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Covid-19 OSHA Complaint, Hospital General Menonita de Aibonito, Calle José C Vazquez, Aibonito, 00705, Puerto Rico

2 years ago

Covid-19 OSHA Complaint, Hospital General Menonita de Aibonito, Calle José C Vazquez, Aibonito, 00705, Puerto Rico

100 Calle José C Vazquez, Aibonito, 00705 Aibonito, Puerto Rico

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 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

#coronaviruscovid19 #osha #100callejosecvazquez #aibonito #aibonito #puertorico #soy

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Chloride Irrigation USP and Sterile Water for Irrigation USP. The Nurse Assist recall was issued due to the potential for a lack of sterility, which could result in non-sterile products. Medline Industries, LP has received one adverse event associated with product manufactured by Nurse Assist.

Water-based medical products that are non-sterile and potentially contaminated could cause serious or life-threatening infections, including bloodstream, urinary tract, open wound/soft tissue, and respiratory infections. Patients who are elderly, critically ill, have weak immune systems (including newborn infants, pregnant women, and cancer patients), or have chronic diseases are particularly at risk of infection. However, other patients could also develop infections after exposure to contaminated water-based medical products.

The recall affects Medline and Centurion convenience kits that may be used at home by patients, caregivers, and home health providers, as well as convenience kits that may be used in medical settings for surgery or other medical procedures. Recalled kits include, but are not limited to, wound care kits, tracheostomy kits and catheter kits. A detailed list of recalled Medline and Centurion convenience kits, as well as an example of product labeling, can be found in the link below.

Consumers who have recalled product should stop using the product and contact Medline immediately.

Medline Industries, LP notified its direct distributors and consumers of the Nurse Assist recall by First Class Mail and email on 11/16/23, upon receipt of initial recall notification from Nurse Assist. Customers who received the recalled product were given instructions to quarantine all affected products immediately and provide Medline with a response regarding the affected quantity on hand. Upon confirmation of the affected quantity, Medline provided customers with over-labels to place on the affected inventory, with instructions for staff to remove the affected component before using the kit. The recall notification also instructed distributors and those who resold or transferred affected product to another company or individuals to notify their customers of this recall notification.

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