Cardinal Health 200, LLC: Medical Device Recall in 2019 - (Recall #: Z-2051-2019)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2019.

Data Source: FDA.

Product Description:

Monoject Blunt Cannula, 20 G x 1-1/2" (0.902 mm x 3.8 cm) Item code: 8881202363

Product Classification:

Class II

Date Initiated: April 30, 2019

Date Posted: July 31, 2019

Recall Number: Z-2051-2019

Event ID: 82927

Reason for Recall:

Manufacturing defect was found for the cartridge component, which could compromise the sterility barrier of the product

Status: Completed

Product Quantity: N/A

Code Information:

Lot Number: 907734

Distribution Pattern:

Nationwide Foreign: AU, BE, CA, DK, FI, GB, IE, NL

Voluntary or Mandated:

Voluntary: Firm initiated