Covid-19 OSHA Complaint, CVS Pharmacy #8794, 1600 North Buffalo Drive, LAS VEGAS, NV, 89128, USA

2 years ago

Covid-19 OSHA Complaint, CVS Pharmacy #8794, 1600 North Buffalo Drive, LAS VEGAS, NV, 89128, USA

1600 North Buffalo Drive, Las Vegas, 89128 Nevada, United States

1. A manager does not wear their face covering properly over their mouth and nose, potentially exposing employees to COVID-19. 2. A manager has continued to require employees that test positive for COVID-19 to come into work. Additionally, the manager required a symptomatic employee that had recently been exposed to COVID-19 to come into work and discouraged the employee from testing for COVID-19, potentially exposing other employees to COVID-19. Hazard Location: Throughout 1/10/2022 bm


Source: Osha.gov | Receipt Date: 2021-12-31

#coronaviruscovid19 #osha #cvspharmacy #1600northbuffalodrive #lasvegas #nevada #us

Related Reports

Brassica Pharma Pvt. Ltd. is voluntarily recalling the Eye Ointment products listed below with expiration dates ranging from February 2024 to September 2025. The products are being recalled due to a lack of sterility assurance. These products were distributed nationwide to wholesalers, retailers, and via the product … See More
distributors, Walmart, CVS, and AACE Pharmaceuticals Inc. To date, Brassica Pharma Pvt. Ltd. has not received any reports of adverse events up to 16th February 2024 related to this recall.

For those patients who use these products, there is a potential risk of eye infections or related harm. These products are intended to be sterile. Ophthalmic drug products pose a potentially heightened risk of harm to users because drugs applied to the eyes bypass some of the body’s natural defenses.

The affected products are:
- Product Name: Equate Lubricant Eye Ointment (Mineral Oil 42.5%, White Petrolatum 57.3%, Lanolin Alcohols), Package Description: 3.5-gram tube, packaged in a cardboard box, Brand Name: Equate, NDC: 79903-026-35, UPC Code: 681131395298.
- Product Name: Equate Stye Lubricant Eye Ointment (Mineral Oil 31.9%, White Petrolatum 57.7%, Microcrystalline Wax, Stearic Acid, Wheat Germ Oil), Package Description: 3.5-gram tube, packaged in a cardboard box, Brand Name: Equate, NDC: 79903-028-35, UPC Code: 681131395304.
- Product Name: CVS Health Lubricant Eye Ointment (Mineral Oil 31.9%, White Petrolatum 57.7%, Microcrystalline Wax, Stearic Acid Wheat Germ Oil, Package Description: 3.5-gram tube, packaged in a cardboard box, Brand Name: CVS Health, NDC: 76168-707-35, UPC Code: 050428634141.
- Product Name: Lubricant PM Ointment, Package Description: 3.5-gram tube, packaged in a cardboard box, Brand Name: AACE Pharmaceuticals, NDC: 71406-124-35, UPC Code: 371406124356.
For Lot number and expiry dates, you can visit the link below.

Brassica Pharma Pvt. Ltd. Is notifying its distributors AACE Pharmaceuticals Inc and its retailers Walmart and CVS. These distributors shall be further notifying the wholesalers and retailers via mail of this recall and arranging for return of all impacted products listed above. Consumers, distributors and retailers that have any product which is being recalled should cease distribution of the product. Consumers should stop using the recalled Eye Ointment and may return any of the above listed products to the place of purchase.

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: Brassica Pharma Pvt. Ltd.
Brand name: Multiple brands
Product recalled: Eye ointment products
Reason of the recall: Due to Potential Lack of Sterility Assurance.
FDA Recall date: February 26, 2024

Source: www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/brassica-pharma-pvt-ltd-issues-voluntary-nationwide-recall-equate-lubricant-eye-ointment-equate-stye
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Kilitch Healthcare India Limited is voluntarily recalling the eye drops products to the consumer level with all lots within expiry with expiration dates ranging from November, 2023 to September, 2025 for all the below mentioned products. These products are being recalled due to potential safety concerns after … See More
FDA investigators found insanitary conditions. These products were distributed nationwide to wholesalers, retailers, and via the product distributor, Velocity Pharma LLC. To date, Kilitch Healthcare India Limited has not received any reports of adverse events related to this recall.

