Medline kits containing Olympus biopsy valves recallZ-1709-2026 · Medline Industries, LP · initiated Feb 16, 2026
Open, Classified
Is my device affected?
- Compare the model, catalog and lot or serial numbers on your device or its packaging with the code information below. A recall usually covers only specific models or lots.
- If yours is listed, follow the instructions from Medline Industries, LP or your healthcare provider. The company's action is summarized under what the company is doing.
- Do not stop using a prescribed or implanted device on your own — talk to your healthcare provider first.
Where to find your model and lot numbers · What recall classes and statuses mean
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.
FDA root cause category: Under Investigation by firm
What the company is doing
Firm notified customers on 2/16/26. Consignees were provided with a copy of Olympus's notification, which includes reminders to follow the IFU. According to the firm, the component can continue to be utilized by the customer, along with the remainder of the kit.
Recall details
- Recall number
- Z-1709-2026
- Status
- Open, Classified
- Initiated by the company
- Feb 16, 2026
- Posted by the FDA
- Apr 1, 2026
- Recalling firm
- Medline Industries, LP
- Quantity
- 14,379 kits total
- Product code
- OGR
- Distribution
- US Nationwide distribution in the states of CA, FL, IL, IN, KY, MA, MD, MT, NY, OH, PA, TN, TX.
Product description
Medline kits containing Olympus biopsy valves: 1. BRONCHOSCOPY, DYNJ900898I DYNJ901922G 2. FLEXIBLE BRONCHOSCOPY KIT, DYKM1417I DYKM1417J 3. LARYNGOSCOPY/BRONCHOSCOPY PACK, DYNJ58146A 4. RIGID KIT, DYNDA2138A
Code information (models, lots, serial numbers)
Show the full code information (1k characters)
1. DYNJ900898I UDI-DI 10198459273513 (EA) 40198459273514 (CS) LOTS 25DME064 25HMD841 25JMD489 25KME329 25KMH848 25LMC029 25LMH235 25LMK305 DYNJ901922G UDI-DI 10195327640422 (EA) 40195327640423 (CS) LOTS 24KBP812 2. DYKM1417I UDI-DI 10195327456757 (EA) 40195327456758 (CS) LOTS 24DLA405 24ELA912 24GLA871 24ILA151 24JLA326 DYKM1417J UDI-DI 10198459191640 (EA) 40198459191641 (CS) LOTS 25BLA761 25BLA886 25DLA353 25ELA056 25FLA429 25HLA196 25HLA242 25KLA388 25KLA610 3. DYNJ58146A UDI-DI 10193489611977 (EA) 40193489611978 (CS) LOTS 23KDA851 24ADC096 24CDB107 24DDB887 24IDA855 24JDB494 24LDA691 25BMF825 25DMD969 25FMC760 25GMD422 4. DYNDA2138A UDI-DI 10193489874594 (EA) 40193489874595 (CS) 24DBM325 24DBM383 25DBK159
Devices named in this recall
6 devices in the FDA device registry whose identifier appears in the recall's code information.
- Medline Industries, Inc. DYNJ58146AMedline Industries, Inc. · Ear, nose, and throat surgical tray1 recall0 reports
- Medline Industries, Inc. DYNDA2138AMedline Industries, Inc. · Ear, nose, and throat surgical tray1 recall0 reports
- Medline Industries, Inc. DYKM1417IMedline Industries, Inc. · Ear, nose, and throat surgical tray1 recall0 reports
- Medline Industries, Inc. DYNJ901922GMedline Industries, Inc. · Ear, nose, and throat surgical tray1 recall0 reports
- Medline Industries, Inc. DYKM1417JMedline Industries, Inc. · Ear, nose, and throat surgical tray1 recall0 reports
- Medline Industries, Inc. DYNJ900898IMedline Industries, Inc. · Ear, nose, and throat surgical tray1 recall0 reports
Other products in the same recall event
The FDA groups related products into one recall event (event 98530).
- Z-1705-2026 · Open, ClassifiedAirway Exam Kit, DYKE1796
- Z-1706-2026 · Open, ClassifiedMedline convenience kits containing Olympus biopsy valves: 1. BRONCH PACK, DYKE2096 2. NON MB BRONCHOPSCOPY CCH LH PK, DYNJT6182 3. PULMONARY BRONCH PACK, DYNDA2861A
- Z-1707-2026 · Open, ClassifiedTHORACIC ROBOTS, DYNJ908777B
- Z-1708-2026 · Open, ClassifiedMedline kits containing Olympus biopsy valves: 1. BAL KIT, DYNDA2137B 2. ENDO KIT, DYKE1915
- Z-1710-2026 · Open, ClassifiedMedline kits containing Olympus biopsy valves: 1. BRONCH PROCEDURE KIT, DYKE2091 2. BRONCHSCOPY, DYNJ900898G DYNJ901922I 3. BRONCHSCOPY PACK, DYNJ38313B 4. BRONCHOSCOPY PACK 0…
- Z-1711-2026 · Open, ClassifiedMEDLINE ANTERIOR HIP PACK DYNJ64672B
Sources and updates
- Recall record: FDA Medical Device Recalls, file dated Oct 16, 2026 · View the FDA recall notice ↗
- Devices: FDA GUDID, file dated Oct 13, 2026. Devices are linked when their identifier (with a valid check digit) appears in the recall's code information.
- Page last rebuilt: Oct 16, 2026. Text above is shown as published by the FDA.
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