Data Foundry

Medical device recalls 2022

GE Vscan Extend — Class II medical device recall Z-0522-2022

Terminated recall by GE Healthcare, LLC, reported 2022-02-02, distributed in AK, AL, AR, AZ, CA, CO, CT, DC…. The firm identified that the Vscan Extend device will not power on because of depleted battery, due to the dev

Recall numberZ-0522-2022
Product typeMedical device
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmGE Healthcare, LLC, Waukesha, WI, United States
Recall initiated2021-11-04
Classified2022-01-24
Reported by FDA2022-02-02
Terminated2026-07-24
DistributedAK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, PR, RI, SC, SD, TN, TX, UT, VA, WA, WI, WV, WY
Countries outside the USAE, AT, AU, BD, BE, BG, BH, BR, CA, CH, CL, CN, CO, CY, CZ, DE, DK, EC, EE, ES, FI, FR, GB, GR, HR, HT, HU, ID, IE, IL, IN, IR, IS, IT, JP, KR, KW, LB, LT, MA, MT, MX, MY, NL, NO, NZ, PH, PL, PT, QA, RO, RS, RU, SA, SE, SG, SI, SK, SV, TH, TR, TT, UA, VN, ZA
Model numbers8090021VH150268HX, H41212Z, VH150155WU, VH150156AL, VH1501577F, VH150158WG, VH150159BV, VH150160GN, VH150161AV, VH150162V8, VH150163A7, VH1501645D, VH150165PH, VH150166K3, VH1501674A, VH150168SL, VH150169JA, VH150170FS, VH150171DB, VH150172HJ, VH1501731X, VH150174CH, VH1501756Y, VH150176XW, VH150177RI and 475 more

Product

GE Vscan Extend, being sold as "Vscan Extend Sector DICOM"

Reason for recall

The firm identified that the Vscan Extend device will not power on because of depleted battery, due to the device not being turned off prior to battery removal or when being connected to a computer without AC power.

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-0522-2022. 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.