FDA Device recall Z-0521-2022
GE Vscan Extend, being sold as "Vscan Extend Dual Wi-Fi"
- FDA Device
- Class II
- terminated
- Published 2022-02-02
On 2022-02-02 the FDA classified a Class II recall of GE Vscan Extend, being sold as "Vscan Extend Dual Wi-Fi" by Ge Healthcare, citing 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 conne….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0521-2022 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2021-11-04 |
| Published | 2022-02-02 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Ge Healthcare |
| Distribution | AK, 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 |
Product
GE Vscan Extend, being sold as "Vscan Extend Dual Wi-Fi"
Reason
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.
Identifiers
| code_info | Information reads "Serial Number (UDI, Model Number)". VH161002TY (01008406821216511117092521VH161002TY, H41212RL), VH…Information reads "Serial Number (UDI, Model Number)". VH161002TY (01008406821216511117092521VH161002TY, H41212RL), VH161494JD (01008406821216511118011021VH161494JD, H41212RL), VH161911LV (01008406821216511118030021VH161911LV, H41212RL), VH163440GG (01008406821216511118121421VH163440GG, H41212YZ), VH261421ZS (01008406821216511120040021VH261421ZS, H41212YZ), VH162444U2 (01008406821216511118060021VH162444U2, H41212YZ), VH165272MV (01008406821216511119070021VH165272MV, H41212YZ), VH264483KQ (01008406821216511121011921VH264483KQ, H41212YZ), VH261426TR (01008406821216511120040021VH261426TR, H41212YZ), VH260601DD (01008406821216511120030021VH260601DD, H41212YZ), VH260693VL (01008406821216511120030021VH260693VL, H41212YZ), VH261300BX (01008406821216511120030021VH261300BX, H41212YZ), VH262303C1 (01008406821216511120061021VH262303C1, H41212YZ), VH1650459M (01008406821216511119060021VH1650459M, H41212YZ), VH26015148 (01008406821216511119120021VH26015148, H41212YZ), VH260359ZY (01008406821216511 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0521-2022%22
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