Device recall
Z-3120-2011: Custom dialysis prep kits labeled as follows: KIDNEYCARE, 125/CS, LOT #A1160…
FDA device recall · Class I · Lee Medical International Inc
Key facts
| Recall number (Z-number) | Z-3120-2011 |
|---|---|
| Recall event | 59692 |
| Product | Custom dialysis prep kits labeled as follows: KIDNEYCARE, 125/CS, LOT #A1160, EXP 7-12, BIN 35A, Lee Medical International, Inc., New Orleans, LA 70123 MESCALERO-HEMO, 200/CS, LOT #B1113, EXP 8-12, Lee Medical International, Inc., New Orleans, LA 70123 DAV-MT-POCONO-H, 200/CS, LOT #B1123, EXP 8-12… |
| Product code | FKG |
| Recalling firm | Lee Medical International Inc |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Jan 30, 2012 |
| FEI number | 2316883 |
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