FDA recall record

Boston Scientific Preventive Maintenance (PM) Kit ICEFX, Material Number (UPN) SPRPM8000 recall — FDA Z-2551-2025

Certain desiccant tube subassemblies were built with end caps that were not correctly tightened.

Class IIclassification
Z-2551-2025official record ID
Sep 17, 2025report date

Recall record at a glance

Official recordZ-2551-2025
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmBoston Scientific Corporation
Report dateSep 17, 2025
Recall initiation dateAug 18, 2025
Quantity1 unit
LocationMaple Grove, MN, United States

Official product description

Preventive Maintenance (PM) Kit ICEFX, Material Number (UPN) SPRPM8000

Why the product was recalled

Certain desiccant tube subassemblies were built with end caps that were not correctly tightened.

Distribution information

Worldwide - US Nationwide and the countries of Canada, France, Germany and Italy. (Preventive Maintenance Kit distributed to Canada only.)

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

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