Spinal Epidural Anesthesia Kit
Recall Summary Medline's Femoral Block Tray kits (model DYNJRA1739B) are being recalled because they contain a recalled adhesive product that may cause tubing to crack when used, making the kit unsuitable for application. The recall affects kits distributed nationwide across all U.S. states and territories. This is a Class II recall affecting medical devices.
- Product
- Medline convenience kits: FEMORAL BLOCK TRAY DYNJRA1739B
- Reason
- Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.
- Classification
- Class II
- Category
- medical device recall
- Country
- United States
- Agency
- FDA-DEVICES
- Recall date
- 2026-04-27
- Status
- Open, Classified
- Areas affected
- AL, AK, AZ, AR, CA, CO, CT, DE, FL, GA, HI, ID, ...
- Distribution
- US Nationwide distribution. OUS distribution pending.
Official recall notice from FDA-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/1a2ddd78-8a49-4533-af25-b9b6b57b0f5e