Is my kit affected by this recall?

Kits specifically named in the recall are BAL KIT, DYNDA2137B and ENDO KIT, DYKE1915 with the associated UDI-DI and LOT codes listed in the recall. If your kit matches those identifiers, it is affected.

What should I do if I have one of these kits?

Stop using the kit immediately. Follow the recall instructions issued by Medline and the manufacturer. Contact Medline or your healthcare provider for next steps.

What is the hazard from the recalled valves?

Rubber fragments can detach from the valve slit, potentially causing a foreign body in a patient’s tracheobronchial tree and may require removal.

Are there any reported injuries?

No injuries or incidents have been reported in the recall notice.

Will I receive a refund or replacement?

The recall states that a remedy is available. Contact Medline or your healthcare provider for instructions on refunds or replacements.

How can I verify the model or lot numbers?

Check the kit label for BAL KIT, DYNDA2137B or ENDO KIT, DYKE1915 and compare with the UDI-DI and LOT codes listed in the recall.

Where can I find official recall information?

See the FDA enforcement report Z-1708-2026 linked in the recall notice.

How long does it take to process refunds or replacements?

Companies typically process refunds or replacements within several weeks; the recall notes general timelines may apply.

What if the facility is slow to respond?

Document all communications and escalate to Medline’s recall contact or FDA channels if needed.

Should I discard the kit or keep it for evidence?

Follow Medline’s guidance. Do not use the kit, and preserve related documentation and packaging as part of your records.

What about future purchases of similar devices?

Verify UDI-DI and LOT codes before purchase and ensure vendor recalls are checked during procurement.

Who should I contact for medical concerns related to exposure?

Consult a healthcare professional for evaluation if exposure occurs during a procedure.

HIGHFebruary 16, 2026

Medline Recalls 14,379 Olympus Biopsy Valve Kits in 2026

Medline Industries, LP recalled 14,379 kits nationwide that include Olympus biopsy valves. The recall concerns rubber fragments detaching in the slit of single-use biopsy valves. Stop using these kits immediately and follow manufacturer instructions for return or replacement.

Quick Facts at a Glance

Recall Date: February 16, 2026
Hazard Level: HIGH
Brand: Medline
Category: Health & Personal Care
Sold At: Multiple Retailers
Geographic Scope: 1 states
At-Risk Groups: GENERAL

Hazard Information

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

Patients and healthcare providers should stop using this device immediately. Follow the recall instructions provided by the manufacturer. Contact Medline Industries, LP or your healthcare provider for instructions

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About This Product

These kits are used in medical procedures and incorporate Olympus biopsy valves that are designed for single-use applications.

Why This Is Dangerous

Rubber fragments detaching from the valve slit can become a foreign body in the tracheobronchial tree, potentially causing inflammation, hypoxia, or extended procedures.

Industry Context

This recall is not described as part of a broader industry pattern in the notice.

Real-World Impact

The recall may disrupt procedures in affected facilities and obligate immediate use of alternative devices or replacements.

Practical Guidance

How to identify if yours is affected

Identify BAL KIT, DYNDA2137B or ENDO KIT, DYKE1915 on the kit label.
Check associated UDI-DI and LOT numbers: 10195327501259 (EA) 40195327501250 (CS) with LOTS 24DBW065 24EBV301 24HBB492 24JBW143 25ABG569 25CBH359 25DBD213 25GBP569 25HBQ088 25KBF725 26ABE643; and 10195327371029 (EA) 40195327371020 (CS) with LOTS 24FBM018 24GBL319.
Check packaging for recall notices and refer to the FDA enforcement page for recall Z-1708-2026.

Where to find product info

UDI-DI and LOT codes are printed on the kit label and packaging. Manufacturer recall notices and FDA enforcement pages provide official guidance.

What timeline to expect

Refunds or replacements typically take 4-8 weeks once approved by the recall administrator.

If the manufacturer is unresponsive

Document all attempts to contact Medline or the recalling authority.
Escalate to hospital/clinic compliance teams for formal recall coordination.
If necessary, contact FDA via the recall or MedWatch channels for escalation.

How to prevent similar issues

In future purchases, verify UDI-DI and LOT numbers before procurement.
Prefer vendors that provide clear recall status on packaging.
Maintain updated recall databases for medical devices used in your facility.

Documentation advice

Retain recall notices, correspondence with Medline, the kit packaging, and any related medical records showing exposure or remediation steps.

Product Details

Kits: BAL KIT, DYNDA2137B and ENDO KIT, DYKE1915. Sold nationwide in the United States. Recall date: 2026-02-16. Quantity: 14,379 kits. Brands involved: Medline; Olympus biopsy valves. Model identifiers: UDI-DI 10195327501259 (EA) 40195327501250 (CS) with LOTS 24DBW065 24EBV301 24HBB492 24JBW143 25ABG569 25CBH359 25DBD213 25GBP569 25HBQ088 25KBF725 26ABE643 and UDI-DI 10195327371029 (EA) 40195327371020 (CS) with LOTS 24FBM018 24GBL319.

Reported Incidents

No injuries or incidents have been reported.

Key Facts

14,379 total kits recalled
Kits include BAL KIT DYNDA2137B and ENDO KIT DYKE1915
Distribution: nationwide in 13 states plus unspecified nationwide reach
Model/Lot details provided as UDI-DI and LOT codes
Immediate action recommended: stop use and follow recall instructions

View Original Recall on FDA - Medical Devices

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Safety Guide

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Safety Assessment

Risk LevelHIGH

Severity Score

8/ 10

Affected Groups

GENERAL

Injury Types

CHOKINGSUFFOCATIONOTHER

Product Classification

CategoryHealth & Personal Care › Medical Devices

Product TypeBiopsy Valve Kit

Product Details

Jul 25, 2025

Medline

Medline Industries,