Device recall
Z-1160-2023: abm Respiratory Care Standart Breating Circuit with Face Mask - Toddler REF…
FDA device recall · Class III · S & MOHR AMERICA, S.A. DE C.V.
Key facts
| Recall number (Z-number) | Z-1160-2023 |
|---|---|
| Recall event | 91562 |
| Product | abm Respiratory Care Standart Breating Circuit with Face Mask - Toddler REF BC21087 abm Respiratory Care Standart Breathing Circuit with Face Mask - Child/Adult Small REF BC21088 abm Respiratory Care Standart Breathing Circuit with Face Mask - Adult Large REF BC21273 abm Respiratory Care Standart… |
| Product code | CAH |
| Recalling firm | S & MOHR AMERICA, S.A. DE C.V. |
| Recall class | Class III |
| Status | Open, Classified |
| 510(k) numbers | K192713 |
| FEI number | 3020777588 |
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