Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Medline medical procedure kits labeled as follows: a) HEART ANESTHESIA SET UP Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to A slight dimensional variation which has the potential...
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 medical procedure kits labeled as follows: a) HEART ANESTHESIA SET UP, REF DYNJ902752C, b) KIT ENDO, REF DYKE1872A, c) LOWER ENDO KIT, REF DYKE1921A, d) PACEMAKER, REF DYNJ901681D, e) UPPER ENDO KIT, REF DYKE1922A, f) VASCULAR, REF DYNJ905515D, g) VASCUALR, REF DYNJ902387K, h) VASCULAR III, REF DYNJS2035C
Quantity: 26096 units
Why Was This Recalled?
A slight dimensional variation which has the potential for increased difficulty fitting into outer canister.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
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