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Molded J&L

Therafin Corporation · Model 51104 · UDI-DI 00840252927508

KNO
10
510(k) clearances
67
Adverse events (4 deaths)
3
Recalls
220
Facilities

Description

BACK HDWR, 2 MOLDED J&L W/ SWINGTABS & 3" RISE 3" DEPTH HINGE

Recalls

DateFirmReason
2020-03-02Merits Holdings Co. dba Merits Health Products, Inc.Pinion gear may disengage from track allowing lift to slip or jolt.
2004-02-02Action Products IncorporatedWheelchair seat may not properly support the user due to cracks in the plastic seat base.
2002-05-14Action Products IncorporatedWheelchair seat component is defective.

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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.