International safety notice
Compresses
Brazil / Anvisa · BRA · Jul 14, 2015
Key facts
| Title | Compresses |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Hérika Sterile Hydrophilic Gauze Surgical Compress/ 11 threads with 10 units 7.5x 7.5cm, registration 80037490012, risk class II, affected batch: 0623. |
| Manufacturer | DETENTOR DO REGISTRO E FABRICANTE AMÉRICA MEDICAL LTDA ENDEREÇO AV SAROBÁ Nº35 MARIA AMÁLIA CURVELOMG BRASIL |
| Models | 80037490012 |
| Date | Jul 14, 2015 |
| 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