Device recall
Z-0178-2020: Minimed Model 503 Remote Transmitter (MMT-503, MMT-503EU, MMT-503NA, MMT-503US)…
FDA device recall · Class I · Medtronic Inc.
Key facts
| Recall number (Z-number) | Z-0178-2020 |
|---|---|
| Recall event | 82078 |
| Product | Minimed Model 503 Remote Transmitter (MMT-503, MMT-503EU, MMT-503NA, MMT-503US) for use with the MiniMed Paradigm Insulin Pump (MMT-523/723, MMT-523K/723K, MMT-551/751, MMT-554/754, MMT-522/722, MMT-522K/722K, MMT-515/715, MMT-512/712, MMT-511) |
| Product code | LZG |
| Recalling firm | Medtronic Inc. |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Mar 29, 2024 |
| 510(k) numbers | K001829, K120206 |
| FEI number | 3003166194 |
At a glance
- 1–9 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