Lowe's Home Improvement, 3400 North Texas Street, FAIRFIELD, CA, 94533, USA
Latest report:
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Covid-19 OSHA Complaint
2 years ago
1. The employer did not ensure to clean and disinfect areas, materials and equipment used indoors by a COVID-19 case if the area is to be used by another employee within 24 hours. T8 CCR 3205(c)(7)(B)(2). 2. The employer did not ensure to make COVID-19 testing available
to employees in the exposed workgroup immediately upon being covered by this section. T8 CCR 3205.1(c)(2)(A). 3. The employer did not ensure that employees in the exposed workgroup wear facial coverings when indoors, outdoors and when closer than 6 feet from other persons. T8 CCR 3205.1(d)(1). 4. The employer did not ensure to exclude unvaccinated employees who were exposed to a COVID-919 case from the workplace until the requirements of subsection (c)(10) are met. T8 CCR 3205(c)(9)(B). 5. The employer did not ensure that facial coverings were provided and worn by all unvaccinated employees at the Fairfield store location. T8 CCR 3205(c)(6)(A). 6. The employer did not ensure that employees who were exposed to a known COVID-19 case during the high-risk exposure period were given notification of the exposure within one business day. T8 CCR 3205(c)(3)(3).
Alleged Hazards: 6, Employees Exposed: 1
Source: Osha.gov | Receipt Date: 2021-07-29
Alleged Hazards: 6, Employees Exposed: 1
Source: Osha.gov | Receipt Date: 2021-07-29
120
Covid-19 OSHA Complaint
3 years ago
The employer did not maintain an effective injury and illness prevention program in that the employer did not ensure that COVID-19 precautions per the state executive and local public health department orders are being followed at the workplace in the following instances: 1. The employer did not
ensure to exclude COVID-19 cases from the work place until the return to work criteria in subsection (c)(11) had been met. Ref T8CCR 3205(c)(10)(A). 2. The employer did not give notice to employees on their exposure to a COVID-19 positive case in the workplace. Ref T8CCR 3205(c)(3)(B)(3). 3. The employer did not identify and disinfect areas, materials and equipment used by a COVID-19 case in the workplace. Ref T8CCR 3205(c)(8)(C)3.
Alleged Hazards: 3, Employees Exposed: 1
Source: Osha.gov | Receipt Date: 2020-12-28
Alleged Hazards: 3, Employees Exposed: 1
Source: Osha.gov | Receipt Date: 2020-12-28
120
Covid-19 OSHA Complaint
3 years ago
The employer did not maintain an effective injury and illness prevention program in that the employer did not ensure that COVID-19 precautions per the state executive and local public health department orders are being followed at the workplace in the following instances: 1. The employer did not
give notice to employees on their potential exposure to a COVID-19 Positive case, T8 CCR 3205(c)(3)(B)(3).
Alleged Hazards: 1, Employees Exposed: 1
Source: Osha.gov | Receipt Date: 2020-12-08
Alleged Hazards: 1, Employees Exposed: 1
Source: Osha.gov | Receipt Date: 2020-12-08
120
Recent Interesting Reports
Scam! Received a product that is totally different than advertised!, 192-01 Northern Boulevard, Flushing, NY, USA
2 days ago •reported by user-tvrc3773
The “air purifier” I purchased is definitely not what was advertised when I purchased the item! The price was 2-4 times more than advertised on other sites and it is no where close to being capable of doing what it claimed online.
1.4K
scam charge my deit for something I nevered ordered, San Antonio, TX, USA
2 weeks ago •reported by user-rcnxw335
I discovered today that my deit card was charded 109.79 for something I never ordered
710
I just received a bottle of Subgenix Bioribose that I didn’t order., Kings Mountain, NC, USA
3 weeks ago •reported by user-dvtj7516
I just received this package today and I am not sure what it is and why it was sent to me.
51
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
Unordered package, Indianapolis, IN, USA
2 weeks ago •reported by user-tryvb786
I received a package I didn’t order. SUBGENIX
BIORIBOSE
Ingrove Dveral Metabolism Through Actiation ofAMPK PSC-H'
Provides Non-Stimulant Energy Boost *
Benefits Occur With and Without Exercise*
DIETARY SUPPLEMENT D
BIORIBOSE
Ingrove Dveral Metabolism Through Actiation ofAMPK PSC-H'
Provides Non-Stimulant Energy Boost *
Benefits Occur With and Without Exercise*
DIETARY SUPPLEMENT D
449
Package I did not order, Cobblestone Lane, Beloit, WI 53511, USA
4 weeks ago •reported by user-fzjhk432
On April 1, 2024 I found a package that I did not order. The return address is Shipping Center, 609 Cattle Chute Ct, Celina TX 75009
52
I got a dress I don’t order, El Paso, TX, USA
2 weeks ago •reported by user-vhxdb428
I received a something the looked like a dress it is horrible, I don’t even like or how much you charge for it.
280
Unordered bottle of subgenix, Cincinnati, OH, USA
3 weeks ago •reported by user-dmyr4973
Received a random bottle of subgenix and had no idea what it was until I googled it. Not sure what to do with it or where it came from.
490
I did not order all this, Nebraska 2, Grand Island, NE, USA
2 weeks ago •reported by user-dpxw9319
I only ordered two I didn’t order five more and I’d like my money back for the ones that I did not order and I want you to cancel it altogether
29
Ring sent I did not order from California, From California im in tucson
2 weeks ago •reported by user-tkvjf322
Recieved a ring I did not order. From unknown seller out of California. Googled the address and says it's just a house not a business.
Last 30 days