Lightspeed 16 CT — Class II medical device recall Z-2801-2015
Terminated recall by GE Healthcare, reported 2015-09-30, distributed nationwide. Potential for expulsion of the Power Supply on Lightspeed CT scanner or Discovery ST PET CT or Discovery LS PE
| Recall number | Z-2801-2015 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | GE Healthcare, Waukesha, WI, United States |
| Recall initiated | 2015-07-17 |
| Classified | 2015-09-21 |
| Reported by FDA | 2015-09-30 |
| Terminated | 2016-03-08 |
| Distributed | Nationwide (US) |
| Countries outside the US | AR, AT, AU, BE, CA, CH, CN, DE, DK, EE, ES, FI, FR, GB, ID, IL, IN, IT, JP, KR, MX, NO, PL, SA, SE, SG, SK, TW, ZA |
| Quantity | 416 |
Product
Lightspeed 16 CT
Reason for recall
Potential for expulsion of the Power Supply on Lightspeed CT scanner or Discovery ST PET CT or Discovery LS PET CT scanner.
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-2801-2015. 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.