Recall Z-2593-2025— Medline Industries, LP
Class I · Ongoing
Class I FDA medical device recall by Medline Industries, LP, initiated 2025-08-08. FDA's recall record names no specific 510(k) clearance for this event. Product: Sterile Medline Convenience Kits: 1) EXTREMITY PACK, Model Number: DYNJ45701B. Reason: Convenience kits labeled as sterile have not gone through the sterilization process..
- Recalling firm
- Medline Industries, LP
- Classification
- Class I
- Status
- Ongoing
- Initiated
- 2025-08-08
- Firm location
- Northfield, IL, United States
Product description
Sterile Medline Convenience Kits: 1) EXTREMITY PACK, Model Number: DYNJ45701B
Reason for recall
Convenience kits labeled as sterile have not gone through the sterilization process.
Data sourced from openFDA. This site is unofficial and independent of the FDA.