Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
MEDLINE KIT CV I II Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to Medline Industries, LP. has identified certain kits containing...
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 KIT CV I II, REF DYNJ906071B
Quantity: 56 kits
Why Was This Recalled?
Medline Industries, LP. has identified certain kits containing the recalled Medtronic lots of the DLP Vessel Cannulae. During manufacturing of the three listed lot numbers, product for model 30001 was incorrectly labeled as model 30000.
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