Risk Statement: For those patients who use these products, there is a potential risk of eye infections or related harm. These products are intended to be sterile. Ophthalmic drug products pose a potentially heightened risk of harm to users because drugs applied to the eyes bypass some of the body’s natural defenses.

Affected products:

- Product: LUBRICATING TEARS EYE DROPS 15 ML. Product Information: Dextran 70- 0.1% w/v, Glycerin 0.2% w/v, Hypromellose 0.3% w/v. NDC NO: 0536-1282-94. Retailer / Label: Rugby.
- Product: Polyvinyl Alcohol 1.4% Lubricating Eye Drops 15 ml. Product Information: Polyvinyl alcohol Eye Drops 1.4% w/v. NDC NO: 0536-1325-94. Retailer / Label: Rugby.
- Product: High Performance Lubricant Eye Drops 15 ml (Single Pack). Product Information: Polyethylene glycol 400 0.4%, Propylene glycol 0.3% Eye Drops. NDC NO: 11673-522-15. Retailer / Label: Target.
- Product: High Performance Lubricant Eye Drops 15 ml (Twin Pack). Product Information: Polyethylene glycol 400 0.4%, Propylene glycol 0.3% Eye Drops. NDC NO: 11673-522-30. Retailer / Label: Target.
- Product: MULTI-ACTION RELIEF DROPS 15ML. Product Information: Polyvinyl alcohol 0.5% w/v, Povidone 0.6%w/v, Tetrahydrozoline 0.05% Eye Drops. NDC NO: 11822-2254-3. Retailer / Label: Rite Aid.
- Product: LUBRICATING GEL DROPS 10ML. Product Information: Polyethylene glycol 400 0.4%, Propylene glycol 0.3% Eye Drops. NDC NO: 11822-4540-3. Retailer / Label: Rite Aid.
- Product: LUBRICANT EYE DROPS 10ML (TWIN PACK). Product Information: Propylene glycol Eye Drops 0.6% w/v. NDC NO: 11822-4811-3. Retailer / Label: Rite Aid.
- Product: LUBRICANT GEL DROPS 15 ML. Product Information: Carboxymethylcellulose Sodium Eye Drops 1.0% W/V. NDC NO: 11822-9706-5. Retailer / Label: Rite Aid.
- Product: LUBRICANT EYE DROPS 15ML (TWIN PACK). Product Information: Carboxymethylcellulose Sodium Eye Drops 0.5% W/V. NDC NO: 11822-9707-5. Retailer / Label: Rite Aid.
- Product: Eye Irritation Relief 15 ml. Product Information: Polyvinyl alcohol 0.5% w/v, Povidone 0.6%w/v, Tetrahydrozoline 0.05% Eye Drops. NDC NO: 70000-0087-1. Retailer / Label: Leader.
- Product: Dry Eye Relief 10 ml. Product Information: Polyethylene glycol 400 0.4%, Propylene glycol 0.3% Eye Drops. NDC NO: 70000-0088-1. Retailer / Label: Leader.
- Product: Dry Eye Relief 15 ml. Product Information: Carboxymethylcellulose Sodium Eye Drops 1.0% W/V. NDC NO: 70000-0089-1. Retailer / Label: Leader.
