Deroyal Tracecart Shoulder Arthroscopy Tracecart recall
DeRoyal TRACECART SHOULDER ARTHROSCOPY TRACECART, REF 53-1962.02
Why was Deroyal Tracecart Shoulder Arthroscopy Tracecart recalled?
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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?
Lot Numbers: 56296761 exp 10/01/2023; 56717318 exp 11/01/2023; 57136671 exp 11/01/2023; 57225673 exp 11/01/2023; 57225817 exp 02-01-2024; 57455920 exp 02-01-2024; 57646161 exp 02-01-2024; 57889699 exp 02-01-2024; 58003853 exp 02-01-2024
- Product
- DeRoyal TRACECART SHOULDER ARTHROSCOPY TRACECART, REF 53-1962.02
- Recalling firm
- DeRoyal Industries Inc
- Quantity
- 117 kits
- Distribution
- US: Tennessee, Texas, New York, Wisconsin, Florida, Virginia, Massachusetts, Arizona, Missouri, Connecticut, New Jersey, Pennsylvania, North Carolina, Louisiana, Michigan, Minnesota, Ohio, Indiana, Kansas, Illinois, Alabama, Georgia, Mississippi
- Recall date
- December 21, 2022
- Classification
- Class II
- Status
- Ongoing
- Agency
- FDA (device)