International safety notice
Alert 2867 (Technovigilance) - Stryker do Brasil LTDA - Pneumosure Heated RTP Inflator Tube - Pneumosure Inflator Tube Probability that the inflation tube will disconnect from the cassette.
Brazil / Anvisa · BRA · May 3, 2019
Key facts
| Title | Alert 2867 (Technovigilance) - Stryker do Brasil LTDA - Pneumosure Heated RTP Inflator Tube - Pneumosure Inflator Tube Probability that the inflation tube will disconnect from the cassette. |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Commercial Name: Pneumosure Heated RTP Inflator Tube; Technical Name: Equipment ANVISA registration number: 80005430169 Risk Class: II Affected model: 0620040690; Affected batch numbers: Model 0620040690: 56004575; |
| Manufacturer | EMPRESA DETENTORA DO REGISTRO STRYKER DO BRASIL LTDA CNPJ 02966317000102 RUA URUSSUÍ 300 8º ANDAR SÃO PAULO SP TEL 11 51892550 EMAIL QUALIDADESTRYKERCOM FABRICANTE DO PRODUTO STRYKER CORPORATION ESTADOS UNIDOS DA AMÉRICA |
| Models | 80005430169, 0620040690, 56005433, 56004575, 56005297, 56005177, 56005397, 0620040660, 56005075, 56004723, 56005085, 56006432 |
| Date | May 3, 2019 |
| 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