PlainRecalls
FDA Devices Moderate Class II Completed

Monoject Standard Hypodermic Needle, 20 G x 1-1/2" bulk Item code: 8881200664

Reported: July 31, 2019 Initiated: April 30, 2019 #Z-2042-2019

Product Description

Monoject Standard Hypodermic Needle, 20 G x 1-1/2" bulk Item code: 8881200664

Reason for Recall

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

Details

Recalling Firm
Cardinal Health 200, LLC
Units Affected
N/A
Distribution
Nationwide Foreign: AU, BE, CA, DK, FI, GB, IE, NL
Location
Mansfield, MA

Frequently Asked Questions

What product was recalled?
Monoject Standard Hypodermic Needle, 20 G x 1-1/2" bulk Item code: 8881200664. Recalled by Cardinal Health 200, LLC. Units affected: N/A.
Why was this product recalled?
Manufacturing defect was found for the cartridge component, which could compromise the sterility barrier of the product
Which agency issued this recall?
This recall was issued by the FDA Devices on July 31, 2019. Severity: Moderate. Recall number: Z-2042-2019.