PADPRO ADULT Radiotranslucent Pad w/Medtronic connector… recallZ-0757-2007 · Conmed Corporation · initiated Mar 8, 2007
Terminated All recalls posted in April 2007
Is my device affected?
- Compare the model, catalog and lot or serial numbers on your device or its packaging with the code information below. A recall usually covers only specific models or lots.
- If yours is listed, follow the instructions from Conmed Corporation or your healthcare provider. The company's action is summarized under what the company is doing.
- Do not stop using a prescribed or implanted device on your own — talk to your healthcare provider first.
Where to find your model and lot numbers · What recall classes and statuses mean
Why it was recalled
Firm was notified of three incidents over the past 15 months in which customers opened the pouch & found an incorrect connector. This error makes the product unusable. The Zoll and Medtronic connectors are not interchangeable and are unique to their specific device.
FDA root cause category: Other
What the company is doing
On 3/08/07, "URGENT DEVICE RECALL" letters (dated 3/05/07) will be sent via UPS to the US distributors and direct user accounts. The letters inform them of the problem and of the recall. The letters instruct them to immediately discontinue using the affected lots, inspect their stocks, and to return them as soon as possible. The letters instruct the consignees to notify their customers of the recall of the devices to the user level if they have been distributed, and request the return of the products. Additionally, when requested, ConMed will notify distributor's customers (sub-accounts) by the same means. Returned devices will be automatically replaced by ConMed Corporation. A separate letter is being sent to the foreign accounts today instructing them to return the devices back to ConMed Corporation for final disposition. The letters also instruct the consignees to complete the accompanying reply form and fax it to Nancy Crisino at (315) 624-3089. ConMed has contracted Stericycle in Indianapolis, IN, to handle the recall and returns from the domestic accounts.
Recall details
- Recall number
- Z-0757-2007
- Recall class
- Not yet classified by the FDA
- Status
- Terminated
- Initiated by the company
- Mar 8, 2007
- Posted by the FDA
- Apr 24, 2007
- Recalling firm
- Conmed Corporation
- Quantity
- 920 pairs
- Product code
- MLN
- FDA submissions
- K020203
- Distribution
- Worldwide, including USA, Canada, Romania, Chile, and Belgium
Product description
PADPRO ADULT Radiotranslucent Pad w/Medtronic connector, REF/Catalog #2516M. RX ONLY. Defibrillation/Pacing/Cardioversion/Monitoring Electrodes. Made in USA for: CONMED CORPORATION Utica, New York, 13502.
Code information (models, lots, serial numbers)
Lot Y101105-4
Other devices under the same FDA submission
3 devices cleared under K020203 — the recall does not name any of them by identifier. One submission often covers many models, so they may or may not be affected.
- PadPro 2516MConmed Corporation · Automated External Defibrillators (Non-Wearable)6 reports
- PadPro 2516M-PCConmed Corporation · Automated External Defibrillators (Non-Wearable)2 reports
- PadPro 2516ZConmed Corporation · Automated External Defibrillators (Non-Wearable)1 report
Other products in the same recall event
The FDA groups related products into one recall event (event 37495).
- Z-0756-2007 · TerminatedPADPRO ADULT Radiotranslucent Pad w/Zoll connector. Defibrillation/Pacing/Cardioversion/Monitoring Electrodes, REF/Catalog # 2516Z. RX ONLY. Made in USA for: CONMED CORPORATION Uti…
Sources and updates
- Recall record: FDA Medical Device Recalls, file dated Oct 16, 2026 · View the FDA recall notice ↗
- Devices: FDA GUDID, file dated Oct 13, 2026. Devices are linked when their identifier (with a valid check digit) appears in the recall's code information.
- Page last rebuilt: Oct 18, 2026. Text above is shown as published by the FDA.
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