AutoPulse Li-ion Battery™ 100 (REF 8700-0752-02)Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00849111001854), received between Nov 29, 2017 and Jun 18, 2020 — classified as 2 malfunctions.

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. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.

Most reported problems

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• MalfunctionJun 18, 2020Battery Problem; Battery Problem

  DURING PATIENT USE, THE AUTOPULSE PLATFORM (SN: (B)(4)) STOPPED FUNCTIONING AND TURNED OFF AFTER PERFORMING A FEW COMPRESSIONS. IN ADDITION, THE CUSTOMER REPORTED THAT AUTOPULSE LI-ION BATTERY (SN: (B)(4)) WAS STUCK IN THE BATTERY COMPARTMENT OF THE AUTOPULSE PLATFORM. AS PER THE CUSTOMER, THERE WERE NO BREAKAGES OBSERVED ON EITHER THE BATTERY FINGER LATCH OR ON THE AUTOPULSE BATTERY COMPARTMENT. NO CONSEQUENCES OR IMPACT TO THE PATIENT. PLEASE SEE THE FOLLOWING RELATED MFR REPORT: MFR # 3010617000-2020-00622 FOR THE AUTOPULSE PLATFORM (SN: (B)(4)).

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 10172192 ↗
• MalfunctionNov 29, 2017Low Battery; Device Operates Differently Than Expected; Low Battery; Device Operates Differently Than Expected

  AS REPORTED, DURING SHIFT CHECK, THE LI-ION BATTERY (B)(4) WAS INDICATING FOUR GREEN LEDS WHEN THE STATUS BUTTON WAS PRESSED. WHEN THE BATTERY WAS INSERTED INTO THE AUTOPULSE PLATFORM, IT WAS DISPLAYING AN ERROR MESSAGE "REPLACE / RECHARGE BATTERY". AFTER THE BATTERY WAS INSERTED INTO THE MULTI-CHEMISTRY CHARGER (MCC), IT WAS INDICATING FAIL (RED) LED. BATTERY STATUS HOWEVER, STILL INDICATING FOUR GREEN LEDS. NO PATIENT INVOLVEMENT WAS REPORTED.

  Patient problems: No Patient Involvement

  MAUDE report 7069663 ↗

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