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CONMED
Conmed Corporation · Model 130142 · UDI-DI 30653405002103
10
510(k) clearances
59
Adverse events
3
Recalls
33
Facilities
Description
ELECTROSURGICAL FOOTSWITCH COVER
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2012-12-27 | ConMed Corporation | ConMed received complaints of some devices which had broken through the seal of the sterile pouch. ConMed confirmed instances where the pouch seal was compromised on the affected |
| 2003-07-16 | Valleylab, Inc | Pads may have a thin plastic film covering the conductive gel surface underneath the normal printed cover, causing non-adherence and possible burn. |
| 2003-07-16 | Valleylab, Inc | Pads may have a thin plastic film covering the conductive gel surface underneath the normal printed cover, causing non-adherence and possible burn. |
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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.