International safety notice
Alert 2511 (Technosurveillance) - VR Medical - Illinois sterno-iliac bone marrow aspiration needle Product may not have intact packaging, compromising its stability
Brazil / Anvisa · BRA · Mar 12, 2018
Key facts
| Title | Alert 2511 (Technosurveillance) - VR Medical - Illinois sterno-iliac bone marrow aspiration needle Product may not have intact packaging, compromising its stability |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Trade name: Illinois sternoiliac bone marrow aspiration needle Technical name: Biopsy Needle ANVISA registration number: 80102510723 Risk class: II Affected model: TIN3018 Affected serial number: 841212 |
| Manufacturer | EMPRESA DETENTORA DO REGISTRO VR MEDICAL IMPORTADORA E DISTRIBUIDORA DE PRODUTOS MÉDICOS LTDA CNPJ 04718143000194 RUA BATATAES 391 CONJUNTOS 11 13 R 8ºANDAR SÃO PAULO SP FABRICANTE CAREFUSION 75 NORTH FAIRWAY DRIVE VERNON HILLS IL 60061 ESTADOS UNIDOS TELEFONE 8473629599 FAX 3129499350 EMAIL CLAIREPOLLASKYBDCOM |
| Models | 841212, 80102510723, TIN3018 |
| Date | Mar 12, 2018 |
| 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