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Boston Scientific Corporation recalls IceFORCE" 2.1 CX 90¿ Cryoablation Needle
Recalled December 30, 2020 · FDA recall Z-0657-2021 · Boston Scientific
Hazard
Complaint trend regarding needle shaft gas leaks. · FDA Class II
Units
22,289 units
Sold at
Nationwide
Description
Complaint trend regarding needle shaft gas leaks.
Product
IceFORCE" 2.1 CX 90¿ Cryoablation Needle
Manufacturer(s)
Boston Scientific Corporation
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →