Criar um relatório

Forneça o título do relatório
Forneça a localização
Forneça detalhes

Adicionar mais

Receba alertas e atualizações para seu caso!

Esta informação não é mostrada no site. Podemos notificá-lo sobre atualizações e podemos entrar em contato com você para obter mais informações para ajudar a resolver ou acompanhar seu problema.

Forneça e-mail ou telefone
Forneça e-mail ou telefone

Não mostramos seu e-mail ou informações de contato

Ignore esta etapa

Adicionar fotos ou vídeos

Recomendamos fotos e vídeos para ajudar a explicar seu relatório

Adicionar foto/vídeo
Solte arquivos aqui
Ignorar esta etapa

Cópia do relatório por e-mail ou SMS

Digite abaixo para receber uma cópia do seu relatório por e-mail ou envie um link para o seu relatório.

Forneça e-mail ou telefone
Forneça e-mail ou telefone

Obrigado pelo seu relatório!

IMPORTANTE - Seu relatório está na fila Pode levar até 12 horas para que seu relatório seja exibido em nossa página inicial (se não for optado como privado)


O relatório foi enviado com sucesso!



Seu relatório está na fila. Pode levar até 12 horas para ser processado.


Envie-nos um e-mail para support@safelyhq.com se você tiver dúvidas.

Recall notice

Universal Meditech Inc. Atualização de kits de teste - recolhidos devido à Segurança do Produto/Defeito, USA

há 2 anos source fda.gov

United States

On May 22, 2023, Universal Meditech Inc. initiated a nationwide recall of products it manufactured between March 2021 and November 2022. The recall is due to the reasons that: The company is going out of business, hence would not be able to continue fulfilling any post-market responsibilities of these distributed products. 4 of the products (PrestiBio Breastmilk Alcohol Test Strip, PrestiBio™ Ketone Test Strips, HealthyWiser KetoFast™ Ketone Test Strips and DiagnosUS® SARS-CoV-2 Antibody (IgG/IgM) Test) have been violatively distributed without appropriate premarket clearance or approval which potentially could result in inaccurate test results due to lack of performance evaluation by the FDA. These products have been distributed to distributors in California, New York, New Jersey, and Florida, and they may have been further sold to end consumers national-wide across the United States. To date, there has not been any reported injury due to the use of any of the products.

Recalled products were manufactured and distributed from March 2021 to November 2022. The following styles/models/UDI have been recalled:

No. Product Name UDI Number Lot Number to be Recalled
1 One Step® Pregnancy Test B512100011 3-H25052-20UMI 3-H07102-20UMI
2 One Step® Ovulation Test* B512200011 3-L12121-20UMI 3-L07102-20UMI
3 HealthyWiser UriTest™ 10 Parameter Reagent Test Strips for Urinalysis None** URS-1-2104-01 URS-1-2102-02 URS-1-2105-01 URS-1-2106-02 URS-1-2110-02
4 HealthyWiser UriTest™ UTI Test Strips None** URS-1-2102-03 URS-1-2106-01 URS-1-2202-01-Q URS-1-2204-01 URS-1-2207-01 URS-1-2209-01
5 HealthyWiser KetoFast™ Ketone Test Strips None** URS-1-2104-02
6 HealthyWiser pH-Aware™ pH Test Strips None** URS-1-2105-01-Q URS-1-2105-02-Q URS-1-2108-01-Q URS-1-2109-01-Q URS-1-2111-01-Q
7 hCG Pregnancy Cassette None** hCG-M5-2101-01 hCG-M5-2104-01 hCG-M5-2106-01 hCG-M5-2107-01 hCG-M5-2108-01 hCG-M5-2110-01 hCG-M5-2202-01 hCG-M5-2202-02hCG-M5- 2202-03 hCG-M5-2203-01 hCG-M5-2204-01 hCG-M5-2204-02 hCG-M5-2204-03 hCG-M5-2206-01 hCG-M5-2206-02 hCG-M5-2207-01 hCG-M5-2210-02
8 Am I Pregnant Pregnancy Midstream Test None** hCG-MHM-2205-01 hCG-MHM-2207-01 hCG-MHM-2207-02 hCG-MHM-2207-03 hCG-MHM-2207-04 hCG-MHM-2208-01 hCG-MHM- 209-01 hCG-MHM-2209-02 hCG-MHM-2209-03 HCG-MHM-2210-01 HCG-MHM-2210-02
9 hCG Pregnancy Strips None** hCG-S-2210-03
10 PrestiBio™ Breastmilk Alcohol Test Strip None**
11 PrestiBio™ Ovulation Strips*** None** Any Lot Number
12 PrestiBio™ Ovulation and Pregnancy Strips None** Any Lot Number
13 PrestiBio™ Pregnancy Strips**** None** Any Lot Number
14 PrestiBio™ Rapid Detection Pregnancy Test Midstream None** Any Lot Number
15 PrestiBio™ Ketone Test Strips None** Any Lot Number
16 PrestiBio™ Urinalysis Test Strip None** Any Lot Number
17 DiagnosUS® One Step LH Ovulation Test (Strip) None** LH-S-2204-01-S LH-S-2111-01-S
18 DiagnosUS® SARS-CoV-2 Antibody (IgG/IgM) Test None** COV-UL-2208-01
19 DiagnosUS® One Step FSH Menopausal Test (Strip None** FSH-S-2106-01 FSH-S-2108-01 FSH -S-2111-01-S
20 Lem Fertility hCG Pregnancy Urine Test None** hCG -S-2112-02
21 Lem Fertility LH Ovulation Test (Strip) None** LH-S-2112-01
22 DiagnosUS® hCG Pregnancy Urine Test Strip Format None** hCG-S-2101-01 hCG-S-2111-01-S hCG-S-2112-01
23 DiagnosUS® hCG Pregnancy Urine Test Cassette Format None** hCG-M5-2103-01 hCG-M5-2106-02 hCG- M5-2109-01 hCG- M5-2203-01
24 DiagnosUS® hCG Pregnancy Serum/Urine Test Cassette Format None** hCG-M5-2106-03
25 DiagnosUS® Pregnancy Test Midstream 710928980000 hCG-M11-2103-01 hCG-M11-2105-01
26 DiagnosUS® Ovulation Predictor Midstream 697691538914 LH-M11-2101-01 LH-M11-2105-01 LH-M11-2106-01 LH-M11-2107-01

Consumers who still have unused tests manufactured by Universal Meditech Inc. should stop using the device immediately and discard any remaining stock in the trash, or ship back to Universal Meditech at our expense.



Company name: Universal Meditech Inc.
Brand name: Healthy Wiser and more
Product recalled: Test kits
Reason of the recall: Product Safety/Defect
FDA Recall date: September 22, 2023

Source: www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/universal-meditech-inc-expands-nationwide-recall-all-products-manufactured-between-march-2021-and

#scam #ketogummiesscam #medicaldevices #unitedstates

Relatórios recentes perto de mim