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RecallWatchMedical Device Safety
Class IIOngoingZ-1710-2026

Medline Industries, LP recalls Medline kits containing Olympus biopsy valves: 1. BRONCH PROCEDURE KIT

Medline Industries, LPNorthfield, IL, United StatesReported Apr 8, 2026 · 3 months ago
Legal News Analyst ·

Reason for recall

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.

Affected product

Check your device

Enter a lot, serial, REF, or UDI number from your device's label to check it against this recall's listed codes.

Affected products & lots

  • Medline kits containing Olympus biopsy valves: 1. BRONCH PROCEDURE KIT, DYKE2091 2. BRONCHSCOPY, DYNJ900898G DYNJ901922I 3. BRONCHSCOPY PACK, DYNJ38313B 4. BRONCHOSCOPY PACK 0120367-LF, DYNJ32750G DYNJ32750I 5. KIT, WR THORACIC, DYNJ911252 6. LARYNGOSCOPY/BRONCHOSCOPY PACK, DYNJ58146B 7. LEX THORACIC, DYNJ902016K DYNJ902016L 8. ORGAN PROCUREMENT, DYNJ908686 9. PULMONARY PACK, DYKE1859 10. THORACIC, DYNJ901666L 11. THORACIC ROBOTICS, DYNJ908777A 12. THORACOTOMY/THORACOSCOPY, DYNJ900482N DYNJ900482O 13. XPSDYNJ907605
    UDI-DI 10198459606397
    148 affected lots
    25LBR616DYNJ900898G101953274794734019532747947423JBI82423KBJ53524ABR78924ABV917
    +140 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

What the firm 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.

DistributionShow details

US Nationwide distribution in the states of CA, FL, IL, IN, KY, MA, MD, MT, NY, OH, PA, TN, TX.

Class IIWhat this means

Use of the product may cause temporary or medically reversible adverse health consequences.

Sources & references

Source: U.S. FDA openFDA device enforcement reports. This summary is informational and may lag or differ from the official record. Always verify against the FDA before acting.

Taylor Coteus
Legal News Analyst

Taylor Coteus is RecallWatch's Legal News Analyst, covering FDA medical-device enforcement and patient-safety litigation. He reviews every recall against the FDA's official openFDA record before it is published and is responsible for corrections and editorial accuracy.

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