The LIFEPAK 1000 defibrillator is intended for use by personnel who… — Class I medical device recall Z-1257-2017
Terminated recall by Physio-Control, Inc., reported 2017-03-15, distributed nationwide. The firm has received complaints that the LIFEPAK 1000 Defibrillator is unexpectedly powering off during devic
| Recall number | Z-1257-2017 |
|---|---|
| Product type | Medical device |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Physio-Control, Inc., Redmond, WA, United States |
| Recall initiated | 2017-01-13 |
| Classified | 2017-03-03 |
| Reported by FDA | 2017-03-15 |
| Terminated | 2019-08-22 |
| Distributed | Nationwide (US) |
| Countries outside the US | BH, BZ, CL, CN, DE, EC, HK, HN, ID, IN, JM, LK, NL, PH, SA, SG, TH, TN, UA |
| Model numbers | 320371500XX |
Product
The LIFEPAK 1000 defibrillator is intended for use by personnel who are authorized by a physician/medical director and are trained in CPR and the use of the LIFEPAK 1000 defibrillator.
Reason for recall
The firm has received complaints that the LIFEPAK 1000 Defibrillator is unexpectedly powering off during device usage.
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-1257-2017. 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.