Hospital General Menonita de Aibonito, Calle José C Vazquez, Aibonito, 00705, Puerto Rico
Latest report:
Covid-19 OSHA Complaint
2 years ago
I am a hospital employee and we have currently received both suspicious and covib positive patients and employees. Because of this we are afraid as the institution provides us with 2 surgical masks for the shift which are not 100% effective in hospitals, some employees pay kn95
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and n95 masks but Mrs [PII] of internal infection control does not allow us to use them since there is an internal guideline to use only those provided by the hospital. If we are provided with face shield and we are allowed to wear safety glasses, but in a unit where it is full there are 24 patients with the rooms closed by institutional regulations. These patients locked up in a TV room, who are mentally ill and most of the time do not wear masks well and the hospital provides only 1 per day and if it is ugly it changes sometimes, to top it off in that little room is that they take therapy without any social distancing, It is totally unacceptable and risky both for patients and family members as for all staff. In addition to this, the hospital is currently remodeling the area of the employee's toilets and we only have one employee who is next to the one under construction and the dust and noise is immense as well as if the higen of everyone using that bathroom is terror. We can use the ones in front but these are used by patients and the administration area is closed for use by patients. In many cases and seen the employees of this remodeling without a helmet or safety goggles and misplaced masks are several risks of exposure I ask to investigate as soon as possible.
Alleged Hazards: 1, Employees Exposed: 20
Source: Osha.gov | Receipt Date: 2020-08-04
Alleged Hazards: 1, Employees Exposed: 20
Source: Osha.gov | Receipt Date: 2020-08-04
8
Covid-19 OSHA Complaint
3 years ago
With the COVID19 situation we have limited materials exposing us to situations of risk due to lack of equipment. We have a lack of protocols and staff guidance. Medical faculty and administration do not agree on how to handle the situation by exposing us. Hazard Location: Specifically
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in the area of hospitalization floors that are 4. Also in the emergency room and the hospital in general (respiratory therapy, floor secretaries, etc.) is putting employees at risk of contagion
Alleged Hazards: 1, Employees Exposed: 20
Source: Osha.gov | Receip Date: 2020-03-18
Alleged Hazards: 1, Employees Exposed: 20
Source: Osha.gov | Receip Date: 2020-03-18
9
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3 weeks ago •source www.fda.gov
Recall notice
FAonline INC, is voluntarily recalling all lots within expiry of the ForeverMen capsules to the consumer level. FDA analysis founds these products to be tainted with sildenafil and Tadalafil. Sildenafil/Tadalafil is an FDA approved drug for the treatment of erectile dysfunction, the presence of sildenafil in the
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Risk Statements: Men with diabetes, high blood pressure, high cholesterol, or heart disease, may be on medications that if taken with these products could lower blood pressure to dangerous levels that could be life threatening. The products affected are men with diabetes, high blood pressure, high cholesterol, or heart disease.
The product is marketed as dietary supplements for male sexual enhancement and is packaged in a blister card. 10 count box. We are notifying the public through this public announcement due to lack of ability to identify customers who may have received the product. FAonline INC. is notifying its customers that have the ForeverMen products to stop use and properly discard the product.
Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to taking or using this drug product.
In case you experienced harm from allergens or undeclared ingredients, it is important to report it. It can help to detect & resolve issues and prevent others from being harmed, and it enables better surveillance. If symptoms persist, seek medical care.
Company name: FAonline Inc
Brand name: ForeverMen
Product recalled: Natural Energy Boost
Reason of the recall: Product is tainted with sildenafil and tadalafil
FDA Recall date: April 02, 2024
Source: www.fda.gov
Risk Statements: Men with diabetes, high blood pressure, high cholesterol, or heart disease, may be on medications that if taken with these products could lower blood pressure to dangerous levels that could be life threatening. The products affected are men with diabetes, high blood pressure, high cholesterol, or heart disease.
The product is marketed as dietary supplements for male sexual enhancement and is packaged in a blister card. 10 count box. We are notifying the public through this public announcement due to lack of ability to identify customers who may have received the product. FAonline INC. is notifying its customers that have the ForeverMen products to stop use and properly discard the product.
Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to taking or using this drug product.
In case you experienced harm from allergens or undeclared ingredients, it is important to report it. It can help to detect & resolve issues and prevent others from being harmed, and it enables better surveillance. If symptoms persist, seek medical care.
Company name: FAonline Inc
Brand name: ForeverMen
Product recalled: Natural Energy Boost
Reason of the recall: Product is tainted with sildenafil and tadalafil
FDA Recall date: April 02, 2024
Source: www.fda.gov
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