VirtuTRAX Instrument Navigator, 10 17 GA VirtuTRAX
Reported: December 29, 2021 Initiated: October 8, 2021 #Z-0398-2022
Product Description
VirtuTRAX Instrument Navigator, 10 17 GA VirtuTRAX
Reason for Recall
There is potential that the VirtuTRAX device will not tighten onto the instrument to be used.
Details
- Recalling Firm
- Civco Medical Instruments Co. Inc.
- Units Affected
- 599 boxes (5 units/box)
- Distribution
- Worldwide distribution - US Nationwide and the countries of Belgium, Canada, China (Mainland), China (Taiwan), Denmark, France, Germany, Italy, Japan, Netherlands, Singapore, South Korea, Spain, Thailand.
- Location
- Kalona, IA
Frequently Asked Questions
What product was recalled? ▼
VirtuTRAX Instrument Navigator, 10 17 GA VirtuTRAX. Recalled by Civco Medical Instruments Co. Inc.. Units affected: 599 boxes (5 units/box).
Why was this product recalled? ▼
There is potential that the VirtuTRAX device will not tighten onto the instrument to be used.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on December 29, 2021. Severity: Moderate. Recall number: Z-0398-2022.
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