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Round Table Pizza
Updated: February 17, 2021 12:00 PM
2 years ago
3203(a): Employer is not doing contact tracing and are transferring potential COVID-19 infected employees from one store to another. Those employees have not been tested for COVID-19.
Alleged Hazards: 1, Employees Exposed: 1
Source: Osha.gov | Receipt Date: 2020-11-30
Covid-19 OSHA Complaint, Round Table Pizza, 16122 Goldenwest Street, HUNTINGTON BEACH, CA, 92647, USA
2 years ago
T8 CCR § 3203(a)(4)(C) - Three employees who work at another Round Table (at 19750 Beach Boulevard HB) were transferred to this restaurant after an employee tested positive for Covid-19.
Alleged Hazards: 1, Employees Exposed: 8
Source: Osha.gov | Receipt Date: 2020-06-30
3203: Employer not following Covid-19 plan per complaint about employee exposure.
Alleged Hazards: 1, Employees Exposed: 1
Source: Osha.gov | Receipt Date: 2020-11-13
T8 CCR 3203(a)(4)&(6) Employees work in close proximity in the pizza preparation without wearing face coverings.
Source: Osha.gov | Receipt Date: 6/29/2020
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CDC, public health and regulatory officials in several states, and the U.S. Food and Drug Administration Center for Veterinary Medicine (FDA CVM) are investigating a Salmonella Kiambu multistate outbreak linked to Dry Dog Food. As of November 1, 2023, 7 people infected with the outbreak strain of... Salmonella have been reported from seven states (AL, CA, FL, HI, KY, MN, and OK). One person was hospitalized and no deaths have been reported. Illnesses started on dates ranging from January 14, 2023, to August 19, 2023.
People in this outbreak got sick from touching recalled dog food, touching things like dog bowls that contained the dog food, or touching the poop or saliva of dogs that were fed the dog food. Most of the sick people in this outbreak are infants. Epidemiologic and laboratory data show that a specific lot of Victor brand Hi-Pro Plus dry dog food is contaminated with Salmonella and has made people sick. The manufacturer, Mid America Pet Food, has recalled this and all other brands of pet food they make. Investigators are working to identify any additional products that might be contaminated.
On September 3, one lot of Victor brand Hi-Pro Plus dog food was recalled. Affected products: 5-pound bags with lot code 1000016385. Best-by date 4/30/2024.
On October 30, three lots of Victor Super Premium Dog Food, Select Beef Meal & Brown Rice Formula were recalled. Affected products: 5 pound, 15 pound, and 40 pound bags Best-by date 6/12/2024 Lot numbers 1000016890, 1000016891, 1000016892.
On November 9, Mid America Pet Food recalled all brands of pet food they make. Affected products: All dog and cat food, Best by dates before 10/31/2024, Brands include: Victor Super Premium Dog Foods, Wayne Feeds Dog Food, Eagle Mountain Pet food, Member’s Mark. Multiple bag sizes including: 5 pound, 15 pound, 16 pound, 30 pound, 40 pound, and 50 pound.
The CDC advises the following to Pet Owners:
- Throw away recalled pet food in a sealed trash bag and place it in a sealed trash can so that wildlife cannot get to it. Don’t let children touch the recalled pet food. Don’t feed recalled pet food to pets or other animals. Don’t donate recalled pet food.
- Clean surfaces and items, including pet items like bowls, that might have touched the recalled pet food.
- Contact a veterinary care provider if your pet has any of these symptoms after eating the recalled pet food: Vomiting, Diarrhea (may be bloody), Fever, Loss of appetite, Decreased activity level
- Contact a healthcare provider if you or your child have any of these severe Salmonella symptoms: Diarrhea and a fever higher than 102°F, Diarrhea for more than 3 days that is not improving, Bloody diarrhea, So much vomiting that you or your child cannot keep liquids down, Signs of dehydration, such as: Not peeing much, Dry mouth and throat, Feeling dizzy when standing up.
In case you are experiencing Salmonella symptoms such as diarrhea, abdominal cramps, and fever, it is important to report it. It can help to detect & resolve outbreaks early and prevent others from being harmed, and it enables better surveillance. If symptoms persist, seek medical care.
1 week ago
Bayer is voluntarily recalling one lot of Vitrakvi® (larotrectinib) Oral Solution 20 mg/mL in 100mL glass bottles to the consumer/user level. The product is being recalled due to microbial contamination identified as Penicillium brevicompactum observed during routine ongoing stability testing. It was distributed to wholesale distributors and... specialty pharmacies nationwide between January 3, 2023, and February 13, 2023. To date, Bayer has not received any adverse events related to this recall.
Risk Statement: Vitrakvi® is indicated for the treatment of solid tumors that are NTRK gene fusion positive, it is expected that patients on Vitrakvi® may be immunocompromised. Although there is little data in the literature on human pathology caused by Penicillium brevicompactum, there are cases of invasive disease caused by similar Penicillium species, particularly in patients with underlying immunosuppression. Therefore, there is a reasonable probability that ingestion of Penicillium brevicompactum in patients on Vitrakvi® with underlying immunosuppression may result in invasive fungal infections of the blood or pneumonia that can be life-threatening.
The impacted lot of Vitrakvi® is packaged in a 100mL glass bottle with NDC# 50419-392-01 and is identified with Lot# 2114228 and an expiration date of February 29, 2024. Product bottle and carton label images and information on the lot number that falls under this recall is attached
Bayer notified all distributors and pharmacies of this recall on November 8, 2023. Bayer has engaged Qualanex to manage the recall of the product down to the consumer level. Qualanex has notified Vitrakvi® distributors via a recall notification letter and will arrange for the return of the recalled lot from distributors, specialty pharmacies, and consumers.
Consumers who have the recalled Vitrakvi® product should immediately stop use of this particular lot of product and contact their physician or healthcare provider if they have any questions, concerns or have experienced any problems related to Vitrakvi® Oral Solution 20 mg/mL.
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: Bayer
Brand name: Bayer
Product recalled: Vitrakvi® (larotrectinib) Oral Solution 20 mg/mL in 100mL glass bottles
Reason of the recall: Microbial contamination identified as Penicillium brevicompactum
FDA Recall date: November 21, 2023
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