FDA Medical devices recall ·
Sterile Medline Convenience Kits: 1) EXTREMITY PACK… recall
This is an FDA Class I recall — the most serious type.
- Recall number
- Z-2593-2025
- Date
- (initiated August 8, 2025)
- Company / brand
- Medline Industries, LP
3 Lakes Dr, Northfield, IL, United States - Category
- Medical devices › Class I
- Classification
- Class I
- Status
- Ongoing
- Units affected
- 88 units
- Hazard tags
- Sterility
- Initiated by
- Voluntary: Firm initiated
Read the official FDA notice ↗
Product
Sterile Medline Convenience Kits: 1) EXTREMITY PACK, Model Number: DYNJ45701B
Why was it recalled?
Convenience kits labeled as sterile have not gone through the sterilization process.
What should you do?
FDA enforcement reports do not list a consumer remedy. Check the product codes below against what you have; if it matches, stop using it and follow the instructions in the firm's or FDA's official notice, or contact the company. If you have health concerns, contact your healthcare provider.
Product codes & lot numbers
1) DYNJ45701B, UDI-DI: 10193489856279(each), 40193489856270(case), Lot Number: 25GBF686
Distribution
US Distribution to States of: FL, MD, NJ, TN
States: Florida Maryland New Jersey Tennessee
What does Class I mean?
Class I is the most serious FDA recall class: there is a reasonable probability that using or being exposed to the product will cause serious adverse health consequences or death.
Source: FDA (medical devices), recall Z-2593-2025. Official notice. Republished from public data; RecallFlag is not affiliated with the FDA.