Medline Industries, LP: Device Recall
Recall #Z-1196-2026 · 12/12/2025
Class II: Risk
Recall Details
- Recall Number
- Z-1196-2026
- Classification
- Class II
- Product Type
- Device
- Recalling Firm
- Medline Industries, LP
- Status
- Ongoing
- Date Initiated
- 12/12/2025
- Location
- Northfield, IL, United States
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 236 units
Reason for Recall
Medline kits were manufactured and distributed containing MASTISOL liquid adhesive which was recalled due to complaints that the butyrate tubing cracked during actuation of the vials of MASTISOL Liquid Adhesive.
Product Description
Medline medical procedure convenience kits labeled as: 1) DEPAUL BASIC NEURO-LF, Kit SKU DYNJ20028L; 2) NEURO MINOR PACK, Kit SKU DYNJ46546M; 3) NEURO SHUNT PACK, Kit SKU DYNJ54396K; 4) NEURO PACK, Kit SKU DYNJ59397Q; 5) NEURO BASIC, Kit SKU DYNJ904052L; 6) PK NEURO SHUNT BUMC, Kit SKU DYNJT6428.
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.