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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 9 of 13

Device	Model / Reference	Registries	Class	Status
Handicare	323236	FDA UDI	Class I	Active
Handicare	8H1700	FDA UDI	Class I	Active
Handicare	8H1621	FDA UDI	Class I	Active
Handicare	537610	FDA UDI	Class I	Active
Handicare	8D4530	FDA UDI	Class I	Active
Handicare	520547071	FDA UDI	Class I	Active
Handicare	8H2701	FDA UDI	Class I	Active
Handicare	231007	FDA UDI	Class I	Active
Handicare	8H4230	FDA UDI	Class I	Active
Handicare	323100V	FDA UDI	Class I	Active
Handicare	329191	FDA UDI	Class I	Active
Handicare	323213	FDA UDI	Class I	Active
Handicare	323400	FDA UDI	Class I	Active
Handicare	8H1220	FDA UDI	Class I	Active
Handicare	517420	FDA UDI	Class I	Active
Handicare	8A4530	FDA UDI	Class I	Active
Handicare	537650	FDA UDI	Class I	Active
Handicare	329101	FDA UDI	Class I	Active
Handicare	8A4330	FDA UDI	Class I	Active
Handicare	329100M	FDA UDI	Class I	Active
Handicare	323217M	FDA UDI	Class I	Active
Handicare	8E4702	FDA UDI	Class I	Active
Handicare	400041	FDA UDI	Class I	Active
Handicare	8A2430	FDA UDI	Class I	Active
Handicare	8E4432	FDA UDI	Class I	Active
Handicare	600022	FDA UDI	Class I	Active
Handicare	8H2431	FDA UDI	Class I	Active
Handicare	400077	FDA UDI	Class I	Active
Handicare	507802	FDA UDI	Class I	Active
Handicare	517440	FDA UDI	Class I	Active
Handicare	400011	FDA UDI	Class I	Active
Handicare	303060	FDA UDI	Class I	Unknown
Handicare	8H1721	FDA UDI	Class I	Active
Handicare	323240	FDA UDI	Class I	Active
Handicare	303074	FDA UDI	Class I	Unknown
Handicare	400014	FDA UDI	Class I	Active
Handicare	8D1320	FDA UDI	Class I	Active
Handicare	510428	FDA UDI	Class I	Active
Handicare	323601	FDA UDI	Class I	Active
Handicare	8A1720	FDA UDI	Class I	Active
Handicare	329102	FDA UDI	Class I	Active
Handicare	329151	FDA UDI	Class I	Active
Handicare	517305	FDA UDI	Class I	Active
Handicare	8C0700	FDA UDI	Class I	Active
Handicare	521043	FDA UDI	Class I	Active
Handicare	370840	FDA UDI	Class I	Active
Handicare	329126	FDA UDI	Class I	Active
Handicare	8H1720	FDA UDI	Class I	Active
Handicare	230555	FDA UDI	Class I	Active
Handicare	8H2601	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.