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Drive Devilbiss Healthcare · Model 735-135 · UDI-DI 07540212152256
INP
Prescription
8
510(k) clearances
339
Adverse events
9
Recalls
143
Facilities
Description
CANETIP 7/8" BLACK, 6EA/CV, 24EA/CT, Ret
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2016-02-17 | Medical Depot Inc. | Tip crutch failure involving the bottom of the metal portion which comes in contact with ground |
| 2016-02-17 | Medical Depot Inc. | Tip crutch failure involving the bottom of the metal portion which comes in contact with ground |
| 2016-02-17 | Medical Depot Inc. | Tip crutch failure involving the bottom of the metal portion which comes in contact with ground |
| 2016-02-17 | Medical Depot Inc. | Tip crutch failure involving the bottom of the metal portion which comes in contact with ground |
| 2016-02-17 | Medical Depot Inc. | Tip crutch failure involving the bottom of the metal portion which comes in contact with ground |
| 2016-02-17 | Medical Depot Inc. | Tip crutch failure involving the bottom of the metal portion which comes in contact with ground |
| 2004-08-04 | Duro-Med Industries, Inc. | The crutches were labeled as latex free, but contain rubber in the hand grips, tips and underarm padding of the crutches. |
| 2004-08-04 | Duro-Med Industries, Inc. | The crutches were labeled as latex free, but contain rubber in the hand grips, tips and underarm padding of the crutches. |
| 2004-08-04 | Duro-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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Get your free API keyRead the docsData 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.