Device recall
Z-1201-2026: Brand Name: Zimmer Tourniquet Systems Product Name: A.T.S. 5000TS Tourniquet…
FDA device recall · Class II · Zimmer Surgical Inc
Key facts
| Recall number (Z-number) | Z-1201-2026 |
|---|---|
| Recall event | 98235 |
| Product | Brand Name: Zimmer Tourniquet Systems Product Name: A.T.S. 5000TS Tourniquet Systems Model/Catalog Number: 60500010100 Software Version: Software version v2.04 or prior are within scope of the recall for A.T.S. 5000TS Product Description: A.T.S 5000TS Tourniquet Systems Component: N/A |
| Product code | KCY |
| Recalling firm | Zimmer Surgical Inc |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K202919 |
| FEI number | 1526350 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 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