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Magnolia Medical Technologies, Inc. recalls The Steripath Gen2 Blood Collection System Model Number/Description 2700-21-EN / Steripath Gen2 Blood Collection Sys
Recalled December 8, 2021 · FDA recall Z-0318-2022 · Magnolia Medical Technologies
Hazard
Due to an uptick of complaints associated with premature needle retraction of blood collection system. · FDA Class II
Units
137,200 devices
Sold at
U.S. Nationwide distribution in the states of MD, WV, DE, VA, DC, IN, MI, MA, SC, NY, IL, TX, AL, OK, GA, NE, FL, MO, CA, CO, NM, AR, WY, KS, PA, WA, MT, and AZ.
Description
Due to an uptick of complaints associated with premature needle retraction of blood collection system.
Product
The Steripath Gen2 Blood Collection System Model Number/Description 2700-21-EN / Steripath Gen2 Blood Collection System - 21G, Wide Neck 2700-23-EN / Steripath Gen2 Blood Collection System - 23G, Wide Neck 27BD-21-EN / Steripath Gen2 Blood Collection System - 21G, Long Neck 27BD-23-EN / Steripath Gen2 Blood Collection System - 23G, Long Neck
Manufacturer(s)
Magnolia Medical Technologies, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →