AutoPulse Resuscitation System Model 100 — Class II medical device recall Z-0658-2013
Terminated recall by Zoll Circulation, Inc., reported 2013-01-16. Complaints associated with an unexpected stop in AutoPulse compressions.
| Recall number | Z-0658-2013 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Zoll Circulation, Inc., Sunnyvale, CA, United States |
| Recall initiated | 2012-08-08 |
| Classified | 2013-01-09 |
| Reported by FDA | 2013-01-16 |
| Terminated | 2014-05-12 |
| Model numbers | 100 |
Product
AutoPulse Resuscitation System Model 100, Mfg by:Zoll Circulation Sunnyvale, CA. The AutoPulse Model 100 Automatic Mechanical Chest compressor is intended to be used as an adjunct to manual CPR, on adult patients only, in cases of clinical death as defined by lack of spontaneous breathing and pulse.
Reason for recall
Complaints associated with an unexpected stop in AutoPulse compressions.
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-0658-2013. 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.