Z-2612-2025Class I

Reprocessed Inquiry Steerable Diagnostics Catheter for electrogram recording and cardiac stimulation during...

Name: Z-2612-2025 Reprocessed Inquiry Steerable Diagnostics Catheter for electrogram recording and cardiac stimulation during...
Creator: Medline Industries, LP
Published: 2025-07-31
License: https://open.fda.gov/license/

MEDLINE INDUSTRIES, LP - Northfield / initiated 2025-07-31 / Open, Classified

FDA source

Medline Industries, LP began a recall of Reprocessed Inquiry Steerable Diagnostics Catheter for electrogram recording and cardiac stimulation during diagnostic electrophysiologic studies; Medline Item... on 2025-07-31. FDA classified it as Class I and gives the reason as "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...". As of 2026-09-10, the recall status on record is Open, Classified.

Recall record

Recall number: Z-2612-2025
Classification: Class I
Status: Open, Classified
Initiated: 2025-07-31
Posted: 2025-09-26
Recalling firm: MEDLINE INDUSTRIES, LP - Northfield
Product: Reprocessed Inquiry Steerable Diagnostics Catheter for electrogram recording and cardiac stimulation during diagnostic electrophysiologic studies; Medline Item Numbers 81102RH 81104RH 81107RH 81174RH 81402RH 81404RH 81405RH 81472RH 81473RH 81474RH 81531RH 81532RH
Product code: NLH Catheter, Recording, Electrode, Reprocessed
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 root cause: Under Investigation by firm
Action: 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.
Quantity in commerce: 7913 eaches
Distribution: Domestic US distribution nationwide. International distribution pending. No international distribution.
Product codes and lots: Item Number/UDI-DI 81102RH 10197344133239; 81104RH 10197344133246; 81107RH 10197344133260; 81174RH 10197344133291; 81402RH 10197344133352; 81404RH 10197344133376; 81405RH 10197344133383; 81472RH 10197344133413; 81473RH 10197344133420; 81474RH 10197344133437; 81531RH 10197344133512; 81532RH 10197344133529; LOTS EP250212 EP250214

Enforcement reports

One row per recalled product line

FDA enforcement reports joined to recall event Z-2612-2025
Recall number	Class	Status	Voluntary or mandated	Report date	Classified
Z-2610-2025	Class I	Ongoing	Voluntary: Firm initiated	2025-10-08	2025-09-26
Z-2611-2025	Class I	Ongoing	Voluntary: Firm initiated	2025-10-08	2025-09-26
Z-2612-2025	Class I	Ongoing	Voluntary: Firm initiated	2025-10-08	2025-09-26
Z-2613-2025	Class I	Ongoing	Voluntary: Firm initiated	2025-10-08	2025-09-26
Z-2614-2025	Class I	Ongoing	Voluntary: Firm initiated	2025-10-08	2025-09-26

Product code NLH

K242225Class IIMedline ReNewal Reprocessed Abbott Inquiry Steerable Diagnostic CatheterSurgical Instrument Service and Savings, Inc. / cleared 2024-11-29

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device recall database and the FDA enforcement reports, both ingested from openFDA. The recall record supplies the product, the reason and the product code; the enforcement report supplies the classification. The two datasets are exported by FDA on different days, and the date above is the older of the two, so nothing on this page is newer than it says.

MDM adds the root cause tag, derived from FDA’s own root cause text, and the cross-links to the product code, the clearances named on the record and MDM coverage. Where a recall has not been joined to an enforcement report, no classification is shown.

Data as of 2026-09-30, the FDA export date for this dataset. Page last changed 2026-09-05. View this recall on fda.gov (opens on fda.gov)