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Venni / Biolight
VENNI INSTRUMENTS INC. · Model F80 · UDI-DI 00852503007204
1
510(k) clearances
1,183
Adverse events (195 deaths)
28
Recalls
55
Facilities
Description
Venni / Biolight Fetal Monitor
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2026-05-26 | Philips North America Llc | Monitor has incorrect assembly of the speaker connector which can cause device cables to be pulled out of the housing and increase the risk of intermittent or permanent loss of spe |
| 2026-05-26 | Philips North America Llc | Monitor has incorrect assembly of the speaker connector which can cause device cables to be pulled out of the housing and increase the risk of intermittent or permanent loss of spe |
| 2025-10-24 | Edan Diagnostics | As a result of receiving an FDA It Has Come to Our Attention Letter (IHCTOA Letter) regarding potential cybersecurity issues with various of the firm device. |
| 2025-10-24 | Edan Diagnostics | As a result of receiving an FDA It Has Come to Our Attention Letter (IHCTOA Letter) regarding potential cybersecurity issues with various of the firm device. |
| 2025-10-24 | Edan Diagnostics | As a result of receiving an FDA It Has Come to Our Attention Letter (IHCTOA Letter) regarding potential cybersecurity issues with various of the firm device. |
| 2024-05-22 | Philips North America Llc | Potential for inaccurate fetal heart rate measurements when monitoring multiples. |
| 2019-09-19 | Pacific Medical Group Inc. | Fetal transducers distributed in advance of receiving 510(k) and international clearances. |
| 2019-09-19 | Pacific Medical Group Inc. | Fetal transducers distributed in advance of receiving 510(k) and international clearances. |
| 2019-09-19 | Pacific Medical Group Inc. | Fetal transducers distributed in advance of receiving 510(k) and international clearances. |
| 2019-09-19 | Pacific Medical Group Inc. | Fetal transducers distributed in advance of receiving 510(k) and international clearances. |
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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.