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NA 2872Recalls & reported problems

Medtronic, Inc. · ACCESSORY 2872 ADPTR IMPL BIP LD · Class 2 · Implant

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 00681490064583), received between Sep 26, 2019 and Sep 26, 2019 — classified as 1 malfunction.

The most frequently reported specific device problem is “Mechanical 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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Device problems

  • Mechanical Problem1

Patient problems

  • No Known Impact Or Consequence To Patient1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • MalfunctionSep 26, 2019Mechanical Problem; Mechanical Problem

    IT WAS REPORTED THAT THE LEFT VENTRICULAR (LV) LEAD EXHIBITED A FRACTURE. THE LV LEAD WAS CAPPED AND REPLACED. IT WAS NOTED THE SET SCREW OF THE Y ADAPTOR WAS STRIPPED AND THE LEADS HAD TO BE CUT TO REMOVE THE ADAPTOR. THE ADAPTOR WAS SUBSEQUENTLY REMOVED. NO PATIENT COMPLICATIONS HAVE BEEN REPORTED AS A RESULT OF THIS EVENT.

    Patient problems: No Known Impact Or Consequence To Patient

    MAUDE report 9122603 ↗

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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.