B. Braun CESK Riverside Health System 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 690 units of CESK Riverside Health System (Model 552126) due to a supplier issue with MASTISOL Liquid Adhesive tubing.
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 was notified by supplier Ferndale Laboratories, Inc. of 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: B. BRAUN MEDICAL INC.
- Product Name: CESK RIVERSIDE HEALTH SYSTEM
- Model/Catalog Number: 552126
- Lot Number: 0062031274
- UDI-DI (Primary): 04046955056903
- UDI-DI (Unit): 04046955056897
- Quantity: 690 units
- Distribution: US Nationwide in AL, FL, PA, TX, VA, WA
- Recall Number: Z-2268-2026
- Classification: Class II
- Status: Ongoing
What You Should Do
Consumers should follow instructions provided in the firm's notification letter.
Why This Matters
The recall affects 690 devices distributed across multiple states due to a component defect that makes the product unusable.
Source
FDA recall Z-2268-2026, 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 (919 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.