Device recall
Z-1802-2022: Medical Monofilament Manufacturing MONOFILIMENT TEST, SENSORY F/FOOT 10GM…
FDA device recall · Class III · Mckesson Medical-Surgical Inc. Corporate Office
Key facts
| Recall number (Z-number) | Z-1802-2022 |
|---|---|
| Recall event | 90731 |
| Product | Medical Monofilament Manufacturing MONOFILIMENT TEST, SENSORY F/FOOT 10GM (40/PK) Model Number: AM140 |
| Product code | GAQ |
| Recalling firm | Mckesson Medical-Surgical Inc. Corporate Office |
| Recall class | Class III |
| Status | Open, Classified |
| FEI number | 3004386693 |
At a glance
- None Linked 510(k)s
- 10–99 Products in the same recall event
- 1–9 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