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Cardinal Health recalls Monoject 0.9% Sodium Chloride Flush Syringe, 3 mL Fill, STERILE, Product Code 8881570123 The proposed device is indi

Recalled September 1, 2021 · FDA recall Z-2285-2021 · Cardinal Health

Hazard
Potential for the plunger to draw back after the air has been expelled and reintroduce air back into the syringe. · FDA Class I
Units
267,217,860 eaches in total
Sold at
US Nationwide Distribution:  AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, PI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV and WY.

Description

Potential for the plunger to draw back after the air has been expelled and reintroduce air back into the syringe.

Product
Monoject 0.9% Sodium Chloride Flush Syringe, 3 mL Fill, STERILE, Product Code 8881570123 The proposed device is indicated for use in flushing compatible intravenous tubing systems and indwelling intravascular access devices.
Manufacturer(s)
Cardinal Health

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

Cardinal Health recalls Monoject 0.9% Sodium Chloride Flush Syringe, 3 mL Fill, STERILE, Product Code 8881570123 The proposed device is indi | RecallWatchUSA