LifeBand® Load-distributing Band 100 (REF 8700-0701-02)Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00849111001595), received between Mar 29, 2019 and Mar 29, 2019 — classified as 1 malfunction.

The most frequently reported specific device problem is “Mechanical Jam” (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 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

• MalfunctionMar 29, 2019Retraction Problem; Mechanical Jam; Retraction Problem; Mechanical Jam

  DURING PATIENT USE, THE CUSTOMER REPORTED THE LIFEBAND WAS DETACHED AFTER PERFORMING COMPRESSIONS FOR A DURATION OF 35 MINUTES. NO ADDITIONAL INFORMATION WAS PROVIDED. NO CONSEQUENCES OR IMPACT TO PATIENT WAS REPORTED.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 8465491 ↗

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