ConMed Corporation Recall: ADULT Radiotransparent Electrode, REF/Catalog Number 2516H, Rx
ConMed Corporation Recall: ADULT Radiotransparent Electrode, REF/Catalog Number 2516H, Rx is one of 9,000 recalls in the RecallGuard dataset. Key details — Recalling firm: ConMed Corporation; Product: ADULT Radiotransparent Electrode, REF/Catalog Number 2516H, Rx ONLY --- COMPARABLE TO PHILIPS MEDICAL HEARTSTART ELECTR
| Recalling firm | ConMed Corporation |
|---|---|
| Product | ADULT Radiotransparent Electrode, REF/Catalog Number 2516H, Rx ONLY --- COMPARABLE TO PHILIPS MEDICAL HEARTSTART ELECTRODES PLUG STYLE CONNECTOR |
| Reason for recall | Philips Healthcare made changes to the design of the connection between multifunction electrodes and their HeartStart FR3 and HeartStart FRx AEDs. The failure to connect may result in a delay of therapy, which could result in patient death or serious injury. |
| Classification | Class I (most serious — reasonable probability of serious health consequences or death) |
| Status | Terminated |
| Distribution | Worldwide Distribution - USA (nationwide) Puerto Rico, and Internationally to Bosnia, Herzegovina, Brazil, Canada, Great Britain, Israel, Italy, Republic of Korea, Norway, Portugal, Saudi Arabia, and Spain. |
| Recall initiated | 20141106 |
| Recall number | Z-0457-2015 |
| Category | device |
| State | NY |
| Country | United States |
$29/mo
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