- Product: Lubricant Eye Drops 15 ML (Single Pack). Product Information: Carboxymethylcellulose Sodium Eye Drops 0.5% W/V. NDC NO: 70000-0090-1. Retailer / Label: Leader.
- Product: Lubricant Eye Drops 15 ML (Twin Pack). Product Information: Carboxymethylcellulose Sodium Eye Drops 0.5% W/V. NDC NO: 70000-0090-2. Retailer / Label: Leader.
- Product: Lubricant Eye Drops 10 ml. Product Information: Propylene glycol Eye Drops 0.6% w/v. NDC NO: 70000-0587-1. Retailer / Label: Leader.
- Product: LUBRICANT EYE DROP 10ML (TRIPLE PACK). Product Information: Propylene glycol Eye Drops 0.6% w/v. NDC NO: 76168-502-30. Retailer / Label: Velocity.
- Product: Lubricant Eye Drops 15 ML (Single Pack). Product Information: Carboxymethylcellulose Sodium Eye Drops 0.5% W/V. NDC NO: 76168-702-15. Retailer / Label: CVS.
- Product: Lubricant Eye Drops 15 ML (Twin Pack). Product Information: Carboxymethylcellulose Sodium Eye Drops 0.5% W/V. NDC NO: 76168-702-30. Retailer / Label: CVS.
- Product: Lubricant Gel Drops 15 ml (Single Pack). Product Information: Carboxymethylcellulose Sodium Eye Drops 1.0% W/V. NDC NO: 76168-704-15. Retailer / Label: CVS.
- Product: Lubricant Gel Drops 15 ml (Twin Pack). Product Information: Carboxymethylcellulose Sodium Eye Drops 1.0% W/V. NDC NO: 76168-704-30. Retailer / Label: CVS.
- Product: Multi Action Relief Drops 15 ml. Product Information: Polyvinyl alcohol 0.5% w/v, Povidone 0.6%w/v, Tetrahydrozoline 0.05% Eye Drops. NDC NO: 76168-706-15. Retailer / Label: CVS.
- Product: MILD MODERATE LUBRICATING EYE DROPS 15ML. Product Information: Polyethylene glycol 400 0.4% w/v. NDC NO: 76168-711-15. Retailer / Label: CVS.
- Product: Lubricant Gel Drops 10 ml. Product Information: Polyethylene glycol 400 0.4%, Propylene glycol 0.3% Eye Drops. NDC NO: 76168-712-10. Retailer / Label: CVS.
- Product: Lubricant Eye Drops 10 ml (Single Pack). Product Information: Propylene glycol Eye Drops 0.6% w/v. NDC NO: 76168-714-10. Retailer / Label: CVS.
- Product: Lubricant Eye Drops 10 ml (Twin Pack). Product Information: Propylene glycol Eye Drops 0.6% w/v. NDC NO: 76168-714-20. Retailer / Label: CVS.
- Product: DRY EYE RELIEF 15 ML (TWIN PACK). Product Information: Carboxymethylcellulose Sodium Eye Drops 0.5% W/V. NDC NO: 76168-800-30. Retailer / Label: Target.
- Product: EQUATE HYDRATION PF LUBRICANT EYE DROPS 10ML. Product Information: Polyethylene glycol 400 0.4%, Propylene glycol 0.3% Eye Drops. NDC NO: 79903-168-01. Retailer / Label: Walmart.

