Drug recall
Double Pump RF Patient Cassette; Product Number: 72204055. Intended to provide fluid distension and irrigation…
FDA recall event 74190 · Class II · Medical Vision Ab
Key facts
| Event ID | 74190 |
|---|---|
| Recall numbers | Z-2705-2016 |
| Recalling firm | Medical Vision Ab |
| Product type | Devices |
| Products | Double Pump RF Patient Cassette; Product Number: 72204055. Intended to provide fluid distension and irrigation and fluid suction during diagnostic and operative arthroscopic procedures. |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Sterility of device may be compromised due to sterile package breakage. |
| Initiation date | May 10, 2016 |
| Report date | Sep 7, 2016 |
| Termination date | Sep 18, 2017 |
| City | Nacka |
| Country | Sweden |
| FEI number | 3003647329 |
At a glance
- 1–9 Products in this recall
- 1–9 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: