Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO WRP (5PK), REF H74908526512; cardiac catheter — FDA record Z-1675-2024

Reported ongoing

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date Mar 21, 2024. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; check FSIS directly. Source coverage and dates.

What the record says

Product
Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO WRP (5PK), REF H74908526512; cardiac catheter
Reason
An increase in complaints related to an inability to advance the guidewire through the lumen of the device for certain batches. There is evidence of the polyurethane layer delaminating and in some instances material detachment in the catheters inner lining.
Classification
Class I
Recalling firm
Boston Scientific Corporation
Quantity
8575 catheters
Agency-reported status
Ongoing
Source record identifier
Z-1675-2024

Open the official record

What the recall classes mean. Classification is an agency assessment, not individual medical advice.

Lot and product identifiers

Label fieldDetails supplied by the agency
Lot, code or applicabilityUDI/DI 08714729249504, Batch Numbers: 60442603, 60448206, 60463966, 60481407, 60491911, 60492607, 60443053, 60457140, 60467045, 60485945, 60492554, 60492608, 60443054, 60457142, 60467046, 60488392, 60492605, 60448186, 60463965, 60481406, 60488393, 60492606

Match all identifying details in the current notice. A brand name alone is not enough.

Distribution

Worldwide distribution. US, US Territories, EMEA, Canada, LATAM and Asia Pacific countries/regions.

No US distribution state could be established from this record. Check the official notice.

Dates in the source

Report date
May 22, 2024
Recall initiation date
Mar 21, 2024
Center classification date
May 10, 2024

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

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