Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Myelotec Video Guided Catheters Recalled by Myelotec, Inc. Due to Obstructed/blocked port from defective VGC Access Port Body...
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 Myelotec, Inc. directly.
Affected Products
Myelotec Video Guided Catheters, REF 2010 3.0 mm OD x 30 Cm Working Length, Two 1.3mm Working Channels
Quantity: 2980 units
Why Was This Recalled?
Obstructed/blocked port from defective VGC Access Port Body component.
Where Was This Sold?
This product was distributed to 5 states: CA, FL, KY, MN, NJ
About Myelotec, Inc.
Myelotec, Inc. has 1 total recall tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report