Boston Scientific recalls Preventive Maintenance Kit ICEFX (UPN SPRPM800: Batch 108159110) due to desiccant tube subassemblies with improperly tightened end caps. Affected users should contact the company for details.
Certain desiccant tube subassemblies were built with end caps that were not correctly tightened.
Boston Scientific is recalling Preventive Maintenance Kit ICEFX (UPN SPRPM8000, Batch 108159110) because some desiccant tube subassemblies have end caps that weren't tightened correctly. This could lead to the desiccant tube leaking, which might cause the kit to malfunction or fail during use.
The desiccant tube subassemblies have end caps that weren't tightened correctly. This can cause the desiccant tube to leak, potentially leading to the kit malfunctioning or failing during use. The risk is low because the leak is unlikely to cause serious injury.
Users of the Preventive Maintenance Kit ICEFX (UPN SPRPM8000, Batch 108159110) who purchased it from the manufacturer or authorized dealers. Medical device users are most at risk if the kit is used improperly.
Check for the Preventive Maintenance Kit ICEFX with Material Number (UPN) SPRPM8000 and Batch number 108159110. The product was sold by Boston Scientific Corporation.
Reach out to Boston Scientific Corporation for specific instructions on how to handle the recalled kit.
The recall is for a low-risk issue where desiccant tube subassemblies may have improperly tightened end caps, but it does not pose a serious injury risk.
Check for the Preventive Maintenance Kit ICEFX with Material Number (UPN) SPRPM8000 and Batch number 108159110.
Contact Boston Scientific Corporation for specific instructions on how to handle the recalled kit.
We’ve drafted a message you can send Boston Scientific to request your refund or repair — edit it as you like.
Subject: Recall Z-2551-2025 — Boston Scientific Boston Scientific Hello, I own a Boston Scientific that is covered by recall Z-2551-2025 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.
