Medline Right Heart Cath Pack CTX Recall
Areazine synthesizes this FDA recall directly from FDA's official public data feed. See our methodology for full source attribution and refresh cadence.
Medline Industries is recalling 9,272 convenience kits containing Swan-Ganz catheters due to potential leaks and breakage that may cause infection or blood loss.
What this FDA recall tells you, and what most readers miss
This notice was issued by FDA on August 7, 2026 and geographically references United States. Its severity classification of "medium" signals how the issuing agency weighs the risk of harm if no action is taken - "critical" and "high" tier alerts typically carry direct consumer actions, while "medium" and "low" tend toward informational guidance or monitoring advisories. The category it belongs to - FDA Recalls - determines the consumer-protection framework behind it, which shapes what remedies (refunds, replacements, repairs, or the recall itself) are available to affected consumers and which agency holds statutory responsibility for enforcement.
Most readers skim a notice like this, check whether they are personally affected, and move on. The more useful lens is to verify its scope, source, and timestamp, then compare related notices without assuming that one record proves a broader trend.
Areazine pairs this record with the original agency URL so you can check the primary source before acting. Its related labels are recall, product-safety, fda, Devices.
What Happened
Medline Industries, LP is recalling convenience kits that contain Swan-Ganz catheters previously recalled by Becton Dickinson (BD). The catheters have a risk of leaks, lumen damage, or breakage at the blue proximal injectate lumen hub.
Which Products Are Affected
The affected product is the Medline Convenience kits containing recalled Swan-Ganz Catheters, specifically RIGHT HEART CATH PACK CTX DYNJ68530B. A total of 9,272 kits are involved under UDI-DI 10195327345044 with lots: 23DBI807, 23FBG708, 23GBK642, 23KBO477, 24BBG198, 24FBN889, 24GBJ879, 24HBR045, 24LBT492, 25ABL957, 25BBN572, 25GBT734, 25HBQ817, 25LBM617, 26BBK766, 26DBE720. Distribution was nationwide in AZ, CA, FL, IL, MO, NJ, OH, OK, TN, TX, and WI. Recall number Z-2606-2026.
What You Should Do
Consumers should stop using the affected kits and contact Medline Industries for return or refund instructions.
Why This Matters
The defect may lead to infection, medication loss, or blood loss.
Source
FDA Recall Z-2606-2026 - Medline Industries, LP
Original source: FDA Official Notice ↗
Related FDA Recalls
All FDA Recalls →Nationwide notices with similar length or severity timing 8
Two Areazine-derived peer sets for this FDA recall: nearest notices by body length and by same severity near the same agency date. Peers come from other categories so they are not the same-feed Related list above.
Similar body length
Nearest notices by article body length (1,075 characters here).
Similar severity timing
Same severity (medium) notices issued closest in time to August 7, 2026.
Frequently Asked Questions
Common questions about this FDA recall.