Drug recall
Stryker, REF PC9001, PINPOINT Video Processor/Illuminator, Rx Only CE 0197, MD Medical Device, UDI: (01)…
FDA recall event 87540 · Class II · Stryker Corporation
Key facts
| Event ID | 87540 |
|---|---|
| Recall numbers | Z-1428-2021 |
| Recalling firm | Stryker Corporation |
| Product type | Devices |
| Products | Stryker, REF PC9001, PINPOINT Video Processor/Illuminator, Rx Only CE 0197, MD Medical Device, UDI: (01) 00858701006049 - Product Usage: used with both the SPY-PHI and PINPOINT systems, the intended… |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Their is a potential that Video Processor/Illuminators may exhibit flickering, loss of image or unintended reboots. |
| Initiation date | Feb 26, 2021 |
| Report date | Apr 21, 2021 |
| Termination date | Dec 15, 2023 |
| City | San Jose |
| State | CA |
| Country | United States |
| FEI number | 2936485 |
At a glance
- 1–9 Products in this recall
- 10–99 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: