Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Medline CHEST TUBE REORDER NO: DYNJ36762A Recalled by Medline Industries Inc. Due to Due to a non-sterile component (tape) being place...
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 Medline Industries Inc. directly.
Affected Products
Medline CHEST TUBE REORDER NO: DYNJ36762A
Quantity: 300 kits
Why Was This Recalled?
Due to a non-sterile component (tape) being place within the sterile portion of the Chest Tube Convenience Kit
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Medline Industries Inc.
Medline Industries 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