Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
RadiaLux Lighted Retractor (Pink) Recalled by Medtronic Navigation, Inc. Due to Defect in sterile pouch seal, incomplete seal, of...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Medtronic Navigation, Inc. directly.
Affected Products
RadiaLux Lighted Retractor (Pink), REF: 50-101-1
Quantity: 2317
Why Was This Recalled?
Defect in sterile pouch seal, incomplete seal, of lighted Retractors, increases the risk of contamination, which can lead to post-operative infection.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Medtronic Navigation, Inc.
Medtronic Navigation, Inc. has 91 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report