Recall Z-2611-2025

Medline Industries, LP · initiated July 31, 2025

Class I Open, Classified

Class I – dangerous or defective products that could cause serious health problems or death

Product

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

Codes / lots: Item Number/UDI-DI BD710DF282CRH 10197344044023; BD710DF282RRH 10197344044030; BD710FJ282CRH 10197344044047; BD710FJ282RRH 10197344044054; LOTS EP241216 EP241218 EP241226 EP241231 EP250110 EP250121 EP250210

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.

FDA-determined cause: Under Investigation by firm

Action taken

On July 31, 2025, the firm notified customers via first class mail and email of the potential product issue. An updated letter was sent to customers on 8/13/25 with additional item and lot numbers. Affected products are to be returned for credit. Customers were instructed to immediately identify and quarantine all affected product within their possession. Once they have completed and returned the response form listing their affected inventory, they will receive return labels and RGA information. Customers will receive credit when the returned product is received.

Details

Recall number
Z-2611-2025
Initiated
July 31, 2025
Posted by FDA
September 26, 2025
Product code
NLH – Catheter, Recording, Electrode, Reprocessed
Quantity
7913 eaches
Distribution
Domestic US distribution nationwide. International distribution pending. No international distribution.
Recalling firm
Medline Industries, LP, Northfield, IL

Official FDA recall record

Other products in the same recall event

RecallProductInitiated
Z-2610-2025 Class IReprocessed Livewire Steerable Electrophysiology Catheter Item Numbers 401575RH 401582RH…Specific lots of reprocessed electrophysiology and ultrasound catheters may contain small residual… 07/31/2025Open, Classified
Z-2612-2025 Class IReprocessed Inquiry Steerable Diagnostics Catheter for electrogram recording and cardiac…Specific lots of reprocessed electrophysiology and ultrasound catheters may contain small residual… 07/31/2025Open, Classified
Z-2613-2025 Class IReprocessed ViewFlex Xtra ICE Catheter to visualize cardiac structures; blood flow and…Specific lots of reprocessed electrophysiology and ultrasound catheters may contain small residual… 07/31/2025Open, Classified
Z-2614-2025 Class IReprocessed ACUSON AcuNav Ultrasound Catheter for intracardiac and intra-luminal…Specific lots of reprocessed electrophysiology and ultrasound catheters may contain small residual… 07/31/2025Open, Classified