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Assembly Required Distributors Inc.

Assembly Required Distributors Inc · Model CHM8908-01 · UDI-DI 00860004575627

INP
8
510(k) clearances
340
Adverse events
9
Recalls
143
Facilities

Description

Doctor Stool Replacement Rubber Tip

Recalls

DateFirmReason
2016-02-17Medical Depot Inc.Tip crutch failure involving the bottom of the metal portion which comes in contact with ground
2016-02-17Medical Depot Inc.Tip crutch failure involving the bottom of the metal portion which comes in contact with ground
2016-02-17Medical Depot Inc.Tip crutch failure involving the bottom of the metal portion which comes in contact with ground
2016-02-17Medical Depot Inc.Tip crutch failure involving the bottom of the metal portion which comes in contact with ground
2016-02-17Medical Depot Inc.Tip crutch failure involving the bottom of the metal portion which comes in contact with ground
2016-02-17Medical Depot Inc.Tip crutch failure involving the bottom of the metal portion which comes in contact with ground
2004-08-04Duro-Med Industries, Inc.The crutches were labeled as latex free, but contain rubber in the hand grips, tips and underarm padding of the crutches.
2004-08-04Duro-Med Industries, Inc.The crutches were labeled as latex free, but contain rubber in the hand grips, tips and underarm padding of the crutches.
2004-08-04Duro-Med Industries, Inc.The crutches were labeled as latex free, but contain rubber in the hand grips, tips and underarm padding of the crutches.

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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.