THORACIC ROBOTS, DYNJ908777B Recall
Issued April 8, 2026 · Medline Industries, LP
In April 2026, Medline Industries, LP recalled the THORACIC ROBOTS, DYNJ908777B, a serious health recall reported by the FDA. Affected owners are eligible for a voluntary. Here is what the hazard is and exactly what to do about it.
Compiled by Maya Ellison, RecallCheckr
What this means for you
Kits contain recalled Olympus biopsy valves. Olympus is investigating an increase in complaints associated with rubber fragment detachment in the slit of single use biopsy valves. Potential consequences associated with detachment of fragments from valve include foreign body in patient's tracheobronchial tree, which may require intervention for removal. Other potential consequences include inflammatory response, hypoxia, and prolongation of procedure.
What you should do
- 1 Stop using THORACIC ROBOTS, DYNJ908777B right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact Medline Industries, LP to arrange your voluntary. See the official notice below for contact details.
- 4 Keep the product until your remedy is fully processed. You may need it.
Recall details
- Brand
- Medline Industries, LP
- Category
- Health
- Recall date
- April 8, 2026
- Units affected
- Not reported
- Sold at
- US Nationwide distribution in the states of CA, FL, IL, IN, KY, MA, MD, MT, NY, OH, PA, TN, TX.
- Recall number
- FDA-Z-1707-2026
- Made in
- United States
- Issuing agency
- FDA
In context
- Medline Industries, LP has 50 recalls in our database, including 8 rated Critical.
- We're tracking 3,576 Health recalls in our database.
- This is the 356th Health recall we've logged in 2026.