Device recall
Z-0833-2022: (a) CareFusion Snowden-Pencer Plastics, Endoplastic Endoscope 10 mm, 30 degrees…
FDA device recall · Class II · Carefusion 2200 Inc
Key facts
| Recall number (Z-number) | Z-0833-2022 |
|---|---|
| Recall event | 89561 |
| Product | (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 cm, Catalog #88-5920; (c) CareFusion Snowden-Pencer MIS, Endoplastic Fitting, Storz Scope, Catalog… |
| Product code | HET |
| Recalling firm | Carefusion 2200 Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 2, 2023 |
| 510(k) numbers | K982276 |
| FEI number | 3008002452 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 Recalled products with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database