Boston Scientific Recalls Prostate Cryoablation Kits Due to Needle Surface Deterioration
Boston Scientific is recalling 71 IceFORCE 2.1 Prostate Cryoablation Kits because needle surfaces deteriorated due to unexpected electrolysis during procedures.
What this means for you
Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.
Our severity reasoning: The recall is classified as FDA Class II, and the source describes a physical defect (needle surface deterioration) in a surgical device without reporting specific injuries or illnesses, fitting the criteria for a high-risk product where injury has not yet been reported.
Plain-English summary
Boston Scientific Corporation is recalling 71 units of the Ablation Galil Technology, Three IceFORCE 2.1 Prostate Cryoablation Kit Visual ICE System. The recall involves specific Galil Medicals 2.1 CX Cryoablation Needles intended for cryoablative destruction of tissue during surgical procedures.
The recall was initiated because the needle surface deteriorated due to unexpected electrolysis during the procedure. The affected devices were distributed nationwide to 40 states and the District of Columbia, as well as to Canada.
Healthcare providers and patients should stop using the affected devices immediately. Boston Scientific is the recalling firm responsible for managing the recall. Specific batch numbers and product codes are listed in the official recall documentation.
The recalled product
- Product
- Ablation Galil Technology, Three IceFORCE 2.1 Prostate Cyroablation Kit Visual ICE System, Prescription Only Galil Medicals 2.1 CX Cryoablation Needles are intended for cryoablative destruction of tissue during surgical procedures.
- Manufacturer
- Boston Scientific Corporation
- Affected units
- 71
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (20)
- UPN:FPRPR3608
- GTIN: 7290104831065
- Batch: A1170
- A1583
- A1937
- A6710
- A6744
- A6857
- A6900
- A6913
- A6926
- A7014
- A7027
- A7122
- T0055
- T0144
- T0181
- T0211
- T0212
- T0238
Distribution
Part of a larger recall action
This product is one of 10 recalled by Boston Scientific Corporation under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
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