Recall of THORACIC ROBOTS DYNJ908777B by Medline Industries
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Medline Industries is recalling 14,379 kits of THORACIC ROBOTS DYNJ908777B due to issues with recalled components that could lead to health risks.
What this FDA recall tells you, and what most readers miss
This notice was issued by FDA on April 14, 2026 and geographically references United States. Its severity classification of "high" 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.
Recall Article
What Happened
Medline Industries, LP is recalling THORACIC ROBOTS DYNJ908777B kits because they contain recalled Olympus biopsy valves with complaints of rubber fragment detachment, which may result in a foreign body in the patient's tracheobronchial tree requiring intervention, along with potential inflammatory response, hypoxia, and prolonged procedures.
Which Products Are Affected
The affected products are THORACIC ROBOTS, DYNJ908777B. The recall involves 14,379 kits total, distributed nationwide in the United States, specifically in the states of CA, FL, IL, IN, KY, MA, MD, MT, NY, OH, PA, TN, and TX. The recall number is Z-1707-2026, and the codes include UDI-DI 10198459269196 (EA), 40198459269197 (CS), and lots: 25EBD732, 25GBG733, 25IBQ613, 25JBD457, 25KBT352, 26ABA235, 26ABP735.
What You Should Do
Consumers should stop using the affected products and contact the recalling firm, Medline Industries, LP, for instructions on returns or refunds, as this is a voluntary firm-initiated recall.
Why This Matters
This recall highlights potential health risks from medical devices, affecting thousands of kits and requiring intervention for patient safety in the United States.
Source
Attributed to the FDA. Recall number: Z-1707-2026.
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 (1,284 characters here).
Similar severity timing
Same severity (high) notices issued closest in time to April 14, 2026.
Frequently Asked Questions
Common questions about this FDA recall.