Data Foundry

Medical device recalls 2025

Reprocessed Webster CS Catheter 10 Electrodes for… — Class I medical device recall Z-2611-2025

Ongoing recall by Medline Industries, LP, reported 2025-10-08, distributed nationwide. Specific lots of reprocessed electrophysiology and ultrasound catheters may contain small residual particulate

Recall numberZ-2611-2025
Product typeMedical device
ClassificationClass I
StatusOngoing
Voluntary or mandatedVoluntary
Recalling firmMedline Industries, LP, Northfield, IL, United States
Recall initiated2025-07-31
Classified2025-09-26
Reported by FDA2025-10-08
DistributedNationwide (US)
Quantity7,913 eaches
Reason classesspecification failure
UPC / GTIN / UDI-DI10197344044023, 10197344044030, 10197344044047, 10197344044054
Lot numbersEP241216, EP241218, EP241226, EP241231, EP250110, EP250121, EP250210
Model numbersBD710DF282CRH, BD710DF282RRH, BD710FJ282CRH, BD710FJ282RRH

Product

Reprocessed Webster CS Catheter 10 Electrodes for electrophysiological mapping of cardiac structures. Medline Item Numbers BD710DF282CRH BD710DF282RRH BD710FJ282CRH BD710FJ282RRH

Reason for recall

Specific lots of reprocessed electrophysiology and ultrasound catheters may contain small residual particulates. If devices with residual particulates on patient-contacting surfaces are used, there is a potential risk of an inflammatory response or systemic infection, and if particulate were to dislodge during use and contact circulating blood and/or the heart, it may produce a granulomatous reaction or thrombus formation, which may lead to cerebral or pulmonary embolism, or deep vein thrombosis.

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2611-2025. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.