B. Braun CESK SHANDS JACKSONVILLE 20055717 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 680 units of CESK SHANDS JACKSONVILLE 20055717 devices due to a supplier recall of the MASTISOL Liquid Adhesive component.
What this FDA recall tells you, and what most readers miss
This notice was issued by FDA on July 10, 2026 and geographically references AL, FL, PA, TX, VA, WA. 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 was notified by supplier Ferndale Laboratories, Inc. that they issued a voluntary recall of MASTISOL Liquid Adhesive due to potential cracking of the butyrate tubing, which renders the product unusable.
Which Products Are Affected
Brand Name: B. BRAUN MEDICAL INC. Product Name: CESK SHANDS JACKSONVILLE 20055717 Model/Catalog Number: 555884 Lot Number: 0062036271 UDI-DI (Primary Device): 04046964317361 UDI-DI (Unit Device ID): 04046964317347 Product Quantity: 680 units Distribution: US Nationwide in the states of AL, FL, PA, TX, VA, WA Recall Number: Z-2269-2026 Classification: Class II
What You Should Do
The recall is ongoing. Affected products should not be used as they are rendered unusable.
Why This Matters
The recall involves 680 devices distributed across multiple states due to a component defect affecting product usability.
Source
FDA Event ID 98862, Recall Number Z-2269-2026 (https://www.fda.gov)
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 (958 characters here).
Similar severity timing
Same severity (medium) notices issued closest in time to July 10, 2026.
Frequently Asked Questions
Common questions about this FDA recall.