FDA-Device2024-10-23Class II
MEDLINE KIT CV I II, REF DYNJ906071B
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
56 kits
Manufactured in
3 Lakes Dr, Northfield, IL, United States
Products
MEDLINE KIT CV I II, REF DYNJ906071B
Official notice
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0123-2025Don't want to check this manually?
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