Medline Kits: 1) ARTHROSCOPY PACK recall
Medline Kits: 1) ARTHROSCOPY PACK, Model Number: DYNJ82440
Why was Medline Kits: 1) ARTHROSCOPY PACK recalled?
The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.
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) DYNJ82440, UDI-DI: 10195327196240(each), 40195327196241(case), Lot Number: 24BMD005
- Product
- Medline Kits: 1) ARTHROSCOPY PACK, Model Number: DYNJ82440
- Recalling firm
- Medline Industries, LP
- Quantity
- 27 units
- Distribution
- US Nationwide distribution.
- Recall date
- April 29, 2026
- Classification
- Class II
- Status
- Ongoing
- Agency
- FDA (device)