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Target - Aurora West, Arapahoe County, CO

Latest report: March 9, 2022 12:00 PM
MN

2 individuals tested positive for Covid-19

2 years ago

2 individuals at Target - Aurora West in Arapahoe county tested positive for Covid-19. The outbreak began on 05/01/2022

Source: colorado.gov See Less
626


JF

7 individuals tested positive for Covid-19

2 years ago

7 individuals at Target - Aurora West in Arapahoe county tested positive for Covid-19. The outbreak began on 05-01-2022

Source: colorado.gov See Less
626


DV

11 individuals tested positive for Covid-19

2 years ago

11 individuals at Target - Aurora West in Arapahoe county tested positive for Covid-19. The outbreak began on 05-01-2022

Source: colorado.gov See Less
626


Related Reports

Nestlé USA has announced a recall of 440,500 Starbucks-branded ceramic mugs due to safety concerns. The mugs, which have a metallic coating, pose a burn and laceration hazard if microwaved or filled with extremely hot liquid. The company has reported 12 incidents of the mugs overheating or... See More breaking, resulting in 10 injuries. Nestlé USA is currently working closely with the U.S. Consumer Product Safety Commission on this recall.

The recalled mugs were sold in two sizes, 11 oz. and 16 oz., as part of four different gift sets during the 2023 holiday season. They were distributed at Target, Walmart, and Nexcom (military retail outlets) across the U.S. from November 2023 to January 2024. The recall does not affect any other Nestlé USA or Starbucks-branded products.

- Starbucks Holiday Gift Set with 2 Mugs (11 oz.). Retailer: Target.
- Starbucks Classic Hot Cocoa and Ceramic Mug (16 oz.). Retailers: Walmart, Nexcom.
- Starbucks Peppermint and Classic Hot Cocoa Ceramic Mug (16 oz.). Retailer: Target.
- Starbucks Holiday Blend Coffee and Mug (16 oz.). Retailers: Walmart, Nexcom.

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.

Source: nestleusa.com
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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: fda.gov
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Papa johns is not protecting their employees from COVID. I just got COVID and strep tested and it came back positive for both. They immediately told me to come back to work. This is completely unsanitary and unsafe for employees and customers. They are not following protocols... See More due COVID -19 and are disregarding everything just to have the correct amount of staffing. See Less
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A power outage was reported in Aurora, affecting rail service for three RTD rail lines. The E Line that runs from Union Station to RidgeGate Parkway Station in Lone Tree, the H Line that runs from the 18th and California Station to Florida Station in Aurora, and... See More the R Line from Lincoln Station in Lone Tree to Peoria Station in Aurora. According to Xcel Energy's outage map, power has been restored to the area.

Outage link: outagemap-xcelenergy.com
Source: denverpost.com
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I received an small package envelope from KERRY NOON, 8204 ROOSEVELT AVE, FLUSHING, NY 11377 to which I didn't place an order for this item. It's a knee pad, colored black with green design and green trimming

The package was shipped on 20 AUG 2013. The USPS... See More tracking number is 9200 1901 7554 7730 0448 046****

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Pkg came by USPS  did not order. Has Hazmat service transportation surface only.  Return to Jerry (001) Yasfbara 9208 Charles Smith Ave,Rancho Cucamonga ca91730.
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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: fda.gov
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Same story, but I don’t think I ordered anything like the jeans talked about here. I have no idea where it came from 😡 See Less
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Like many other people… 2 containers of product arrived each in its own bubble envelope… return address fulfillment house P.O. Box 5708 Tampa Fl…. Mailed to me 3-7-24 … phone number on container 800-609-4174…. Called it and no one speaks English

Myrtle Beach, SC See Less
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