Data Foundry

Medical device recalls 2025

GE Healthcare Optima XR240amx — Class II medical device recall Z-0813-2025

Ongoing recall by GE Medical Systems, LLC, reported 2025-01-15. GE HealthCare has become aware that in certain Optima XR200/220/240amx systems that have had a column replacem

Recall numberZ-0813-2025
Product typeMedical device
ClassificationClass II
StatusOngoing
Voluntary or mandatedVoluntary
Recalling firmGE Medical Systems, LLC, Waukesha, WI, United States
Recall initiated2024-11-25
Classified2025-01-07
Reported by FDA2025-01-15
Quantity120 units
UPC / GTIN / UDI-DI00840682122351
Serial numbers00130MOB16, 00158MOB17, 082407100689, 082407250223, 206223OPTIMA1, 206248OPT2, 206341OPT2402, 210METM2, 212838OPTIMA1, 219326AMX2, 228867XR240, 228867XR240C, 252847PP241, 256543OPT, 256543OPT1, 256HHPORT5, 256HHPORT6, 260824XR240, 270793OPT, 270793OPT1, 281274OPT1, 281338CL240, 281VHVXR240, 304256OPTIMA240, 305682DIG1 and 94 more

Product

GE Healthcare Optima XR240amx, Mobile Digital Radiographic System, Model Numbers: 1) 5555000-27; 2) 5555000-31; 3) 5555000-33; 4) 5555000-41; 5) 5555000-47; 6) A0700DL; 7) A1700DA; 8) To be provided.

Reason for recall

GE HealthCare has become aware that in certain Optima XR200/220/240amx systems that have had a column replacement performed, some bolts used in the Column Safety mechanism can be missing. If these bolts are missing and a failure of the internal counterpoise cable occurs, the Column Safety mechanism will not work properly causing the arm with X-ray tube and collimator to drop downward on the column track.

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-0813-2025. 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.