Device recall
Z-1666-2011: Labeling on box reads: MAQUET BEQ-HG 0284 3/8" X 3/8" Connectors, Lot 70041098…
FDA device recall · Class III · Maquet Cardiovascular, LLC
Key facts
| Recall number (Z-number) | Z-1666-2011 |
|---|---|
| Recall event | 58053 |
| Product | Labeling on box reads: MAQUET BEQ-HG 0284 3/8" X 3/8" Connectors, Lot 70041098 but the product packaged inside was MAQUET BEQ-HG 1113 3/16" x 3/16" Connectors, Lot 70041096. The HG 0284 and HG 1113 connectors are packaged sterile as single components in a container holding 20 units. The connectors… |
| Product code | DWE |
| Recalling firm | Maquet Cardiovascular, LLC |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Sep 13, 2012 |
| 510(k) numbers | K080592 |
| FEI number | 2242352 |
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