LIFEPAK 1000 defibrillator — Class II medical device recall Z-1660-2014
Terminated recall by Physio-Control, Inc., reported 2014-06-04, distributed nationwide. Physio-Control has become aware of incidents where customers have attempted to use their LIFEPAK 1000 defibril
| Recall number | Z-1660-2014 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Physio-Control, Inc., Redmond, WA, United States |
| Recall initiated | 2014-05-09 |
| Classified | 2014-05-23 |
| Reported by FDA | 2014-06-04 |
| Terminated | 2018-05-29 |
| Distributed | Nationwide (US) |
| Countries outside the US | AE, AR, AT, AU, BB, BD, BE, BH, BO, BR, CA, CH, CL, CN, CO, CR, CW, CY, CZ, DE, DK, EC, EG, ES, FI, FR, GB, GR, GT, HK, HR, HU, ID, IE, IL, IN, IQ, IR, IS, IT, JO, JP, KE, KR, KW, KY, LB, LK, LT, LV, MA, MT, MX, MY, NL, NO, NZ, OM, PA, PE, PH, PK, PL, PT, QA, RO, RS, RU, SA, SE, SG, SI, SK, TH, TN, TR, TW, UA, UY, VE, ZA |
| Reason classes | device malfunction, software |
| Serial numbers | 1297232, 32894157, 32895126, 32895130, 32895136, 32895306, 32895317, 32895437, 33468929, 34587902, 34587903, 34587904, 34587905, 34587906, 34587908, 34587909, 34587910, 34587911, 34587912, 34587913, 34587914, 34587915, 34587916, 34587917, 34587918 and 81 more |
| Model numbers | 320371500XXX, LP1000 |
Product
LIFEPAK 1000 defibrillator. Affected Part Numbers: 320371500XXX The LP1000 (in AED mode) is indicated for use on patients in cardiac arrest.
Reason for recall
Physio-Control has become aware of incidents where customers have attempted to use their LIFEPAK 1000 defibrillator and the device has shut down unexpectedly due to a very low battery. A defibrillator in this scenario has the potential to fail to deliver a shock, with the potential result that therapy is not delivered and a patient is not resuscitated. A software malfunction in the LIFEPAK 100
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-1660-2014. 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.