Reported Apr 8, 2026 · Ongoing
Medline kits containing Olympus biopsy valves: 1. BAL KIT, DYNDA2137B 2. ENDO KIT, DYKE1915
Medline Industries, LP
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Medline Industries, LP · 3 Lakes Dr · Northfield, IL · 60093-2753
Is this the product you have?
- Medline
- kits containing Olympus biopsy valves
1. BAL KITDYNDA2137B 2. ENDO KITDYKE1915
- Lot codes and dates
- 1. UDI-DI 10195327501259 (EA) 40195327501250 (CS) LOTS2. UDI-DI 10195327371029 (EA) 40195327371020 (CS) LOTS 24FBM018 24GBL319
24DBW06524EBV30124HBB49224JBW14325ABG41325CBH35925DBD21325GBP56925HBQ08825KBF72526ABE643
- 1. UDI-DI 10195327501259 (EA) 40195327501250 (CS) LOTS
- Amount recalled
- 14,379 kits total
This recall covers 10 products
The agency filed one notice per product. You are reading one of them; the other 9 are below.
Where it was sold
Why it was recalled
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.
This product could cause temporary or reversible health problems — stop using it.
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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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