Data Foundry

Medical device recalls 2014

Zoll Circulation LifeBand Single Pack — Class III medical device recall Z-2090-2014

Terminated recall by Zoll Circulation, Inc., reported 2014-07-30. Typographical error in the Japanese legal label of the AutoPulse Resuscitation System Model 100. The label is

Recall numberZ-2090-2014
Product typeMedical device
ClassificationClass III
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmZoll Circulation, Inc., San Jose, CA, United States
Recall initiated2013-07-16
Classified2014-07-22
Reported by FDA2014-07-30
Terminated2014-07-22
Countries outside the USJP
Reason classeslabeling
NDC08700-0702-03
Lot numbers41515
Serial numbers03690, 03695, 03696, 03700, 03701, 03702, 03706, 03707, 03708, 03709, 03710, 03711, 03715, 03717, 03718, 03720, 03721, 03726, 03727, 03728, 03730, 03732, 03733, 03734, 03736 and 136 more
Model numbers100

Product

Zoll Circulation LifeBand Single Pack (accessory), and Nickel-metal hydride (NIMH) Battery. The LifeBand is a chest compression assembly that consists of a cover plate and two bands integrated with a compression pad with a Velcro fastener. The AutoPulse Battery is a removable component that supplies power for the AutoPulse operation. Used in the AutoPulse Resuscitation System Model 100, for chest compressions as an adjunct to manual CPR.

Reason for recall

Typographical error in the Japanese legal label of the AutoPulse Resuscitation System Model 100. The label is specific to the Japanese version of the product.

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2090-2014. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.