Boston Scientific recalls IceFORCE 2.1 CX Cryoablation Needles (UPN: FPRPR3604) due to unexpected electrolysis causing needle surface deterioration during procedures. Affected units include specific batch numbers listed in the recall notice.
The needle surface deteriorated due to unexpected electrolysis during procedure.
Boston Scientific is recalling IceFORCE 2.1 CX Cryoablation Needles because the needle surface can deteriorate during procedures due to unexpected electrolysis. This could lead to potential complications during surgical tissue destruction. Affected units have specific batch numbers listed in the recall notice.
The needle surface deteriorates due to unexpected electrolysis during surgical procedures. This could potentially cause issues with the needle's performance or safety during tissue destruction.
Medical professionals using the IceFORCE 2.1 CX Cryoablation Needles for surgical procedures are likely affected. Those with the specific batch numbers listed in the recall notice are at risk.
Check for the product name 'IceFORCE 2.1 CX Cryoablation Needle' and the specific batch numbers listed in the recall notice (e.g., A1564, A1521, A6723).
Identify the batch numbers listed in the recall notice (e.g., A1564, A1521, A6723) to confirm if your needle is affected.
The needle surface can deteriorate due to unexpected electrolysis during procedures, which may affect safety during surgical tissue destruction.
Affected batch numbers include A1564, A1521, A6723, A6908, A6929, A7015, T0025, T0056, T0137, T0138, T0269, U0041, A1203, A1549, A6734, A6916, A6928, A6931, A7083, T0156, T0166, U0042.
The recall notice does not specify a remedy, so no action is required beyond checking if your needle is affected.
We’ve drafted a message you can send Boston Scientific to request your refund or repair — edit it as you like.
Subject: Recall Z-2677-2020 — Boston Scientific Boston Scientific Hello, I own a Boston Scientific that is covered by recall Z-2677-2020 from Boston Scientific. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
