Plastics TRAY Recall: Contamination
PLASTICS TRAY; Model/Item Number (Kit): EURO053;
What is the FDA recall status?
The FDA record lists this recall as ongoing. FDA enforcement data is not a live recall-lifecycle tracker. Follow the official instructions and check the agency notice or firm for current guidance.
Why was Plastics TRAY recalled?
Product may be potentially contaminated with a lubricant used during the manufacturing process.
What should I do if I have this product?
Follow the firm and FDA instructions for the affected product. Contact the recalling firm for current guidance.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare your product with the product description and available lot, UPC or model codes below from the official FDA record to check whether it is covered by this recall. If an identifier is missing or unclear, check the complete official notice or contact the firm; an incomplete match here does not establish that your product is unaffected.
Which lot codes, UPCs or models are affected?
Model/Item Number (Kit): EURO053; UDI-DI: 10809160423813; Kit Lot Numbers: 1674613; Recalled Supplier Component (in kit): A902416; Recalled Supplier Lot Number (in kit): NGKU3975;
- Agency record number
- Z-0100-2027
- Product
- PLASTICS TRAY; Model/Item Number (Kit): EURO053;
- Recalling firm
- AVID Medical, Inc.
- Quantity
- 28
- Distribution
- US Nationwide distribution in the states of AZ, CA, FL, MD, NE, TX.
- Recall started
- August 10, 2026
- Report date
- October 14, 2026
- Classification
- Class II
- Status
- Ongoing
- Agency
- FDA (device)