- 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)
- EBSI1705A UDI-DI 10653160382850 Lot 2025103090 EBSI1057A UDI-DI 10653160356875 Lot 2025120890 EBSI1498 UDI-DI 10193489111538 Lot 2025110690 EBSI1585 UDI-DI 10653160354796 Lot 2025102190 EBSI1621 UDI-DI 10653160358336 Lot 2025110390 EBSI1837 UDI-DI 10653160388555 Lot 2025102990
- 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-2438-2026
- 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