FDAClass IIJuly 31, 2019

Monoject 201 Vet Pak Hypodermic Needle recall: Sterility Concern

Monoject 201 Vet Pak Hypodermic Needle, 22 ga x 1-1/2" Item code: 8881201456

Why was Monoject 201 Vet Pak Hypodermic Needle recalled?

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

What should I do if I have this product?

Review the official FDA enforcement record for current instructions.

What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.

Is my product affected?

Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.

Which lot codes, UPCs or models are affected?

Lot Number: 909117

Product
Monoject 201 Vet Pak Hypodermic Needle, 22 ga x 1-1/2" Item code: 8881201456
Recalling firm
Cardinal Health 200, LLC
Quantity
N/A
Distribution
Nationwide Foreign: AU, BE, CA, DK, FI, GB, IE, NL
Recall date
July 31, 2019
Classification
Class II
Status
Completed
Agency
FDA (device)
Open FDA enforcement record Latest recalls