FDA-Device2024-10-23Class II
MEDLINE OPEN HEART, REF DYNJ904261B
MEDLINE INDUSTRIES, LP - Northfield
Hazard
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.
Sold states
US Nationwide distribution.
Affected count
30 units
Manufactured in
3 Lakes Dr, Northfield, IL, United States
Products
MEDLINE OPEN HEART, REF DYNJ904261B
Official notice
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0122-2025Don't want to check this manually?
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