Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Medline Convenience Kits for Various Procedures: 1) CLOVIS RESP/INTUB DRAWER 2 Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to Kits contain recalled components due to reports 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 MEDLINE INDUSTRIES, LP - Northfield directly.
Affected Products
Medline Convenience Kits for Various Procedures: 1) CLOVIS RESP/INTUB DRAWER 2, Model Number ACC010809; 2) RESP/INTUBATION DRAWER #2, Model Number ACC010813
Quantity: 0 kits
Why Was This Recalled?
Kits contain recalled components due to reports of reduced skin barrier wear time. This refers to a shorter duration that a skin barrier can effectively adhere to and protect the skin before it needs to be replaced.
Where Was This Sold?
This product was distributed to 2 states: CA, NY
About MEDLINE INDUSTRIES, LP - Northfield
MEDLINE INDUSTRIES, LP - Northfield has 822 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report