Device recall
Z-1136-03: 75-1650 Drip Chambers.138rr; Abbott, Ashland, Ohio 44805; 800 drip chambers per…
FDA device recall · Class II · Abbott Laboratories HPD/ADD
Key facts
| Recall number (Z-number) | Z-1136-03 |
|---|---|
| Recall event | 26450 |
| Product | 75-1650 Drip Chambers .138rr; Abbott, Ashland, Ohio 44805; 800 drip chambers per case; Abbott Commodity 751650, Ashland Product #85-16500 |
| Product code | FPA |
| Recalling firm | Abbott Laboratories HPD/ADD |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 27, 2004 |
| FEI number | 1415939 |
At a glance
- None Linked 510(k)s
- 10–99 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