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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 7 of 13

Device	Model / Reference	Registries	Class	Status
Handicare	8H2330	FDA UDI	Class I	Active
Handicare	400006	FDA UDI	Class I	Active
Handicare	8H1500	FDA UDI	Class I	Active
Handicare	8A4600	FDA UDI	Class I	Active
Handicare	370856	FDA UDI	Class I	Active
Handicare	547050	FDA UDI	Class I	Active
Handicare	323237V	FDA UDI	Class I	Active
Handicare	8C0500	FDA UDI	Class I	Active
Handicare	547104	FDA UDI	Class I	Active
Handicare	323242	FDA UDI	Class I	Active
Handicare	5208C0200-B	FDA UDI	Class I	Active
Handicare	400074	FDA UDI	Class I	Active
Handicare	341527	FDA UDI	Class I	Active
Handicare	370849	FDA UDI	Class I	Active
Handicare	450019	FDA UDI	Class I	Active
Handicare	400010	FDA UDI	Class I	Active
Handicare	8A4300	FDA UDI	Class I	Active
Handicare	8H1420	FDA UDI	Class I	Active
Handicare	600017	FDA UDI	Class I	Active
Handicare	507920	FDA UDI	Class I	Active
Handicare	323126M	FDA UDI	Class I	Active
Handicare	323237	FDA UDI	Class I	Active
Handicare	370800	FDA UDI	Class I	Active
Handicare	507816	FDA UDI	Class I	Active
Handicare	400029	FDA UDI	Class I	Active
Handicare	324203	FDA UDI	Class I	Active
Handicare	8E4402	FDA UDI	Class I	Active
Handicare	8C0600	FDA UDI	Class I	Active
Handicare	521041	FDA UDI	Class I	Active
Handicare	547071	FDA UDI	Class I	Active
Handicare	360744	FDA UDI	Class I	Active
Handicare	402508	FDA UDI	Class I	Active
Handicare	8C0200	FDA UDI	Class I	Active
Handicare	510435	FDA UDI	Class I	Active
Handicare	8H2631	FDA UDI	Class I	Active
Handicare	400027	FDA UDI	Class I	Active
Handicare	8H4600	FDA UDI	Class I	Active
Handicare	600084	FDA UDI	Class I	Active
Handicare	507930	FDA UDI	Class I	Active
Handicare	400085	FDA UDI	Class I	Active
Handicare	324206	FDA UDI	Class I	Active
Handicare	547113	FDA UDI	Class I	Active
Handicare	8A1420	FDA UDI	Class I	Active
Handicare	8H1701	FDA UDI	Class I	Active
Handicare	517540	FDA UDI	Class I	Active
Handicare	8B0200	FDA UDI	Class I	Active
Handicare	230500	FDA UDI	Class I	Active
Handicare	537111	FDA UDI	Class I	Active
Handicare	8E4502	FDA UDI	Class I	Active
Handicare	303091	FDA UDI	Class I	Unknown

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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.