Home › Thomas Hilfen für Körperbehinderte GmbH & Co. Medico Kommanditgesellschaft › EASyS Modular S model 22 size 1 Crash

EASyS Modular S model 22 size 1 Crash

Thomas Hilfen für Körperbehinderte GmbH & Co. Medico Kommanditgesellschaft · Model 9800062082000 · UDI-DI 04034089088075

INN

510(k) clearances

586

Adverse events (10 deaths)

Recalls

137

Facilities

Recalls

Date	Firm	Reason
2026-01-05	Raz Design Inc	Due to a modification by a vendor and may be reinstalled without properly engaging the outside rear seat brackets that are used to keep the seat in place.
2022-11-30	Altimate Medical, Inc.	Device manufactured with a component with affects the foldability of the frame, not allowing it to be secured by the frame strap in the folded position.
2021-12-08	R82 A/S	The chrome surface of the push brace can crack during use, potentially cutting the user.
2021-05-12	Stryker Medical Division of Stryker Corporation	Medical devices intended for use in a healthcare facility were distributed to residential customers and may be in use in a home environment. The product s labeling accurately iden
2015-04-02	Winco Mfg., LLC	Shipment of foam for chairs was received classified as Fire Retardant but was in fact standard foam and would not meet Fire Retardant standards.
2015-04-02	Winco Mfg., LLC	Shipment of foam for chairs was received classified as Fire Retardant but was in fact standard foam and would not meet Fire Retardant standards.
2015-04-02	Winco Mfg., LLC	Shipment of foam for chairs was received classified as Fire Retardant but was in fact standard foam and would not meet Fire Retardant standards.
2015-04-02	Winco Mfg., LLC	Shipment of foam for chairs was received classified as Fire Retardant but was in fact standard foam and would not meet Fire Retardant standards.
2015-04-02	Winco Mfg., LLC	Shipment of foam for chairs was received classified as Fire Retardant but was in fact standard foam and would not meet Fire Retardant standards.
2015-04-02	Winco Mfg., LLC	Shipment of foam for chairs was received classified as Fire Retardant but was in fact standard foam and would not meet Fire Retardant standards.

Query this across every FDA database — by API.

Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

Get your free API key Read the docs

Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.