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209 Fairfield Road, Fairfield, New Jersey, United States

Updated:

A
1. Employees are suffering from musculoskeletal disorders due to loading and unloading blood collection equipment from the trucks and also with assisting patients on and off the tables. 2. Employees have not received adequate ergonomic training. 3. Employees utilized chemical to clean equipment and patient collection tables … See More
have not received adequate training. 4. Employees have received needle sticks from equipment used in blood draws. 5. Employer has not performed a hazard assessment for employee exposed to patient to determine COVID exposure. 6. Employer has not provided proper PPE and training to employee for COVID exposure. 7. Employer is not properly recording COVID illness in the OSHA 300 logs. 8. Employee is not following CDC guidelines related to COVID precautions such as not being able to socially distance and are working in unventilated indoor spaces. 9. Employees are not being notified when they are exposed to donors/coworkers under investigation for COVID. 10. Employer is not ensuring that contracted cleaning services are properly disinfecting the worksites per the CDC guidelines.


Source: Osha.gov | Receipt Date: 2021-02-05
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#coronaviruscovid19 #osha #blood #209fairfieldroad #fairfield #newjersey #us

Recent Interesting Reports

C
I received a package containing SUBGENIX BIORIBOSE. MY OLD CARD WAS BILLED FOR THIS I didn't order it. Subsequently my card was cancelled. I'm waiting for my new one. I'm 20lbs under weight, the last thing I need is a weight loss supplement.

#unorderedpackage #delivery #virginiabeach #virginia #us

Aruba Aloe Balm N.V. is voluntarily recalling 40 lots of Aruba Aloe Hand Sanitizer Gel Alcohol 80% and Aruba Aloe Alcoholada Gel to the consumer level. The products have been found to contain alcohol denatured with methanol. Products were distributed between 5/1/2021 and 10/27/2023 and sold in … See More
the US online only via the Aruba Aloe Balm N.V. website. To date, Aruba Aloe Balm N.V. has not received any reports of adverse events related to these products.

Aruba Aloe Hand Sanitizer Gel is used as a sanitizer to help reduce bacteria that potentially can cause disease and is packaged in 12 fl oz (355 mL) dark green plastic bottles with white label reading in part “ARUBA ALOE Hand Sanitizer GEL 80% Alcohol Made in Aruba World’s Finest Aloe”, with barcode 0 82252 03300 5.

Aruba Aloe Alcoholada Gel is used for temporary relief of pain and itching associated with minor burns, sunburn, insect bites, or minor skin irritations and is packaged in two sizes: 2.2 fl oz (65 mL) plastic bottles with barcode 0 82252 34030 1 and 8.5 fl oz (251 mL) plastic bottles with barcode 0 82252 03120 9. The plastic bottles are transparent with a label reading in part “Alcoholada Gel Pain Relieving Gel 0.5% Lidocaine Hydrochloride”.

The affected Aruba Aloe Hand Sanitizer GEL product lots (filled in 12, 2.2, and 8.5 fl. oz bottles bottles) can be viewed in the link below.

Aruba Aloe Balm N.V. has notified all customers that bought these products by email and has offered a discount coupon for a next purchase. Consumers that have products which are being recalled should stop using and discard the product.

Risk Statement: Substantial methanol exposure can result in nausea, vomiting, headache blurred vision, coma, seizures, permanent blindness, permanent damage to the central nervous system, or death. Although all persons using these products on their hands are at risk, young children who accidently ingest these products and adolescents and adults who drink these products as an alcohol (ethanol) substitute are most at risk for methanol poisoning.

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: Aruba Aloe Balm N.V.
Brand name: Aruba Aloe
Product recalled: Hand Sanitizer Gel and Alcoholada Gel
Reason of the recall: Product contains methanol
FDA Recall date: April 05, 2024

Source: www.fda.gov
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#recall #us

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