Nerve Block Tray
Recall Summary Medline is recalling two nerve block procedure kits (NEURO PACK and CRANIO/NEURO/SPINE) that contain neuro sponges with higher-than-expected endotoxin levels, which are bacterial contaminants that can cause immune responses. The affected kits were distributed worldwide to hospitals and medical facilities. This is a Class II recall, meaning the products could cause adverse health effects but are unlikely to cause serious injury.
- Product
- Medline medical procedure kits, containing Medline Neuro Sponges, labeled as follows: 1. NEURO PACK, Medline kit number/SKU DYNJ64479; 2. CRANIO/NEURO/SPINE, Medline kit number/SKU DYNJ901072D.
- Reason
- During an internal review, Medline identified higher-than-expected endotoxin levels on a representative Medline neuro sponge product, indicating that in-market product may be out-of-specification for endotoxin.
- Classification
- Class II
- Category
- medical device recall
- Country
- United States
- Agency
- FDA-DEVICES
- Recall date
- 2026-03-19
- Status
- Open, Classified
- Distribution
- Worldwide distribution.
Official recall notice from FDA-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/a22a51bd-e9bf-4053-89c3-596457a4bd1c