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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 3 of 13

Device	Model / Reference	Registries	Class	Status
Handicare	520517505-1	FDA UDI	Class I	Active
Handicare	600020	FDA UDI	Class I	Active
Handicare	450005	FDA UDI	Class I	Active
Handicare	8A2530	FDA UDI	Class I	Active
Handicare	400022	FDA UDI	Class I	Active
Handicare	8A1500	FDA UDI	Class I	Active
Handicare	510431	FDA UDI	Class I	Active
Handicare	527350	FDA UDI	Class I	Active
Handicare	520547070-1	FDA UDI	Class I	Active
Handicare	8A4630	FDA UDI	Class I	Active
Handicare	400080	FDA UDI	Class I	Active
Handicare	600072	FDA UDI	Class I	Active
Handicare	323126Q	FDA UDI	Class I	Active
Handicare	303090	FDA UDI	Class I	Unknown
Handicare	323626	FDA UDI	Class I	Active
Handicare	600210	FDA UDI	Class I	Active
Handicare	230020	FDA UDI	Class I	Active
Handicare	230100	FDA UDI	Class I	Active
Handicare	8E4332	FDA UDI	Class I	Active
Handicare	510424	FDA UDI	Class I	Active
Handicare	8H4730	FDA UDI	Class I	Active
Handicare	323245	FDA UDI	Class I	Active
Handicare	547070	FDA UDI	Class I	Active
Handicare	280401	FDA UDI	Class I	Active
Handicare	8B0600	FDA UDI	Class I	Active
Handicare	600078	FDA UDI	Class I	Active
Handicare	8H4231	FDA UDI	Class I	Active
Handicare	8E4401	FDA UDI	Class I	Active
Handicare	8A1320	FDA UDI	Class I	Active
Handicare	8H4430	FDA UDI	Class I	Active
Handicare	8E4601	FDA UDI	Class I	Active
Handicare	323117V	FDA UDI	Class I	Active
Handicare	400028	FDA UDI	Class I	Active
Handicare	8E4530	FDA UDI	Class I	Active
Handicare	517530	FDA UDI	Class I	Active
Handicare	400020	FDA UDI	Class I	Active
Handicare	280074	FDA UDI	Class I	Active
Handicare	402450	FDA UDI	Class I	Active
Handicare	341526	FDA UDI	Class I	Active
Handicare	341500	FDA UDI	Class I	Active
Handicare	8H2730	FDA UDI	Class I	Active
Handicare	507817	FDA UDI	Class I	Active
Handicare	8E4631	FDA UDI	Class I	Active
Handicare	360986	FDA UDI	Class I	Active
Handicare	323241	FDA UDI	Class I	Active
Handicare	400046	FDA UDI	Class I	Active
Handicare	517410	FDA UDI	Class I	Active
Handicare	400072	FDA UDI	Class I	Active
Handicare	600030	FDA UDI	Class I	Active
Handicare	521042	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.