AutoPulse Li-ion Battery™ 100 (REF 8700-0752-04)Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00849111002660), received between Mar 24, 2020 and Mar 24, 2020 — classified as 1 malfunction.

The most frequently reported specific device problem is “Battery Problem” (1 report).

1 other recall cover devices cleared under the same FDA submission (K112998); they may or may not involve this specific model.

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

Recent adverse event reports

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

• MalfunctionMar 24, 2020Battery Problem; Battery Problem

  NO LED LIGHTS ILLUMINATED ON THE AUTOPULSE LI-ION BATTERY (SN: (B)(4)) WHEN THE BATTERY STATUS BUTTON WAS PRESSED. THE AUTOPULSE PLATFORM DOESN'T FUNCTION WHEN IT IS POWERED ON WITH THIS BATTERY. IT IS UNKNOWN WHEN THE REPORTED ISSUE OCCURRED. HOWEVER, THERE WAS NO REPORT OF PATIENT CONSEQUENCES, AND THE CUSTOMER DIDN'T PROVIDE ANY FURTHER INFORMATION.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 9876159 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K112998. One submission often covers many models, so check the product and lot details in each record.

• Z-0118-2023 · Sep 22, 2022 · Open, Classified
  AutoPulse Li-ion Battery used on the AutoPulse Resuscitation System Model 100. used as an adjunct to manual CPR