Medline Industries, LP recalls Medline Convenience kits containing recalled Swan-Ganz Catheters CABG A CDS CDS98…
Reason for recall
Kits contain Swan-Ganz catheters recalled by Becton Dickinson (BD). BD has received complaints of leaks/breakage involving failures of the (blue) proximal injectate lumen hub on these catheters. This has led to instances of leakage, lumen damage, and breakage, and may lead to infection, medication loss, and/or blood loss.
Affected product
Check your device
Enter a lot, serial, REF, or UDI number from your device's label to check it against this recall's listed codes.
Affected products & lots
- Medline Convenience kits containing recalled Swan-Ganz Catheters CABG A CDS CDS982269K CDS982269L CDS982269M CDS982269N CARDIAC MAJOR DYNJ901328D DYNJ901328F HEART A DYNJ903465F DYNJ903465G HEART TRAY-VASCULAR DYNJ907857 DYNJ907857A DYNJ907857B KIT UNIVERSITY CABG PK DYNJ905857A OPEN HEART CDS981161AA CDS981161AB DYNJ905437A DYNJ909090 DYNJ909090C DYNJ9855016R DYNJ9855016S OPEN HEART ACCESSORY CDS CDS984289J OPEN HEART ANESTHESIA PACK CDS983849D CDS983849F CDS983849G OPEN HEART B CDS DYNJ900377P OPEN HEART BASIC B DYNJ904311C OPEN HEART CDS CDS983513F OPEN HEART CDS QVH CDS982523K CDS982523L CDS982523N OPEN HEART LINE SET UP DYNJ908179 DYNJ908179A OPEN HEART SUPPLEMENT DYNJ909116 DYNJ909116A DYNJ909116C DYNJ909116D SILVER CROSS OPEN HEART DYNJ906102J DYNJ906102K DYNJ906102L SM OPEN HEART PACK A&B DYNJ904749G DYNJ904749J VPH OPEN HEART DYNJ902664J DYNJ902664KDYNJ902664LUDI-DI 10193489906844398 affected lots21HBN69121JBQ51821LBD444CDS982269L1019532701801621LBP50122ABR51422BBE936
+390 more
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
What the firm is doing
On May 28, 2026, the firm notified customers via letters titled "URGENT MEDICAL DEVICE CORRECTION." Customers were referred to BD's recall notice, which provides advice for users and instructions to mitigate hub breakage issues. Product return is not required. If you have any questions, contact the Recall Department at 866-359-1704 or recalls@medline.com.
DistributionShow detailsHide
US Nationwide distribution in the states of AZ, CA, FL, IL, MO, NJ, OH, OK, TN, TX, WI.
Use of the product may cause temporary or medically reversible adverse health consequences.
Sources & references
- FDA enforcement recordOfficial FDA database entry for Z-2613-2026
- FDA device classification · OEZOfficial FDA classification for this device type
- CFR regulation · 21 CFR 870.1200The federal regulation governing this device
- FDA recall announcementSearch FDA.gov for the official press announcement
- Find Medline Industries, LPSearch for the manufacturer's official notice
- News coverageRecent reporting on this recall and manufacturer
- openFDA data recordThe raw JSON record this page is built from
Source: U.S. FDA openFDA device enforcement reports. This summary is informational and may lag or differ from the official record. Always verify against the FDA before acting.
Taylor Coteus is RecallWatch's Legal News Analyst, covering FDA medical-device enforcement and patient-safety litigation. He reviews every recall against the FDA's official openFDA record before it is published and is responsible for corrections and editorial accuracy.
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