Medline Industries, LP: Device Recall
Recall #Z-1085-2026 · 12/16/2025
Class II: Risk
Recall Details
- Recall Number
- Z-1085-2026
- Classification
- Class II
- Product Type
- Device
- Recalling Firm
- Medline Industries, LP
- Status
- Ongoing
- Date Initiated
- 12/16/2025
- Location
- Northfield, IL, United States
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 96 units
Reason for Recall
Medline kits containing Stryker's Strykeflow 2 Suction Irrigators due to a change in design in 2024, irrigation solution is able to travel to the handpiece and battery pack during use of the Strykeflow 2 Suction Irrigator. This design change has caused some devices to leak and/or emit vaporized saline (which can resemble smoke) during use.
Product Description
Medline medical procedure convenience kits labeled as: 1) THORACIC ROBOTICS, REF DYNJ908777B; 2) CARDIAC ROBOTIC WHC KIT-LF, REF DYNJ911359
Distribution Pattern
US Nationwide distribution.
Other Recalls by Medline Industries, LP
- Class II: Risk 12/16/2025
- Class II: Risk 12/16/2025
- Class II: Risk 12/16/2025
- Class II: Risk 12/16/2025
- Class II: Risk 12/16/2025
Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.