FDA-Device2026-06-24Class IIPACKAGING DEFECT
Medline nerve block kits recalled for cracked tubing in adhesive component
What this means
Medline Industries nerve block kits contain a recalled adhesive component from Ferndale Laboratories. The tubing in these kits may crack when used, making the product unable to function properly for patient care.
- Check your inventory for affected lot numbers: DYNJRA2119A (lot 25LBB738) and DYNJRA1011A (lots 25KBB849 and 25LBB734)
- Stop using affected kits immediately
- Contact Medline Industries or your supplier for instructions on return or replacement
The agency's original wording
Hazard
Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.
Intended for
Adults
Illnesses reported
None reported
Sold states
US Nationwide distribution. OUS distribution pending.
Affected count
49,654 kits total
Manufactured in
3 Lakes Dr, Northfield, IL, United States
Products
BLOCK TRAY DYNJRA2119A INDWELLING NERVE BLOCK DYNJRA1011A
Official notice
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2416-2026More Medline recalls
- FDA-Device2026-09-09Medline Convenience Kits recalled for potential sterility breach in antiseptic applicators
- FDA-Device2026-09-09Medline Convenience Kits with BD ChloraPrep Clear applicators recalled for contamination risk
- FDA-Device2026-09-09Medline Convenience Kits recalled for sterility packaging breach risk
- FDA-Device2026-09-09Medline Convenience Kits with BD ChloraPrep Clear applicators recalled for defective packaging seals
- FDA-Device2026-09-09Medline Arterial Line Insertion Kit recalled for sterility packaging breach risk
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