Device recall
Z-1331-04: Greiner bio-one, VACUETTE TUBE, 9NC Coagulation Citrate 3.2%, 3.5ml blue…
FDA device recall · Class II · Greiner VACUETTE North America
Key facts
| Recall number (Z-number) | Z-1331-04 |
|---|---|
| Recall event | 29652 |
| Product | Greiner bio-one, VACUETTE TUBE, 9NC Coagulation Citrate 3.2%, 3.5ml blue cap-black ring, 24 racks of 50, 1200 pcs in total, non ridged, sandwich tube, Ref: 454332, Lot B040404, Expiry 2005-04, Sterile. |
| Product code | GIM |
| Recalling firm | Greiner VACUETTE North America |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 29, 2004 |
| 510(k) numbers | K971221 |
| FEI number | 3001451379 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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