Cardinal Health: Medical Device Recall in 2021 - (Recall #: Z-2286-2021)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2021.

Data Source: FDA.

Product Description:

Monoject 0.9% Sodium Chloride Flush Syringe, 5mL Fill, STERILE, Product Code 8881570125 The proposed device is indicated for use in flushing compatible intravenous tubing systems and indwelling intravascular access devices.

Product Classification:

Class I

Date Initiated: August 4, 2021

Date Posted: September 1, 2021

Recall Number: Z-2286-2021

Event ID: 88421

Reason for Recall:

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

Status: Ongoing

Product Quantity: 267,217,860 eaches in total

Code Information:

20D0614 21D0894 20D0624 20D0674 20D0684 20H1504 20H1514

Distribution Pattern:

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.

Voluntary or Mandated:

Voluntary: Firm initiated