Device recall
Z-1772-2021: MiniMed 670G Insulin Pump: Models: PUMP MMT-1740KX 670G V6.3 SF MG CLIN; PUMP…
FDA device recall · Class II · Medtronic Minimed
Key facts
| Recall number (Z-number) | Z-1772-2021 |
|---|---|
| Recall event | 87735 |
| Product | MiniMed 670G Insulin Pump: Models: PUMP MMT-1740KX 670G V6.3 SF MG CLIN; PUMP MMT-1740KX 670G V6.3 CLIN 020 MG; PUMP MMT-1741KFX 670G V6.3 SF MG CLIN FR; PUMP MMT-1741KFX 670G V6.3 CLIN 020 MG; PUMP MMT-1741KX 670G V6.3 SF MG CLIN GER; PUMP MMT-1741KX 670G V6.3 CLIN 020 MG; PUMP MMT-1741KXS 670G… |
| Product code | OZP |
| Recalling firm | Medtronic Minimed |
| Recall class | Class II |
| Status | Open, Classified |
| FEI number | 3003166194 |
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