Covidien
Provision · Model UNVCA12LGF · UDI-DI 00810041638977
NLM
Prescription
1
510(k) clearances
474
Adverse events (1 deaths)
18
Recalls
17
Facilities
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2026-08-19 | Stryker Sustainability Solutions | Reusable access port system may crack or seperate during use. |
| 2026-08-19 | Stryker Sustainability Solutions | Reusable access port system may crack or seperate during use. |
| 2026-08-19 | Stryker Sustainability Solutions | Reusable access port system may crack or seperate during use. |
| 2026-08-19 | Stryker Sustainability Solutions | Reusable access port system may crack or seperate during use. |
| 2026-08-19 | Stryker Sustainability Solutions | Reusable access port system may crack or seperate during use. |
| 2026-08-19 | Stryker Sustainability Solutions | Reusable access port system may crack or seperate during use. |
| 2018-06-19 | Stryker Sustainability Solutions | Through investigation, it was determined that H12LP Trocars in scope of a previous H12LP recall were distributed to facilities within the distribution chain following the recall ex |
| 2016-11-11 | Stryker Sustainability Solutions | An increase in reports indicating that the reprocessed H12LP Trocar adjustable plug may break in the packaging or during use. |
| 2015-07-10 | Stryker Sustainability Solutions | Stryker Sustainability Solutions has received reports indicating that devices from one lot (lot# 3574704) were labeled as 100mm models (CB5LT) while the devices inside of the packa |
| 2015-06-01 | Stryker Sustainability Solutions | Stryker Sustainability Solutions is recalling Trocars because they have received reports indicating that some may fracture at the distal tip resulting in fragments at the surgical |
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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.
