Device recall
Z-0491-2012: McKESSON Medi-Pak Urethral Catheter Tray with Red Rubber Catheter Sterile.Single…
FDA device recall · Class II · Nurse Assist, Inc
Key facts
| Recall number (Z-number) | Z-0491-2012 |
|---|---|
| Recall event | 60412 |
| Product | McKESSON Medi-Pak Urethral Catheter Tray with Red Rubber Catheter Sterile.Single Use.Disposable 20 Trays Per Case Reorder No. 37-232 CAUTION: THIS PRODUCT CONTAINS NATURAL RUBBER LATEX WHICH MAY CAUSE ALLERGIC REACTIONS Marketed by McKesson Corporation McKesson Medical-Surgical, Richmond, VA 23228… |
| Product code | KOD |
| Recalling firm | Nurse Assist, Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 26, 2012 |
| 510(k) numbers | K830359 |
| FEI number | 3002695476 |
At a glance
- 1–9 Linked 510(k)s
- 10–99 Products in the same recall event
- 100–999 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