FDA-Device2026-10-14Class IIPROCESSING DEFECT
AVID Medical EURO053 plastic tray recalled for manufacturing lubricant contamination
What this means
AVID Medical's EURO053 plastic tray (a medical device kit component) may be contaminated with lubricant residue from manufacturing. The contamination affects 28 units distributed across six U.S. states.
- Check if you have the EURO053 kit with lot number 1674613 or the A902416 component with lot number NGKU3975.
- Do not use the affected product.
- Contact AVID Medical or your healthcare provider for return or replacement instructions.
The agency's original wording
Hazard
Product may be potentially contaminated with a lubricant used during the manufacturing process.
Intended for
Adults
Illnesses reported
None reported
Sold states
US Nationwide distribution in the states of AZ, CA, FL, MD, NE, TX.
Affected count
28
Manufactured in
9000 Westmont Dr, N/A, Toano, VA, United States
Products
PLASTICS TRAY; Model/Item Number (Kit): EURO053;
Official notice
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0100-2027More AVID Medical recalls
- FDA-Device2026-10-14AVID Medical HEART PREP TRAY recalled for potential manufacturing lubricant contamination
- FDA-Device2026-10-14AVID Medical PACK OPEN HEART CFH recalled for potential manufacturing lubricant contamination
- FDA-Device2026-10-14AVID Medical laparoscopic prostatectomy kit recalled for manufacturing lubricant contamination
- FDA-Device2026-10-14AVID Medical Endovascular Pack recalled for manufacturing lubricant contamination
- FDA-Device2026-10-14AVID Medical DAVINCI LAP/GYN surgical kit recalled for manufacturing lubricant contamination
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