Injetak Adjustable Tip Needle
Brand(s)
Last updated
Summary
Product
Injetak Adjustable Tip Needle
Issue
Medical devices - Sterility
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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