Halifax County - Department of Social Services, 4421 U.S. 301, HALIFAX, NC, 27839, USA
Latest report:
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Covid-19 OSHA Complaint
3 years ago
1. As of November 4, 2020, there have been (15) cases of COVID-19 in the facility, including one death and one employee being hospitalized. Employees are concerned about the cleaning that is being done and feel that a professional cleaning crew should come in to clean. Employees
are told that a maintenance crew is spraying something after they leave and employees are required to come into the building to work the next day. Employees feel that the building should be closed for period of time to allow for a thorough cleaning and for employees to work away from the building and not be exposed to the virus. 2. There has been a mold problem in the building. The air vents and ceiling are brown from water leaks. Employees with pre-existing conditions are working together in a small room that is closed with poor ventilation, in order to be away from areas that may have mold. 3. Yellow anti-slip strips on the concrete steps employees use to enter the buiding have come off and the concrete has crumbed. A cone has been placed on the steps and it and the crumbling concrete cause a trip/fall hazard.
Source: Osha.gov | Receipt Date: 2020-11-04
Source: Osha.gov | Receipt Date: 2020-11-04
217
Covid-19 OSHA Complaint
3 years ago
There has been an outbreak of COVID-19 at the facility and staff are told that they must continue to report to work. A number of people have been tested positive. A majority of staff from the adult/family and children medicaid unit are out to to either having
COVID-19 or having symptoms. There are concerns that proper precautions are not being taken. 1. Employees are concerned that adequate cleaning and sanitizing has not been conducted. There has been cleaning done twice, but staff members remained in the building each time while cleaning was done. Employees feel that there should be a deep cleaning done without employees present in the building. Employees are being told that they must clean their own work areas. 2. Staff members have been exposed to positive COVID-19 cases and have expressed an interest in getting tested. If they have no personal time available to use while getting tested, they will receive disiplinary action if out of work to be tested for COVID-19. This is causing employees to not be tested for the virus.
Source: Osha.gov | Receipt Date: 2020-11-03
Source: Osha.gov | Receipt Date: 2020-11-03
217
Covid-19 OSHA Complaint
3 years ago
There have been a lot of employees that have tested positive for COVID-19 and the facility has not been closed or sanitized. Employees are concerned due to having to continue to work in the building and that they have potentially been exposed to the virus due to
contact with others.
Source: Osha.gov | Receipt Date: 2020-11-05
Source: Osha.gov | Receipt Date: 2020-11-05
217
Covid-19 OSHA Complaint
3 years ago
Employees could be exposed to the COVID-19 virus in the workplace, due to: 1. There have been 8 confirmed cases in the last week, and it appears to be spreading in the building; 2. Only the immediate work area of affected employees has been sanitized: common, heavily
used areas are not receiving any special attention.
Source: Osha.gov | Receipt Date: 2020-10-26
Source: Osha.gov | Receipt Date: 2020-10-26
217
Recent Interesting Reports
Online Scam, 2800 North Franklin Road, Indianapolis, IN, USA
4 weeks ago •reported by user-jcbt2612
I received an item that was not an air bed mattress that I purchased and received a necklace instead and would like to report. Just like others, I saw when I googled this address because I did not recognize the item which was a black necklace type
that I would not order nor in place of an air bed mattress which I received an alert on my email that it was delivered. I have a picture, but I don’t see how I can send, or add an attachment
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3 weeks ago •reported by user-wjzp6244
I received this package in the mail and I never ordered anything, from this place called Fullfillment House PO Box 10205 Tampa FL 33679-0205, they have charged me 3 x on my credit card, first charges was on March 24 2024 one charge for $ 60.09, and
another charge for $99.00 on the same day, then again on April 4 2024 for 60.09.
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Received a keto pure bioribose that I did not order., Myrtle Point, Oregon, USA
5 days ago •reported by user-kczw1921
I received a small container (1 oz.) of Keto Pure Bioribose that I did not order. It was manufactured for: Keto Pure, Tampa, Florida 33626, 877-211-5175
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I received a package that I never ordered, Williamstown, Monroe, NJ, USA
3 weeks ago •reported by user-gtvfp911
I just received a package with a t-shirt in size small (I wear medium) that I did not order. I was not charged so I will donate to a local charity.
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Medline and Centurion Convenience kits - recalled due to lack of sterility, USA
3 weeks ago •source www.fda.gov
Recall notice
In direct response to the Nurse Assist, LLC voluntary product recall initiated on November 6, 2023, for saline and sterile water medical products, Medline Industries, LP initiated a nationwide recall on November 15, 2023, for its Medline and Centurion branded convenience kits containing Nurse Assist 0.9% Sodium
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.
In case you experience harm from this product, 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: Medline Industries, LP
Brand name: Medline and Centurion
Product recalled: Convenience kits
Reason of the recall: The potential for a lack of sterility
FDA Recall date: April 08, 2024
Source: www.fda.gov
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.
In case you experience harm from this product, 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: Medline Industries, LP
Brand name: Medline and Centurion
Product recalled: Convenience kits
Reason of the recall: The potential for a lack of sterility
FDA Recall date: April 08, 2024
Source: www.fda.gov
303
Scammed by Heather's Motty, 2207 Summit Avenue, Union City, NJ, USA
3 weeks ago •reported by user-jxhnt677
I ordered a starlink wi-fi. Received 2 gree dots.
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