6F Taiga Guiding Catheter — Class I medical device recall Z-1207-2018
Terminated recall by Medtronic Inc, reported 2018-04-04. Complaints regarding 6F Taiga guide catheter tip detachment and/or tip splitting.
| Recall number | Z-1207-2018 |
|---|---|
| Product type | Medical device |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Medtronic Inc, Minneapolis, MN, United States |
| Recall initiated | 2017-09-26 |
| Classified | 2018-03-29 |
| Reported by FDA | 2018-04-04 |
| Terminated | 2021-04-27 |
| Countries outside the US | JP |
| Quantity | 15,923 |
| Reason classes | device malfunction |
| Serial numbers | 0008084670, 0008084683, 0008084699, 0008087476, 0008087481, 0008087483, 0008087485, 0008087487, 0008087496, 0008087497, 0008087503, 0008087504, 0008090675, 0008090676, 0008090677, 0008090680, 0008090681, 0008090682, 0008090683, 0008090684, 0008090685, 0008090688, 0008090690, 0008092504, 0008092505 and 475 more |
Product
6F Taiga Guiding Catheter
Reason for recall
Complaints regarding 6F Taiga guide catheter tip detachment and/or tip splitting.
Machine access
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Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.