Device recall
Z-0368-05: McKesson Medi-Pak Elastic Bandages, Premium, Sterile; rolled elastic bandage…
FDA device recall · Class III · Cypress Medical Products, Ltd.
Key facts
| Recall number (Z-number) | Z-0368-05 |
|---|---|
| Recall event | 30550 |
| Product | McKesson Medi-Pak Elastic Bandages, Premium, Sterile; rolled elastic bandage, single patient use, knit, single self closure, latex-free; Marketed by McKesson Corporation, McKesson Medical-Surgical, Richmond, VA 23228, Made in Canada, Packaged, sterilized and inspected in the U.S.A.; the elastic… |
| Product code | FQM |
| Recalling firm | Cypress Medical Products, Ltd. |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Sep 21, 2005 |
| FEI number | 1451040 |
At a glance
- None 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