Nobel Biocare® 37470Recalls & reported problems
Nobel Biocare AB · Implant Retrieval Kit · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 0
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 1
Summary
No MAUDE adverse event reports in our data reference this device identifier directly.
1 FDA recall record name this device's identifier.
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Recalls naming this device
- Mar 14, 2019Class IITerminated
Due to a problem in the packaging sealing process at the supplier of the affected devices, it cannot be guaranteed that the sterilized medical devices in the scope of this recall remain sterile during their shelf-life.
Z-1323-2020 · Root cause: Packaging process control · Recall details · FDA record ↗
Other DRILL, BONE, POWERED devices
- NA 03.505.004Synthes GmbH · DRILL, BONE, POWERED69 reports
- MatrixMANDIBLE 03.503.476Synthes GmbH · DRILL, BONE, POWERED26 reports
- NA 310.510Synthes GmbH · DRILL, BONE, POWERED17 reports
- NA 317.82Synthes GmbH · DRILL, BONE, POWERED16 reports
- MatrixMANDIBLE 03.503.479Synthes GmbH · DRILL, BONE, POWERED11 reports
- NA 05.001.120Synthes GmbH · DRILL, BONE, POWERED9 reports
- NA 310.520Synthes GmbH · DRILL, BONE, POWERED9 reports
- NA 03.505.006Synthes GmbH · DRILL, BONE, POWERED8 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026 · each recall links to the FDA recall notice
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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