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Target, 275 South River Road, SAINT GEORGE, UT, 84790, USA

Latest report: January 14, 2021 12:00 PM
TD

Covid-19 OSHA Complaint

3 years ago

1. Employees not wearing masks in the store. 2. No enforcement of mask mandate by management.


Source: Osha.gov | Receipt Date: 2020-12-03 See Less
43


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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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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
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FDA Recall date: March 27, 2024

Source: fda.gov
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Shipment number F4****** (293991981603500******* has been changed from status uncollected to status active, at 14-03-2024 10:50:25.
Client reference: BL31624031120******

Sender: HONGKONG LINGXIA TRADING LIMITED
Sender address: Vecsés, Bud Cargo City 325 bld. Ghibli Kft. 2220, Forwarder bldg W10 Budapest Budapest

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