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U.S. Department of Health and Human Services

Class 2 Device Recall IceRod "Cryoablation Needles

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 Class 2 Device Recall IceRod "Cryoablation Needlessee related information
Date Initiated by FirmNovember 18, 2020
Create DateDecember 22, 2020
Recall Status1 Completed
Recall NumberZ-0688-2021
Recall Event ID 86777
510(K)NumberK051052 
Product Classification Unit, cryosurgical, accessories - Product Code GEH
ProductIceRod" Prostate Cryoablation Kit
Code Information UPN: FPRPR3070  UDIs: 7290104830082, 7290104830082, 7290104830082, 7290104830082, 7290104830082, 7290104830082, 7290104830082, 7290104830082, 7290104830082, 7290104830082, 7290104830082, 7290104830082  Batch Numbers: U0412, U0029, U0039, T0775, T0687, T0675, A1873, A1866, A1820, A1643, A1420, A1226
Recalling Firm/
Manufacturer		 Boston Scientific Corporation
1 Scimed Pl
Maple Grove MN 55311-1565
For Additional Information ContactNicole Pshon
763-494-1700
Manufacturer Reason
for Recall		Complaint trend regarding needle shaft gas leaks.
FDA Determined
Cause 2		Under Investigation by firm
ActionCustomers will be sent a product advisory via overnight mail.
Quantity in Commerce64 units
DistributionNationwide
Total Product Life CycleTPLC Device Report
1 A record in this database is created when a firm initiates a correction or removal action. The record is updated if the FDA identifies a violation and classifies the action as a recall, and it is updated for a final time when the recall is terminated. Learn more about medical device recalls.
2 Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall.
510(K) Database510(K)s with Product Code = GEH
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