Device recall
Z-2640-2023: 3M Attest Super Rapid 5 Steam-Plus Steam Challenge Pack, REF 41482VF; designed…
FDA device recall · Class II · 3M Company - Health Care Business
Key facts
| Recall number (Z-number) | Z-2640-2023 |
|---|---|
| Recall event | 92915 |
| Product | 3M Attest Super Rapid 5 Steam-Plus Steam Challenge Pack, REF 41482VF; designed to qualify and monitor dynamic-air removal steam sterilization processes |
| Product code | FRC |
| Recalling firm | 3M Company - Health Care Business |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K193154 |
| FEI number | 2110898 |
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