Durepair Dura Subsitute
Brand(s)
Last updated
Summary
Product
Durepair Dura Subsitute
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 catalogue number |
|---|---|---|
Durepair Dura Subsitute |
More than 10 numbers, contact manufacturer. |
61110 |
Issue
Medtronic was informed by the contract manufacturer that based on internal investigation they have identified issues with in-process and finished goods endotoxin testing. these issues may have resulted in the release of product with out-of-specification endotoxin levels.
Recall start date: June 13, 2023
Additional information
Details
Original published date:
Alert / recall type
Health product recall
Category
Health products - Medical devices - Neurology
Companies
| Medtronic Inc. |
| 710 Medtronic Parkway N.E., Minneapolis, Minnesota, United States, 55432 |
Published by
Health Canada
Audience
Healthcare
Recall class
Type II
Identification number
RA-73891
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