Health product recall

Injetak Adjustable Tip Needle

Last updated

Summary

Product
Injetak Adjustable Tip Needle
Issue
Medical devices - Sterility Issue
What to do

Contact the manufacturer if you require additional information. 

Audience
Healthcare

Affected products

Affected products

Lot or serial number

Model or catalog number

Injetak Adjustable Tip Needle

More than 10 numbers, contact manufacturer.

DIS201

Injetak Adjustable Tip Needle

More than 10 numbers, contact manufacturer.

DIS199

Issue

Laborie became aware of the damaged packaging through the complaint process. A complaint case was issued in response to a customer complaint involving a small hole found in the film of the sterile barrier of the Injetak needle packaging (dis201). Further investigation demonstrated that the issue was also present in product inventory (dis199).

Recall start date: February 07, 2023

Additional information

Details
Original published date:
Alert / recall type
Health product recall
Category
Health products - Medical devices - General hospital and personal use
Companies

Laborie Medical Technologies, Corp.

180 International Dr., Portsmouth, New Hampshire, United States, 03801

Published by
Health Canada
Audience
Healthcare
Recall class
Type II
Identification number
RA-73117

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