Sterile Medline Convenience Kits: 1) EXTREMITY PACK recall
Sterile Medline Convenience Kits: 1) EXTREMITY PACK, Model Number: DYNJ45701B
Why was Sterile Medline Convenience Kits: 1) EXTREMITY PACK recalled?
Convenience kits labeled as sterile have not gone through the sterilization process.
What should I do if I have this product?
The recall is ongoing. Follow the firm and FDA instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
1) DYNJ45701B, UDI-DI: 10193489856279(each), 40193489856270(case), Lot Number: 25GBF686
- Product
- Sterile Medline Convenience Kits: 1) EXTREMITY PACK, Model Number: DYNJ45701B
- Recalling firm
- Medline Industries, LP
- Quantity
- 88 units
- Distribution
- US Distribution to States of: FL, MD, NJ, TN
- Recall date
- October 8, 2025
- Classification
- Class I
- Status
- Ongoing
- Agency
- FDA (device)