- Recalling firm
- Medline Industries, LP
- 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.
- Affected products (lot / model / serial)
- DYNDC2356B UDI-DI 10653160327271 Lot 2025102090 DT17570 UDI-DI 10653160266891 Lot 2025102290 DT21370B UDI-DI 10653160360643 Lot 2025102290 DT21115B UDI-DI 10653160360681 Lot 2025111490 DYNDC2815A UDI-DI 10653160357070 Lot 2025110590
- Units affected
- 49,654 kits total
- Distribution pattern
- US Nationwide distribution. OUS distribution pending.
- Firm location
- Northfield, IL, United States
- Recall type
- Voluntary: Firm initiated
- How the firm notified customers
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Product type
- Devices
- Status
- Ongoing
- Recall number
- Z-2437-2026
- Recall initiated
- April 27, 2026
- FDA classification date
- June 12, 2026
- FDA report date
- June 24, 2026
- FDA event ID
- 98951
- Last updated on HTM Vibe
- July 23, 2026