Device recall
Z-0129-06: Bari Maxx II, KCI''s BariMaxx II bariatric bed, P/N 310611, November 2001, KCI…
FDA device recall · Class II · Kinetic Concepts, Inc
Key facts
| Recall number (Z-number) | Z-0129-06 |
|---|---|
| Recall event | 33679 |
| Product | Bari Maxx II, KCI''s BariMaxx II bariatric bed, P/N 310611, November 2001, KCI The Clinical Advantage, P. O. Box 659508, San Antonio, Texas 78265-9508, Call Toll Free 1-800-531-5346, FAX (210) 308-3998, Http://www.kci1.com |
| Product code | FNL |
| Recalling firm | Kinetic Concepts, Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Nov 8, 2005 |
| FEI number | 1625774 |
At a glance
- None Linked 510(k)s
- 1–9 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