# FDA recall Z-1710-2026

> **Medline Industries, LP** · Class II · device recall initiated 2026-02-16.

## Product

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. XPS, DYNJ907605

## 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.

## Distribution

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

## Key facts

- **Recall number:** Z-1710-2026
- **Recalling firm:** Medline Industries, LP
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2026-02-16
- **Report date:** 2026-04-08

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Northfield, IL, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1710-2026

## Citation

> AI Analytics. FDA recall Z-1710-2026. Retrieved 2026-08-11 from https://api.ai-analytics.org/recall/Z-1710-2026. Source: US FDA. Licensed CC0.

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