- Recalling firm
- Medline Industries, LP
- 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 products (lot / model / serial)
- CDS982269K UDI-DI 10193489906844 Lots 21HBN691 21JBQ518 21LBD444 CDS982269L UDI-DI 10195327018016 Lots 21LBP501 22ABR514 22BBE936 22FBV989 CDS982269M UDI-DI 10195327192808 Lots 22JBE028 22LBF124 23ABP909 23CBO580 CDS982269N UDI-DI 10195327352998 Lots 23GBC969 23HBS959 23KBW067 23LBF510 24CBO691 24DBR250 24EBU619 24GBF288 25ABM339 25CBJ666 25HBH657 25IBM477 26BBG451 DYNJ901328D UDI-DI 10193489854923 Lots 21CBQ397 21FBJ935 21HBR220 21JBV897 21JBV898 22ABG611 DYNJ901328F UDI-DI 10195327044572 Lots 22CBX749 22FBX103 23ABC195 23EBG860 23EBL637 23EBS968 23FBM688 23GBS043 24EBL355 24FBJ301 24IBS567 24JBD767 24JBU518 24KBL806 24LBF815 25DBF590 25FBQ740 25GBH267 25JBQ634 DYNJ903465F UDI-DI 10193489918397 Lots 21FDB453 21HDB016 21IDB927 21KDA273 21LDA283 21LDB750 22CDA262 DYNJ903465G UDI-DI 10195327175559 Lots 22FDA593 22IDA677 22KDA077 23ADB246 DYNJ907857 UDI-DI 10193489909364 Lots 21GBJ159 21IBX945 21LBJ320 22ABH627 DYNJ907857A UDI-DI 10195327133160 Lots 22HBK592 22KBM436 DYNJ907857B UDI-DI 10195327256869 Lots 22KBN208 23ABM669 23IBE277 DYNJ905857A UDI-DI 10193489946680 Lots 22CBW896 22DBR508 22GBG113 22GBW887 22IBU528 22JBA758 22KBJ132 23ABP277 23ABP278 23ABS778 23DBD840 23EBJ932 23EBR134 23FBM591 23FBS624 23HBU190 24FBG082 24GBE581 24HBM636 24IBS825 24JBV903 24KBU708 24LBU110 25BBG391 25CBJ747 25DBP832 CDS981161AA UDI-DI 10193489303407 Lots 21DBH590 21DBU485 CDS981161AB UDI-DI 10193489817461 Lots 21DBT869 21FBD406 21FBK899 21HBT158 21IBJ277 21IBW875 22BBA363 22DBH285 22DBT988 22HBO231 22HBT037 22JBT785 DYNJ905437A UDI-DI 10193489571905 Lots 21ABH889 21DBE110 21EBH610 DYNJ909090 UDI-DI 10195327268350 Lot 23EBD437 DYNJ909090C UDI-DI 10198459084768 Lots 24HBR121 24KBT550 DYNJ9855016R UDI-DI 10193489481730 Lot 21DKA468 DYNJ9855016S UDI-DI 10193489904659 Lots 21HBC511 21HBC512 22GBZ353 22JBA413 22OBI292 22OBL745 23BBA924 23BBN806 23CBM193 CDS984289J UDI-DI 10193489263046 Lots 21BKA389 21DKA676 21FLA954 21GLA057 21GLA312 21GLB087 21HLA680 21ILA628 21KLB205 CDS983849D UDI-DI 10193489278231 Lots 21ABW164 21BBR951 21CBU594 21DBV510 21EBA170 21FBS444 21GBM142 21HBK335 21JBS153 21JBX783 21LBF083 22BBY971 22CBU521 22EBK057 22EBV010 22GBJ239 22GBZ470 22OBM677 CDS983849F UDI-DI 10195327228316 Lots 22JBN998 22KBB265 22LBT079 23ABN910 23ABO447 23DBG442 23EBP559 23FBP234 23FBV862 23GBN607 23HBA321 23IBM362 23JBQ839 24ABE486 24BBC426 CDS983849G UDI-DI 10195327650148 Lots 24EBA261 24FBD116 24GBH789 24HBQ756 24HBV600 24IBV160 24LBB436 25ABD357 25ABL507 25ABO737 25BBM406 25CBL909 25EBN768 25GBC295 25HBJ455 25JBJ254 25LBJ730 25LBQ452 26ABV988 26CBR016 26EBG732 DYNJ900377P UDI-DI 10193489818710 Lots 21ABS254 21DBG173 21EBM044 21FBJ060 21GBC753 DYNJ904311C UDI-DI 10193489427141 Lots 21CBD905 21DBT916 CDS983513F UDI-DI 10193489843729 Lots 21FBF442 21GBV619 21KBR342 22ABG599 22BBX671 22GBI891 22HBI664 22KBI289 23BBE439 CDS982523K UDI-DI 10193489372199 Lots 21AKB056 21CKA531 21DKA456 21EKA149 21FKA087 21GKA019 21HKA157 21HKA477 22ALA702 CDS982523L UDI-DI 10195327111151 Lots 22CLB415 22DLA940 22FLA279 22HLA254 22JLA168 22JLA569 22LLA984 23ALA240 23ALA433 23BLA324 23CLA025 23DLA469 23DLB096 23HLB221 23ILA547 23JLB156 CDS982523N UDI-DI 10198459094187 Lots 24JLA242 25ALA328 25BLA052 25CLA357 25ELB103 25GLA805 25HLA714 25JLA015 25JLA997 25LLA549 26ALA715 26BLA627 DYNJ908179 UDI-DI 10193489999082 Lot 21KBU602 DYNJ908179
- Units affected
- 9,272 kits
- Distribution pattern
- US Nationwide distribution in the states of AZ, CA, FL, IL, MO, NJ, OH, OK, TN, TX, WI.
- Firm location
- Northfield, IL, United States
- Recall type
- Voluntary: Firm initiated
- How the firm notified customers
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Product type
- Devices
- Status
- Ongoing
- Recall number
- Z-2613-2026
- Recall initiated
- May 28, 2026
- FDA classification date
- June 26, 2026
- FDA report date
- July 8, 2026
- FDA event ID
- 99209
- Last updated on HTM Vibe
- July 23, 2026