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Covid-19 OSHA Complaint, Walmart fulfillment, 6750 Kimball Ave, Chino, California 91708, USA

3 years ago

6750 Kimball Avenue, Chino, 91708 California, United States

T8CCR 3203(a)(4) - There are three cases of positive COVID-19. The breakroom and work areas are not sanitized or clean.

Alleged Hazards: 1, Employees Exposed: 1
Source: Osha.gov | Receipt Date: 2020-07-10

702


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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: www.nestleusa.com/media/pressreleases/metallicmugrecall
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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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San Luis, AZ, G.A. Mart dba H&Natural, is voluntarily recalling 2 lots of H&NATURAL TejoRoot, 10g pills, and 2 lots of H&NATURAL Brazil Seed, .167g Seeds to the consumer level. The products have been found via random FDA testing to contain yellow oleander, a poisonous plant native... See More to Mexico and Central America. H&NATURAL TejoRoot and H&NATURAL Brazil Seed were distributed Nationwide to via internet on their site, Amazon.com, and Walmart.com. The company has received one report of gastrointestinal illness, including painful symptoms in conjunction with internal bleeding in connection with H&NATURAL TejoRoot, and has not received any reports of adverse events in connection with H&NATURAL Brazil Seed.

Risk Statement: Ingestion of yellow oleander can cause neurologic, gastrointestinal, and cardiovascular adverse health effects that may be severe, or even fatal. Symptoms may include nausea, vomiting, dizziness, diarrhea, abdominal pain, cardiac changes, dysrhythmia, and more.

The recalled dietary supplements can be identified by the H&NATURAL logo and the following descriptions:
- Tejo Root, Raiz de Tejocte, H&Natural, Healthy, and Natural, Dietary Supplement, 10g pills, is packaged in a box or bottle, with UPC (196852946921)
- Brazil Seed Pure Natural Semilla de Brasil, H& Natural, Healthy and Natural, 0.167g seeds, packaged in a box or bottle, with UPC (195893047529) (196852820641) (195893698721) (195893236893)(196852134618) (195893336975)

Recalled lots are labeled with the following expiration dates, 3/24 and 5/24.

Consumers that have the recalled H&NATURAL TejoRoot or H&NATURAL Brazil Seed lots should stop using the products. Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to taking or using this drug product.

In case you experience harm from extraneous materials, 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: G.A. Mart dba H&Natural
Brand name: H&Natural
Product recalled: Brazil Seed Pure Natural Semilla de Brasil & Tejo Root, Raiz de Tejocte
Reason of the recall: Product contains yellow oleander, a poisonous plant
FDA Recall date: February 23, 2024

Source: www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/ga-mart-issues-voluntary-nationwide-recall-hnatural-tejoroot-and-hnatural-brazil-seed-dietary
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T8CCR 3205- Currently work at the California Institution for Men in Personnel. We were sent a memorandum from the Director of CDCR to reduce staff as much as possible. Our I.P.O, PII has not done so and is putting our lives in danger of COVID19. We are... See More not social distanced in the office, we are not 6 feet apart and some of us face each other. We have now had 4 positive cases in our small office alone, and we are told to just wipe down the infected persons desk and get back to work. We currently have the means to work from home a couple days a week to reduce exposure but it is not being done in a timely manner or in a manner that we are not at risk. I am so nervous and have anxiety going into that office thinking I will be next or I will take it home to my small child and toddler. Please help us.


Source: Osha.gov | Receipt Date: 2020-12-13
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T8CCR 3205(c)(6)- We have had 5 confirmed cases of Covid-19 out of 12 staff. We are not provided N95 mask, we were not social distanced until today. Even with the division of the team into two rooms there is not enough protection between us. We do not... See More have hot water to wash our hands as advised from the CDC all we have is ICE cold water. Many employees who travel through our halls are not wearing their mask properly,. We are fearful to leave our office for any reason because we are terrified because of the careless reckless behavior we see. With people removing their mask or not wearing them properly. While getting tested we are in a room full of people and have to remove our mask which puts us at risk there is no time allowed between each person being tested. The tables are not always wiped down. There are not hand sanitizers at each main doorway as everyone has to touch those door handles We are setup for teleworking but are denied the ability to do so because CDCR will not allow us access to our required programs at home. We have access but are forbidden to use it and denied teleworking while other departments at CIM have staff that telework 100%.


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Endo International plc announced today that one of its operating companies, Par Pharmaceutical, Inc. (Par), is voluntarily recalling one lot of Treprostinil Injection 20mg/20mL (1mg/mL) to the consumer level. The product is being recalled due to the potential for the presence of silicone particulates in the product... See More solution. The lot was distributed nationwide to wholesalers and hospitals from June 16, 2022, through October 17, 2022. To date, Par has not received any reports of adverse events related to this recall.

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Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to taking or using this drug product.

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: Endo International, Par Pharmaceutical
Brand name: Par Pharmaceutical
Product recalled: Treprostinil 20mg/20mL Injection
Reason for the recall: Potential Presence of Silicone Particulate Matter
FDA Recall date: March 12, 2024

Source: www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/par-pharmaceutical-issues-voluntary-nationwide-recall-one-lot-treprostinil-injection-due-potential
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