Device recall
Z-1100-04: STERIS Kindest Kare Perineal Cleanser Incontinence System, packaged in 4-fl. oz…
FDA device recall · Class III · Steris Corportion
Key facts
| Recall number (Z-number) | Z-1100-04 |
|---|---|
| Recall event | 29263 |
| Product | STERIS Kindest Kare Perineal Cleanser Incontinence System, packaged in 4-fl. oz. bottles (72 per case), Ready-To-Use, No-Rinse Solution, For Pediatric and Geriatric Use, For Hospital and Professional Use Only. The label shows the responsible firm to be STERIS Corporation, St. Louis, MO. |
| Product code | JD-01 |
| Recalling firm | Steris Corportion |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Nov 15, 2004 |
| FEI number | 1937531 |
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