Medline Industries, Lp: Tourniquet, Pneumatic
Recall Summary Medline Industries is recalling a foot and ankle convenience kit (SKU DYNJ65395A) that contains a pneumatic tourniquet because one of its components has an incorrect shelf-life marking. The kit was distributed nationwide across all U.S. states and Washington, D.C. This is a Class I recall, the FDA's most serious classification.
- Recalling firm
- Medline Industries, LP
- Product
- Medline convenience kit labeled as: FOOT ANKLE. Medline Kit SKU DYNJ65395A
- Reason
- Discrepancy in the shelf-life of a component
- Classification
- Class I
- Category
- medical device recall
- Country
- United States
- Agency
- FDA-DEVICES
- Recall date
- 2026-09-11
- Status
- Open, Classified
- Areas affected
- AL, AK, AZ, AR, CA, CO, CT, DE, FL, GA, HI, ID, ...
- Distribution
- US Nationwide distribution in the state of NY.
Official recall notice from FDA-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/bf13cd2f-7430-41f5-8e9d-c5226e8edd85