International safety notice
Alert 2582 (Technovigilance) - Becton Dickinson Indústrias Cirúrgicas Ltda - BD Posiflush Heparin Lock Flush Syringe Recall of syringes with heparin due to suspected contamination of the material.
Brazil / Anvisa · BRA · Jun 4, 2018
Key facts
| Title | Alert 2582 (Technovigilance) - Becton Dickinson Indústrias Cirúrgicas Ltda - BD Posiflush Heparin Lock Flush Syringe Recall of syringes with heparin due to suspected contamination of the material. |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Product or case identification: Nome Comercial: BD Posiflush Heparin Lock Flush Syringe Technical Name: Disposable Syringes ANVISA registration number: 10033430366 Risk Class: IV Affected model: BD Posiflush Syringe with Heparin, USP, 300 units/3mL (100 units/mL) 3mL in 10mL syringe Affected serial numbers: Lot No.: 708782N and 709772N. |
| Manufacturer | EMPRESA DETENTORA DO REGISTRO BECTON DICKINSON INDÚSTRIAS CIRÚRGICAS LTDA CNPJ 21551379000106 AVENIDA PRESIDENTE JUSCELINO KUBITSCHEK 273 JUIZ DE FORA MG TEL 11 5185 9990 EMAIL BRCRBDCOM FABRICANTE DO PRODUTO BECTON DICKINSON AND COMPANY 1 BECTON DRIVE FRANKLIN LAKES NJ 07417 EUA |
| Models | 709772N, 708782N, 10033430366 |
| Date | Jun 4, 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