Home › RESEARCH INSTRUMENTS LIMITED › G185
G185
RESEARCH INSTRUMENTS LIMITED · Model K22400-110 G185 Standard 110V Incubator ROW · UDI-DI 05060554120086
1
510(k) clearances
5
Adverse events
6
Recalls
21
Facilities
Description
G185 Incubator for assisted reproduction
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2024-11-15 | CooperSurgical, Inc. | The warming surfaces or incubator well temperatures of the listed products may exceed the desired set temperature. If temperatures exceed the desired set value, the device will al |
| 2024-11-15 | CooperSurgical, Inc. | The warming surfaces or incubator well temperatures of the listed products may exceed the desired set temperature. If temperatures exceed the desired set value, the device will al |
| 2024-11-15 | CooperSurgical, Inc. | The warming surfaces or incubator well temperatures of the listed products may exceed the desired set temperature. If temperatures exceed the desired set value, the device will al |
| 2024-11-15 | CooperSurgical, Inc. | The warming surfaces or incubator well temperatures of the listed products may exceed the desired set temperature. If temperatures exceed the desired set value, the device will al |
| 2024-11-15 | CooperSurgical, Inc. | The warming surfaces or incubator well temperatures of the listed products may exceed the desired set temperature. If temperatures exceed the desired set value, the device will al |
| 2024-11-15 | CooperSurgical, Inc. | The warming surfaces or incubator well temperatures of the listed products may exceed the desired set temperature. If temperatures exceed the desired set value, the device will al |
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.