Device recall
Z-0051-04: propper brand cal-mark(R), Micro-Hematocrit Calibrated Capillary Tubes…
FDA device recall · Class II · Propper Mfg Co Inc
Key facts
| Recall number (Z-number) | Z-0051-04 |
|---|---|
| Recall event | 26844 |
| Product | propper brand cal-mark(R), Micro-Hematocrit Calibrated Capillary Tubes, CALIBRATED-HEPARINIZED, reorder no. 043021, 6 Vials, 100 Tubes per Vial, Length 75 mm., 0.55 mm. I.D., 1.40-1.75mm. O.D. Calibrated 60mm from end for use in direct reading centrifuges. Fill to the 60mm mark with blood and seal… |
| Product code | G-IO |
| Recalling firm | Propper Mfg Co Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 23, 2003 |
| FEI number | 2410251 |
At a glance
- None 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