Active
Handicare	402465	FDA UDI	Class I	Active
Handicare	5208E4530-B-1	FDA UDI	Class I	Active
Handicare	402513	FDA UDI	Class I	Active
Handicare	329187	FDA UDI	Class I	Active
Handicare	230211	FDA UDI	Class I	Active
Handicare	8A1300	FDA UDI	Class I	Active
Handicare	8D1620	FDA UDI	Class I	Active
Handicare	400102	FDA UDI	Class I	Active
Handicare	8A2700	FDA UDI	Class I	Active
Handicare	402514	FDA UDI	Class I	Active
Handicare	360761	FDA UDI	Class I	Active
Handicare	537105	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.