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Cardinal Health 200, LLC recalls McKesson PREVENT M NEEDLE (Magellan Technology) 25G X 5/8". A single lumen needle intended to inject fluids into, or w

Recalled March 24, 2021 · FDA recall Z-1251-2021 · Cardinal Health 200

Hazard
Safety shield not locking into the cannula. If the safety shield activation fails to lock a contaminated needle, a needlestick may occur and there is the potential for exposure to bloodborne pathogens · FDA Class II
Units
108,000 units
Sold at
Worldwide distribution - US Nationwide distribution and the countries of AE, Japan.

Description

Safety shield not locking into the cannula. If the safety shield activation fails to lock a contaminated needle, a needlestick may occur and there is the potential for exposure to bloodborne pathogens

Product
McKesson PREVENT M NEEDLE (Magellan Technology) 25G X 5/8". A single lumen needle intended to inject fluids into, or withdraw fluids from, parts of the body below the surface of the skin. Product Code: 26558
Manufacturer(s)
Cardinal Health 200, LLC

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov

Cardinal Health 200, LLC recalls McKesson PREVENT M NEEDLE (Magellan Technology) 25G X 5/8". A single lumen needle intended to inject fluids into, or w | RecallWatchUSA