International safety notice
Alert 2502 (Technovigilance) - Medtronic - Minimed 640G Insulin Pump Device buttons may become difficult to press or unresponsive to the touch.
Brazil / Anvisa · BRA · Feb 28, 2018
Key facts
| Title | Alert 2502 (Technovigilance) - Medtronic - Minimed 640G Insulin Pump Device buttons may become difficult to press or unresponsive to the touch. |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Trade name: Minimed 640G Insulin Pump Technical name: Infusion Pump ANVISA registration number: 10339190656 Risk class: III Modelo afetado: MMT-1712K; MMT-1752; MMT-1752K; MMT-1752KBP; MMT-1752WWK; MMT-1752WWKA Affected serial number: See distribution map |
| Manufacturer | EMPRESA DETENTORA DO REGISTRO MEDTRONIC COMERCIAL LTDA CNPJ 01772798000152 AV JORNALISTA ROBERTO MARINHO 85 10º ANDAR CEP 04675010 SÃO PAULO SP FABRICANTE MEDTRONIC PUERTO RICO OPERATIONS CO JUNCOS ROAD 31 KM 24 HM 4 CEIBA NORTE INDUSTRIAL PARK JUNCOS PR 00777PORTO RICO |
| Models | MMT-1752, MMT-1712K, MMT-1752K, MMT-1752KBP, MMT-1752WWK, MMT-1752WWKA, 10339190656 |
| Date | Feb 28, 2018 |
| Regulator page | anvisa.gov.br |
At a glance
- No Recall
- No Field safety notice
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About International device safety notices
Field safety notices, recalls and safety alerts published by about 30 national medical device regulators outside the United States, matched by Orca1 to FDA device data.
Source: National medical device regulators (as listed), compiled by Orca1