Device recall
Z-2621-2026: A M S, ALIGNED MEDICAL SOLUTIONS, Preop Kit-NS, Pack Number AMS18227, surgical…
FDA device recall · Class I · Windstone Medical Packaging, Inc.
Key facts
| Recall number (Z-number) | Z-2621-2026 |
|---|---|
| Recall event | 99189 |
| Product | A M S, ALIGNED MEDICAL SOLUTIONS, Preop Kit-NS, Pack Number AMS18227, surgical convenience kit |
| Product code | LRO |
| Recalling firm | Windstone Medical Packaging, Inc. |
| Recall class | Class I |
| Status | Open, Classified |
| FEI number | 1000125955 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 1,000+ 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