ARTHROSCOPY Convenience kit used for surgical recall
ARTHROSCOPY Convenience kit used for surgical procedures, SKU SYNJ910004C
Why was ARTHROSCOPY Convenience kit used for surgical recalled?
Products within a Medline pack may be impacted by a packaging error in which an incomplete seal has formed on the packaging thereby creating a packaging seal gap.
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?
UDI-DI: 10195327246747; Lot Numbers: 24GBI464 24HBO800
- Product
- ARTHROSCOPY Convenience kit used for surgical procedures, SKU SYNJ910004C
- Recalling firm
- MEDLINE INDUSTRIES, LP - Northfield
- Quantity
- 80 units
- Distribution
- US Nationwide distribution in the state of TN.
- Recall date
- November 20, 2024
- Classification
- Class II
- Status
- Ongoing
- Agency
- FDA (device)