Cardinal Health 200, LLC: Medical Device Recall in 2020 - (Recall #: Z-1453-2020)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2020.

Data Source: FDA.

Product Description:

Monoject 3mL Syringe with Hypodermic Safety Needle, 22G x 1-1/2 . Item Code 11832215 - Product Usage: used for general purpose injection and aspiration of fluids from vials, ampules and parts of the body below the surface of the skin.

Product Classification:

Class II

Date Initiated: January 15, 2020

Date Posted: March 18, 2020

Recall Number: Z-1453-2020

Event ID: 84779

Reason for Recall:

Non-sterile product was shipped to customers. Product package is labeled as both "STERILE" and "NON-STERILR" ; the product did not undergo sterilization process and is non-sterile. The usage of a needle that is not sterile could result in infection. Firm is not aware of any reports of patient harm.

Status: Terminated

Product Quantity: 8400 each

Code Information:

Lot No. 15072015, Item Code 11832215 , Expires 06/20/2020.

Distribution Pattern:

Worldwide distributions - US Nationwide distributions in the states of 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, SC, SD, TN, TX, UT, VA, WA, WI, WV, and countries of Canada, Australia, South Africa, Belgium, Germany, Ireland, Portugal Spain, and UK.

Voluntary or Mandated:

Voluntary: Firm initiated