Wound Dressing Kit
Recall Summary Medline is recalling Cervical Pack wound dressing kits (Kit Number DYNJ37902F) distributed worldwide because testing found higher-than-expected endotoxin levels on the neuro sponges, meaning the product may not meet safety specifications. Endotoxins are bacterial substances that can cause adverse reactions if they come into contact with open wounds or internal tissues. This recall affects medical facilities and healthcare providers who received these kits.
- Product
- Medline medical procedure kits, containing Medline Neuro Sponges, labeled as follows: CERVICAL PACK, Medline Kit Number/SKU DYNJ37902F
- 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/e2f385c8-37a7-4486-972a-123b7a75635a