Destino Twist 14F (also branded as Guidestar 14F)
Reported: February 23, 2022 Initiated: December 22, 2021 #Z-0646-2022
Product Description
Destino Twist 14F (also branded as Guidestar 14F)
Reason for Recall
There is potential for separation between the threaded hub and threaded cap at the proximal end of the device.
Details
- Recalling Firm
- Oscor Inc.
- Units Affected
- 549 units
- Distribution
- Distribution to TN and PA in USA OUS distribution to Czech Republic
- Location
- Palm Harbor, FL
Frequently Asked Questions
What product was recalled? ▼
Destino Twist 14F (also branded as Guidestar 14F). Recalled by Oscor Inc.. Units affected: 549 units.
Why was this product recalled? ▼
There is potential for separation between the threaded hub and threaded cap at the proximal end of the device.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on February 23, 2022. Severity: Moderate. Recall number: Z-0646-2022.
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