B. Braun SESK UPMC Double Catheter Tray Recall
Areazine synthesizes this FDA recall directly from FDA's official public data feed. See our methodology for full source attribution and refresh cadence.
B. Braun Medical Inc. is recalling 390 units of the SESK UPMC Double Catheter Tray due to a supplier issue with included MASTISOL Liquid Adhesive that may render the product unusable.
What this FDA recall tells you, and what most readers miss
This notice was issued by FDA on July 11, 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
B. Braun Medical Inc. initiated a voluntary recall after being notified by supplier Ferndale Laboratories, Inc. that MASTISOL Liquid Adhesive included in the trays may have cracking of the butyrate tubing, rendering the product unusable.
Which Products Are Affected
The recall covers SESK UPMC DOUBLE CATHETER TRAY, Model/Catalog Number 530134. Affected lot: 0062019148 (UDI-DI Primary Device 04046964305856, UDI-DI Unit Device ID 04046964305849). A total of 390 units were distributed nationwide in the states of AL, FL, PA, TX, VA, and WA. Recall number Z-2270-2026. Classification: Class II.
What You Should Do
Consumers should check for the affected lot number and contact B. Braun Medical Inc. for return or refund instructions.
Why This Matters
The recall affects a medical device distributed across multiple U.S. states and may impact product usability.
Source
FDA recall Z-2270-2026, B Braun Medical Inc., Bethlehem, PA.
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 (961 characters here).
Similar severity timing
Same severity (medium) notices issued closest in time to July 11, 2026.
Frequently Asked Questions
Common questions about this FDA recall.