Drug recall
(a) CareFusion Snowden-Pencer Plastics, Endoplastic Endoscope 10 mm, 30 degrees 7", 17.5 cm, Catalog #88-5910…
FDA recall event 89561 · Class II · Carefusion 2200 Inc
Key facts
| Event ID | 89561 |
|---|---|
| Recall numbers | Z-0833-2022 |
| Recalling firm | Carefusion 2200 Inc |
| Product type | Devices |
| Products | (a) CareFusion Snowden-Pencer Plastics, Endoplastic Endoscope 10 mm, 30 degrees 7", 17.5 cm, Catalog #88-5910; (b) CareFusion Snowden-Pencer Plastics, Endoplastic Endoscope 5 mm, 30 degrees 7", 17.5… |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | The finished device package did not contain the IFU. |
| Initiation date | Feb 23, 2022 |
| Report date | Apr 6, 2022 |
| Termination date | May 2, 2023 |
| City | Vernon Hills |
| State | IL |
| Country | United States |
| FEI number | 3008002452 |
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: