Covid-19 OSHA Complaint, Pulse Medical Transporation, 264 Lakawanna Ave., WOODLAND PARK, NJ, 07424, USA

2 years ago

Covid-19 OSHA Complaint, Pulse Medical Transporation, 264 Lakawanna Ave., WOODLAND PARK, NJ, 07424, USA

24 Andrews Drive, Woodland Park, 07424 New Jersey, United States

Allegation 1) Employees who provide ambulatory care to confirmed and suspected COVID-19 patients are required to wear N95 respirators and have not completed an initial fit test. Allegation 2) Employees are provided with disposable mesh gowns that are inadequate. The gowns become saturated, allowing infectious material to permeate through the material. Allegation 3) The employer, after learning that an employee was confirmed positive for COVID-19, did not inform affected employees, of their potential exposure to COVID-19. The affected employees worked alongside an employee who tested positive for COVID-19.

Alleged Hazards: 3, Employees Exposed: 50
Source: Osha.gov | Receipt Date: 2020-11-17

#coronaviruscovid19 #osha #24andrewsdrive #woodlandpark #newjersey #us

747

Recent Interesting Reports

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Scam alert, 192-01 Northern Blvd, Flushing, NY, USA

5 days ago •reported by user-fmgdv214

I received a Daily Detox from SlimFit Fusion in Flusing NY that I did not order

I received to packages, the last one fro DP 192-01 Northern Blvd. Flusing NY. It was for Daily Detox by Slim Fit Fusion. I also received another package Keto+ACV. Neither were ordered

#ketogummiesscam #unorderedpackage #delivery #newyork #us

Scam alert photo #1
1.4K

Honeywell Non-Sterile Eyewash Cartridge - recalled due to Non-compliance, USA

1 week ago •source www.fda.gov

Recall notice

Honeywell Safety Products USA, Inc. is voluntarily recalling Fendall 2000 Non-Sterile Eyewash Cartridge for the Fendall 2000 Eyewash Station. This recall is being conducted at the industrial consumer level. Honeywell’s supplier of the Fendall 2000 Non-Sterile Eyewash Cartridge has been found to be non-compliant with current good … See More
manufacturing practice (cGMP) requirements. To date, Honeywell Safety Products USA, Inc. has not received any reports of adverse events related to this recall.

The Fendall 2000 Non-Sterile Eyewash Cartridge is used for flushing or irrigating the eye to reduce chances of severe injury caused by acid, alkali, or particulate contamination. Product is contained in a 25-liter Ethylene-vinyl acetate (EVA) bag that is designed for use with the Fendall 2000 Eyewash Station. Only the Fendall 2000 refill cartridges are subject to this review, no other eyewash products. The saline eyewash solution contains purified water, benzalkonium chloride, edetate disodium, sodium chloride, sodium phosphate diabasic, and sodium phosphate monobasic. It is not marketed as sterile.

- Fendall 2000 Non-Sterile Eyewash Cartridge. Manufacturer’s Product Number/ Catalog Number: 32-002050-0000. Manufacturing Dates: 11-Oct- 2021 through 21-Jun-2023. Expiration Date: 11-Oct-2023 through 21-Jun-2025. Region: USA. Quantity: 6,954.

- Fendall 2000 Non-Sterile Eyewash Cartridge. Manufacturer’s Product Number/ Catalog Number: 32-002050-0000. Manufacturing Dates: 11-Oct- 2021 through 21-Jun-2023. Expiration Date: 11-Oct-2023 through 21-Jun-2025. Canada. Quantity: 3,651

Honeywell Safety Products USA, Inc. is notifying its distributors and customers by email, telephone or certified mail and is requesting anyone with product in its inventory to destroy or dispose of all units subject to the recall. Customers / distributors / retailers that have Fendall 2000 Non-Sterile Eyewash Cartridges should stop selling, shipping, and using the product immediately and destroy or dispose of it. Customers with questions regarding this recall can contact Honeywell Safety Products USA, Inc. by telephone.

Risk Statement: Use of or exposure to the eyewash without seeking medical attention afterwards could result in a range of ocular infections such bacterial keratitis or endophthalmitis. Immunocompromised individuals, those sustaining ocular injuries that damage the corneal epithelium, and those sustaining penetrating ocular injuries are at higher risk of potential infection.

Company name: Honeywell Safety Products USA
Brand name: Fendall 2000
Product recalled: Non-Sterile Eyewash Cartridge
Reason of the recall: Non-compliance with current good manufacturing practice (cGMP) requirements.
FDA Recall date: April 05, 2024

Source: www.fda.gov
See Less

#recall #drugs #us

Honeywell Non-Sterile Eyewash Cartridge - recalled due to Non-compliance photo #1
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D

I am reporting a scam, 746 South Glasgow Avenue, Inglewood, CA, USA

3 weeks ago •reported by user-dfrqy463

I ordered a package from Facebook advertisement that was supposed to be Amazon warehouse returns. I paid nearly $40 and today a package was received called MYSTERY BOX which contained a cheap smart watch! Total ripoff !!!

Im in Mount Vernon, IL, USA

#scam #facebookscam #delivery #746southglasgowavenue #inglewood #california #us

I am reporting a scam photo #1
2.8K

Alert of a cluster of Illnesses resembling Botulism from possibly Counterfeit Botox, LaSalle County, IL, USA

1 week ago •source dph.illinois.gov

Outbreak

The Illinois Department of Public Health (IDPH) has issued an alert regarding a potential botulism outbreak linked to possibly counterfeit Botox injections. The alert follows the hospitalization of two individuals in LaSalle County who exhibited symptoms similar to botulism after receiving the injections. The issue came to … See More
light after the patients presented with symptoms resembling botulism. The IDPH, in collaboration with the LaSalle County Health Department and the Illinois Department of Professional Regulation (IDFPR), is currently investigating the matter. A similar cluster of cases was also reported by the Tennessee Department of Health, prompting the IDPH to liaise with the CDC and FDA for further investigation.

The product in question is either Botox or a possibly counterfeit version of the product, and it was administered by a licensed nurse in LaSalle County who was performing work outside her authority. The two affected individuals reported symptoms such as blurred/double vision, droopy face, fatigue, shortness of breath, difficulty breathing, and hoarse voice following the injection. Both required hospitalization post-treatment.

People are advised not to use these botox injections. In Illinois, the injection of botulinum toxin, the key ingredient in Botox, is a practice of medicine that may only be performed by certain licensed professionals who are licensed and regulated by IDFPR. Cosmetologists and estheticians are prohibited from performing this practice under their licenses.

Botulism is a serious illness caused by a toxin produced by the Clostridium botulinum bacteria. This toxin is one of the most potent neurotoxins known and can cause muscle paralysis. The disease can manifest in three forms: foodborne botulism, wound botulism, and infant botulism. Foodborne botulism, which is the focus here, occurs when food contaminated with the bacteria is consumed. Symptoms can include difficulty swallowing or speaking, facial weakness, and paralysis. In severe cases, it can be fatal, particularly if it affects the respiratory muscles.

If you or a loved one are harmed or experiencing any symptoms, it is important to report it. Reporting can help to detect & resolve outbreaks early and prevent others from being harmed, and enables better surveillance. If symptoms persist, seek medical care.

Source: dph.illinois.gov
See Less

#illinois #us #botulism

Alert of a cluster of Illnesses resembling Botulism from possibly Counterfeit Botox photo #1
27

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