Boston Scientific Corporation recalls IceFORCE" 2.1 CX Cryoablation Needle
Recalled Product
IceFORCE" 2.1 CX Cryoablation Needle
Hazard / Issue
Complaint trend regarding needle shaft gas leaks.
Issued by
FDA
Distribution: Nationwide (United States)
Lot/Code Info: UPN: FPRPR3604 UDIs: 7290104831027, 7290104831027, 7290104831027, 7290104831027, 7290104831027, 7290104831027, 7290104831027, 7290104831027, 7290104831027, 7290104831027, 7290104831027, 7290104831027, 7290104831027, 7290104831027, 7290104831027 Batch Numbers: U0903, U0785, U0617, U0042, T0166, T0156, A7083, A6931, A6928, A6916, A6734, A1549, A1527, X1483, A1203
View official government recall
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