Medtronic Navigation, Inc.-Littleton: 5 recalls on record
Recalls filed with 1 agency: FDA (5).
First recall on record: October 19, 2016. Most recent: June 12, 2024.
Risk classification: Class II: 5
Most recent recalls
| Date | Agency | Product | Recall number |
|---|---|---|---|
| June 12, 2024 | FDA | O-arm O2 Imaging System-Mobile x-ray system designed for 2D fluoroscopic and 3D imaging f…Z-2026-2024 | Z-2026-2024 |
| July 10, 2019 | FDA | Medtronic 0-arm TM 1000 Imaging Systems: Bl-700-00027-XXX and B1-700-00028-XXX (where XXX…Z-1932-2019 | Z-1932-2019 |
| October 31, 2018 | FDA | O-arm 1000 2nd Edition Imaging System, OARM ASSY Bl70000027 SYSTEM PRODUCT, Model Number …Z-0271-2019 | Z-0271-2019 |
| October 31, 2018 | FDA | O-arm 1000 2nd Edition Imaging System, OARM ASSY Bl70000027R SYS PRODUCT RWK, Model Numbe…Z-0272-2019 | Z-0272-2019 |
| October 19, 2016 | FDA | Medtronic Navigation O-arm O2 Surgical Imaging System Product Catalog Number: BI-700-0200…Z-0070-2017 | Z-0070-2017 |
Questions about this company
- How many recalls does Medtronic Navigation, Inc.-Littleton have?
- Recalert has 5 U.S. recalls on record for Medtronic Navigation, Inc.-Littleton, published between October 19, 2016 and June 12, 2024.
- What was the most recent Medtronic Navigation, Inc.-Littleton recall?
- FDA recall Z-2026-2024, published June 12, 2024: O-arm O2 Imaging System-Mobile x-ray system designed for 2D fluoroscopic and 3D imaging for adult and pediatric patients. Product Number: BI70002000
- Which agencies have handled Medtronic Navigation, Inc.-Littleton recalls?
- Medtronic Navigation, Inc.-Littleton appears as the recalling firm in recalls from: FDA (5).
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