International safety notice
IMPLANT
Brazil / Anvisa · BRA · Feb 15, 2012
Key facts
| Title | IMPLANT |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | LUPINE LOOP ANCHOR SYSTEM WITH ORTHOCORD - Registration 80145900903 - Affected lots: all numbers below 3571653 of lupine product codes: 201704, 210705, 210707, 210708, 210709, 210710, 210711, 210712, 222980 and 222981. |
| Manufacturer | DETENTOR DO REGISTRO DO PRODUTO NO BRASIL JOHNSON JOHNSON DO BRASIL IND E COM DE PROD PARA SAÚDE LTDA RUA GERIVATIBA NO 207 BUTANTÂ SÃO PAULOSP FONEFAX 012 39321659012 39321963 |
| Models | 222981, 210709, 222980, 210708, 3571653, 210711, 210707, 210712, 80145900903, 201704, 210710, 210705 |
| Date | Feb 15, 2012 |
| Regulator page | anvisa.gov.br |
At a glance
- No Recall
- No Field safety notice
- 1–9 Matching device models in FDA data
- 1–9 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