Device recall
Z-0753-2021: Smoothbore breathing system with exhalation port 22 mm Device REF #: B0062001…
FDA device recall · Class II · Intersurgical Inc
Key facts
| Recall number (Z-number) | Z-0753-2021 |
|---|---|
| Recall event | 86800 |
| Product | Smoothbore breathing system with exhalation port 22 mm Device REF #: B0062001 Custom Anasthesia Breathing Systems; Multipac Anasthesia Breathing Systems - Product Usage: intended to administer medical gases to a patient during anesthesia. It provides both an inhalation and exhalation route and may… |
| Product code | OFP |
| Recalling firm | Intersurgical Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 9, 2022 |
| FEI number | 1000120301 |
At a glance
- None 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