Home › Nordicneurolab AS › BatteryCharger
BatteryCharger
Nordicneurolab AS · Model 1.0 · UDI-DI 07090042053075
1
510(k) clearances
4,751
Adverse events (37 deaths)
711
Recalls
145
Facilities
Description
nordicAudio is an audio system for use in MR. The BatteryCharger is a charger for the MR compatible BatteryBox. The Charger itself is MR unsafe.
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2026-08-21 | Philips North America Llc | A software issue will terminate an examination during the image reconstruction process if the scan parameters are manually adjusted such that reconstruction requirements exceed the |
| 2026-08-21 | Philips North America Llc | A software issue will terminate an examination during the image reconstruction process if the scan parameters are manually adjusted such that reconstruction requirements exceed the |
| 2026-08-21 | Philips North America Llc | A software issue will terminate an examination during the image reconstruction process if the scan parameters are manually adjusted such that reconstruction requirements exceed the |
| 2026-08-21 | Philips North America Llc | A software issue will terminate an examination during the image reconstruction process if the scan parameters are manually adjusted such that reconstruction requirements exceed the |
| 2026-08-21 | Philips North America Llc | A software issue will terminate an examination during the image reconstruction process if the scan parameters are manually adjusted such that reconstruction requirements exceed the |
| 2026-08-21 | Philips North America Llc | A software issue will terminate an examination during the image reconstruction process if the scan parameters are manually adjusted such that reconstruction requirements exceed the |
| 2026-08-21 | Philips North America Llc | A software issue will terminate an examination during the image reconstruction process if the scan parameters are manually adjusted such that reconstruction requirements exceed the |
| 2026-08-21 | Philips North America Llc | A software issue will terminate an examination during the image reconstruction process if the scan parameters are manually adjusted such that reconstruction requirements exceed the |
| 2026-08-21 | Philips North America Llc | A software issue will terminate an examination during the image reconstruction process if the scan parameters are manually adjusted such that reconstruction requirements exceed the |
| 2026-08-21 | Philips North America Llc | A software issue will terminate an examination during the image reconstruction process if the scan parameters are manually adjusted such that reconstruction requirements exceed the |
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
Get your free API keyRead the docsData compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.