6F Taiga Guiding Catheter
Reported: April 4, 2018 Initiated: September 26, 2017 #Z-1207-2018
Product Description
6F Taiga Guiding Catheter
Reason for Recall
Complaints regarding 6F Taiga guide catheter tip detachment and/or tip splitting.
Details
- Recalling Firm
- Medtronic Inc
- Units Affected
- 15,923
- Distribution
- Japan
- Location
- Minneapolis, MN
Frequently Asked Questions
What product was recalled? ▼
6F Taiga Guiding Catheter. Recalled by Medtronic Inc. Units affected: 15,923.
Why was this product recalled? ▼
Complaints regarding 6F Taiga guide catheter tip detachment and/or tip splitting.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on April 4, 2018. Severity: Critical. Recall number: Z-1207-2018.
Related Recalls
FDA Devices Moderate
Convenience Kits 1. 25GA Convenience Kit - FNX VS0644.25-FNX 2. 25GA Convenience Kit - FXX VS0644.25-FXX 3.2…
Vortex Surgical Inc. · 2026-02-11
FDA Devices Moderate
COULTER DxH Diluent, REF 628017 COULTER DxH ECO Diluent REF C67250 For use as an isotonic buffered diluent in conju…
Beckman Coulter, Inc. · 2026-02-11
FDA Devices Moderate
Product Name: Single Use 3-Lumen Sphincterotome V Model/Catalog Number: KD-V411M-1520 Product Description: These inst…
Olympus Corporation of the Americas · 2026-02-11
FDA Devices Moderate
Product Name: Disposable Triple Lumen Sphincterotome Model/Catalog Number: KD-401Q-0330 Product Description: These in…
Olympus Corporation of the Americas · 2026-02-11
FDA Devices Moderate
Product Name: Lumipulse pTau 217 Plasma Controls Model/Catalog Number: 81558 Software Version: Not Applicable Produc…
Fujirebio Diagnostics, Inc. · 2026-02-11