Lead Adaptor Bipolar/Unipolar BLV/BIS-40Recalls & reported problems
Oscor Inc. · Class 2 · Implant
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00836559006428), received between Dec 4, 2018 and Dec 4, 2018 — classified as 1 malfunction.
The most frequently reported specific device problem is “Device Markings/Labelling Problem” (1 report).
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Most reported problems
Device problems
- Device Markings/Labelling Problem1
Patient problems
- No Patient Involvement1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionDec 4, 2018Device Markings/Labelling Problem; Device Markings/Labelling Problem
IT WAS REPORTED THAT THE LEAD ADAPTER WAS SHIPPED WITH ITS PACKAGING NOTING ONE EXPIRATION DATE, AND THE SYSTEM NOTING A DIFFERENT EXPIRATION DATE. THE PRODUCT WAS NOT USED. THERE WAS NO PATIENT INVOLVEMENT.
Patient problems: No Patient Involvement
MAUDE report 8129804 ↗
Other Pacemaker Lead Adaptor devices
- Introducer Kit for Impella® 0052-3006Oscor Inc. · pacemaker lead Adaptor4 recalls223 deaths1,184 reports
- NA 5867-3MMedtronic, Inc. · pacemaker lead Adaptor25 reports
- Introducer Kit for Impella® 0052-3000Oscor Inc. · pacemaker lead Adaptor2 deaths19 reports
- Lead Adaptor BIS/BIS-40Oscor Inc. · pacemaker lead Adaptor14 reports
- NA 5866-38MMedtronic, Inc. · pacemaker lead Adaptor12 reports
- Lead Adapter 501206Greatbatch Ltd · Pacemaker Lead Adaptor10 reports
- NA 5867-3MMedtronic, Inc. · pacemaker lead Adaptor10 reports
- Lead Adapter 501214Greatbatch Ltd · Pacemaker Lead Adaptor9 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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