Device recall
Z-1981-2026: Convenience kits containing Medline Namic Angiographic Control Syringes with…
FDA device recall · Class I · American Contract Systems Inc
Key facts
| Recall number (Z-number) | Z-1981-2026 |
|---|---|
| Recall event | 98720 |
| Product | Convenience kits containing Medline Namic Angiographic Control Syringes with Rotating Adaptor CORONARY ANGIO PACK Model numbers ANCA80AP ANCA80AQ |
| Product code | LRO |
| Recalling firm | American Contract Systems Inc |
| Recall class | Class I |
| Status | Open, Classified |
| FEI number | 3008492337 |
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