Z-2432-2026 Class II Ongoing
FDA device recall Z-2432-2026 was initiated by Medline Industries, LP on April 27, 2026 and is designated Class II. Reason for recall: Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application. The recall status is ongoing. Affected quantity: 49,654 kits total.
Recall Details
- Product Type
- Devices
- Report Date
- June 24, 2026
- Initiation Date
- April 27, 2026
- Termination Date
- N/A
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 49,654 kits total
Product Description
Medline convenience kits: C-SECTION KIT DYNJ904305J C-SECTION PACK DYNJ69533C
Reason for Recall
Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.
Distribution Pattern
US Nationwide distribution. OUS distribution pending.
Code Information
DYNJ904305J UDI-DI 10198459268151 lot 25KBT972 DYNJ69533C UDI-DI 10198459524097 lot 26BBC483