International safety notice
Alert 2842 (Technovigilance) Abbott Laboratórios do Brasil Ltda Alinity hq System Instrument Family Possibility of problems related to the product's incubation paddles.
Brazil / Anvisa · BRA · Apr 11, 2019
Key facts
| Title | Alert 2842 (Technovigilance) Abbott Laboratórios do Brasil Ltda Alinity hq System Instrument Family Possibility of problems related to the product's incubation paddles. |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Commercial Name: Alinity hq System Instrument Family Technical Name: Instrument for analyzing or counting cells and platelets ANVISA registration number: 80146502148 Risk Class: II Affected model: Alinity hq Analyzer - Alinity hq Analyzer Affected serial numbers: HQ00231, HQ00232, HQ00235, HQ00236, HQ00237, HQ00238, HQ00239, HQ00240, HQ00275, HQ00280, HQ00301, HQ00304, HQ00305, HQ00308, HQ00 310, HQ00311. |
| Manufacturer | EMPRESA DETENTORA DO REGISTRO ABBOTT LABORATÓRIOS DO BRASIL LTDA CNPJ 56998701000116 RUA MICHIGAN 735 CIDADE MONÇÕES SÃO PAULO SP TEL 55 11 5536 73126 EMAIL CAMILAFERREIRAABBOTTCOM FABRICANTE DO PRODUTO ABBOTT GMBH CO KG ALEMANHA MAXPLANCKRING 2 65205 WIESBADEN ALEMANHA ALEMANHA |
| Models | HQ00236, HQ00304, HQ00308, HQ00240, HQ00231, HQ00310, HQ00237, HQ00275, HQ00238, HQ00239, HQ00280, HQ00311 and 5 more |
| Date | Apr 11, 2019 |
| Regulator page | anvisa.gov.br |
At a glance
- No Recall
- No Field safety notice
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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.
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