International safety notice
EXTENSOR
Brazil / Anvisa · BRA · Mar 5, 2012
Key facts
| Title | EXTENSOR |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | CONNECTOR TUBE - Registration 80136710118 Presentation in Y 60" CODE 801106 - Affected Lots: 0022187; 0029497; 0064349; 0067042; 0288027; 0344214; 9135201; 9163184; 9191016; 9240130; 92470 97. Presentation in Y 90" CODE 801107 - Affected Lots: 0029498; 0032077; 0081113; 0148235; 0225223; 0253258; 0273019; 0295181; 1014141; 1021230; 10282 27; 1042218; 1042219; 1056020; 1070126; 1091205; 1098205; 1112018; 1196145; 9058254; 9058255; 9086222; 9170276; 9191018; 9345196; 9191019; 9212121; 9275100; 9295023; 9320079; 9327016; 9334064. Presentation 60BP CODE. |
| Manufacturer | DETENTOR DO REGISTRO NO BRASIL MALLINCKRODT DO BRASIL LTDA AV DAS NAÇÕES UNIDAS 23130 SÃO PAULOSP FONEFAX 11218762731121876225 |
| Models | 0344201, 9212121, 0043273, 1070126, 0273019, 9320072, 0127197, 80136710118, 0295171, 1021226, 9357266, 1112018 and 82 more |
| Date | Mar 5, 2012 |
| Regulator page | anvisa.gov.br |
At a glance
- No Recall
- No Field safety notice
- 10–99 Matching device models in FDA data
- 10–99 Matching catalog numbers in FDA data
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