Consumers, distributors, and retailers that have any product that is being recalled should cease distribution of the product. Consumers should stop using the recalled eye drops and may return any of the products to the place of purchase.

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: Kilitch Healthcare India Limited
Brand name: Multiple brands
Product recalled: Lubricant Eye Drops & Multi-Symptom Eye Drops
Reason of the recall: Device & Drug Safety Potential Safety Concerns
FDA Recall date: November 15, 2023

Source: www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/kilitch-healthcare-india-limited-issues-voluntary-nationwide-recall-various-eye-drops-potential
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Fedex is the same way. Woman I worked with was threatened by management that if she didn't report to work even though being positive and symptomatic, she would be fired!

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You are a f**king moron.

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Floor cracks are getting wider and destroying our PIT equipment, walls are uneven and mold is at an all time high as employees struggle to breathe comfortably in the warehouse. Mold in floor cracks and between walls and boxes. Low quality concrete floor unsafe to support 6 ton PIT.

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Keto Genesis, Las Vegas, NV, USA

1 day ago •reported by user-fvzy2297

Ordered 3 bottles of Keto Genesis gummies and got 2 free. With the order I also received 2 bottles of detox that I did not order. I was charged $59 for the detox and $199 for the gummies. I called the company got an RMA returned the … See More
detox, cost me $7.50 shipping. Was told I would get a credit in 5 - 7 business days after they received it back. This package was received on 3/16/24. After speaking with my doctor I was told not to take the gummies because of all the other meds I take. I called, same RMA number returned the 5 bottles at a shipping cost of $32, they received that on April 1st. Still haven't seen a credit. I called them today and guess what, they JUST TODAY got authorization to refund my credit card... BUT they are charging me restocking fees that no one ever mentioned before. This whole debacle is costing me $114.54 and I'm getting nothing for it. I want them reported for the scammers that they are, I want all my money back I don't want to pay for this. This is definitely a scam I am so pissed off
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I want to send the unordered gummies back !, Las Vegas, NV, USA

3 days ago •reported by user-mygy3628

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stop any future orders??
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Ketogenesis scam, Las Vegas, Nevada, USA

3 days ago •reported by user-ffhdg745

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Recent Interesting Reports

Amneal Pharmaceuticals, LLC. Bridgewater, New Jersey (Amneal), is voluntarily recalling 4 lots (see table below) of Vancomycin Hydrochloride for Oral Solution, USP, 250 mg/5mL packaged in 80 mL, 150 mL, or 300 mL pack sizes, to the Consumer Level. Some bottles may have been overfilled which can … See More
result in an over-potent dosing regimen. The affected Vancomycin Hydrochloride for Oral Solution, USP, 250 mg/5mL lots were distributed Nationwide in the USA directly to Wholesalers and Distributors. The Lots were distributed between 11/09/2023 and 2/20/2024. To date, Amneal has not received any reports of adverse events that have been confirmed to be directly related to this recall.

Risk Statement: Adult patients who are prescribed the maximum daily dose of up to 2 grams per day of Vancomycin Hydrochloride for oral solution, USP 250 mg/5mL, may receive up to 4 grams of oral vancomycin per day because of the overfilled bottle. Some patients with inflammatory disorders of the intestinal mucosa also may have significant systemic absorption of vancomycin. These patients may be at risk for the development of adverse reactions associated with higher doses of vancomycin oral solution. Worsening renal function could be associated with electrolyte abnormalities such as high potassium leading to cardiac arrest.

The recommended maximum daily dose allowance for this product is up to 2gm/day and patients prescribed a dosing regimen of 500 mg/10mL would exceed this daily allowance, which may be harmful to patients with renal insufficiency. The error occurred during the manual bottle filling stage of manufacturing.

Vancomycin Hydrochloride for Oral Solution, USP, 250mg/5mL, is administered orally for treatment of enterocolitis caused by Staphylococcus aureus (including methicillin-resistant strains) and antibiotic- associated pseudomembranous colitis caused by C. difficile.

The Vancomycin HCl for Oral Solution, USP, 250 mg/5mL subject to the recall, are identified by the NDC numbers stated on the product label. The following lot numbers of Vancomycin Hydrochloride for Oral Solution, USP, 250 mg/5mL are included in this recall.

Vancomycin Hydrochloride for Oral Solution, USP, 250mg/5mL.
- Pack Size: 80 mL, Expiration Date: 09/2025, Lot: 22613003A, NDC No.: 69238-2261-3.
- Pack Size: 150 mL, Expiration Date: 09/2025, Lot: 22613004A, NDC No.: 69238-2261-7.
- Pack Size: 150 mL, Expiration Date: 09/2025, Lot: 22613005A, NDC No.: 69238-2261-7.
- Pack Size: 300 mL, Expiration Date: 09/2025, Lot: 22613005B, NDC No.: 69238-2261-5.

Anyone with an existing inventory of the product being recalled should examine the product and quarantine any of the recalled lots immediately. Retailers who have Vancomycin Hydrochloride for Oral Solution, USP, 250 mg/5mL, which are being recalled, should examine their inventory and cease dispensing any of the impacted lots.

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: Amneal Pharmaceuticals, LLC.
Brand name: Amneal
Product recalled: Vancomycin Hydrochloride for Oral Solution, USP, 250 mg/5mL
Reason of the recall: Super potent due to bottles being overfilled
FDA Recall date: March 27, 2024

Source: www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/amneal-pharmaceuticals-llc-issues-nationwide-voluntary-recall-vancomycin-hydrochloride-oral-solution
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