Home › SIMAVITA (AUST) PTY LTD › SIM assess sensor pad kit - MODERATE
SIM assess sensor pad kit - MODERATE
SIMAVITA (AUST) PTY LTD · Model 6022 · UDI-DI 09342124000452
1
510(k) clearances
965
Adverse events (1 deaths)
4
Recalls
19
Facilities
Description
SIM assess sensor pad MODERATE kit which contains: - 20 x SIM assess sensor pad MODERATE - 9 x SIM pants REGULAR
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2022-09-30 | Baxter Healthcare Corporation | Radio frequency emission from a functioning WatchCare device may potentially impact other devices (including, but not limited to telemetry devices, bladder scanner, fetal monitor/d |
| 2022-09-30 | Baxter Healthcare Corporation | Radio frequency emission from a functioning WatchCare device may potentially impact other devices (including, but not limited to telemetry devices, bladder scanner, fetal monitor/d |
| 2022-09-30 | Baxter Healthcare Corporation | Radio frequency emission from a functioning WatchCare device may potentially impact other devices (including, but not limited to telemetry devices, bladder scanner, fetal monitor/d |
| 2022-09-30 | Baxter Healthcare Corporation | Radio frequency emission from a functioning WatchCare device may potentially impact other devices (including, but not limited to telemetry devices, bladder scanner, fetal monitor/d |
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.