Covid-19 OSHA Complaint, Ralco Holdings, 8505 W Doe Ave, VISALIA, CA, 93291, USA

February 3, 2021 12:00 PM

8505 West Doe Avenue, Visalia, 93291 California, United States

1. GISO §3203(a)(3): Employee doing temperature screening in the morning does not wear a face cover. 2. GISO §3203(a)(4): Shared equipment are not being sanitized between shifts. 3. GISO §3203(a)(4): Employees are not provided with a sufficient amount of face covers. 4. GISO §3203(a)(4): Hand sanitizer dispensers are empty. 5. GISO §3366(b): Restrooms are unsanitary. 6. GISO §3366(d): Restrooms do not have hand soap.


Source: Osha.gov | Receipt Date: 2020-07-08

March 1, 2021 12:00 PM

“8 employees at Adlai E. Stevenson School No. 29 located on Kirkland Rd in Rochester recently tested positive for Covid-19.

Source: rochesterfirst.com See Less”

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“33 employees at K11 MUSEA Hong Kong located on Tsim Sha Tsui in Salisbury Rd recently tested positive for Covid-19.

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“An employee at Nestico's located on North Main Street in North Syracuse recently tested positive for Covid-19.

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“An employee at Thai Kitchen Restaurant located on 11 Cumberland St S in Thunder Bay recently tested positive for Covid-19.

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“An employee at McDonald's located on 22780 Lougheed Hwy in Maple Ridge recently tested positive for Covid-19.

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March 1, 2021 12:00 PM

“An employee at McDonald's located on 815 McBride Blvd in New Westminster recently tested positive for Covid-19.

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March 1, 2021 12:00 PM

“An employee at McDonald's located on 1131 Austin Ave in Coquitlam recently tested positive for Covid-19.

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March 1, 2021 12:00 PM

“An employee at T&T Supermarket located on E 1st Ave in Vancouver recently tested positive for Covid-19.

Source: vancouverisawesome.com See Less”

March 1, 2021 12:00 PM

“An employee at T&T Supermarket located on Keefer Pl in Vancouver recently tested positive for Covid-19.

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March 1, 2021 12:00 PM

“An employee at 10 Acres Cafe & Market located on Seaport Pl in Sidney recently tested positive for Covid-19 and passed away.

Source: victoriabuzz.com See Less”

February 10, 2021 6:03 PM

“On 1/20/21 I ordered the little battery chainsaw which is advertised on Facebook all the time. It cost $37.98. I only got a chainsaw blade today. See Less”

February 16, 2021 11:55 PM

“The FSA announced the recall of Boots Multivitamins supplements by Boots because they have been incorrectly packed with multivitamins containing iron. This resulted in vitamin K not being present within the supplement and iron incorrectly added to the supplements instead. Iron has not been mentioned... See Moreon the label. This means the product is a possible health risk to individuals who may also be consuming iron supplements in addition to these multivitamins.

FSA advises consumers to stop taking the multivitamin supplements. Instead, return it to the Boots store from where it was bought for a full refund. This recall affects multivitamins sold between 12 and 19 January 2021 only.

- Boots Multivitamins (180 tablets). Item code: 80 57 311. Batch code: 1805 and 1806. Best before: end of November 2022.

This product does not contain vitamin K but does contain iron. Excess supplemental iron can result in gastrointestinal effects such as pain, discomfort, constipation or nausea and vomiting.

Check the full recall details on the FSA website food.gov.uk See Less”

February 11, 2021 11:05 AM

“Dont order any thing from black cass or funny 456 both r scams i order two saws and got two chains thats it i order a fold up scooter from funny456 and got a charger to what i do not know both arw full of crap and iam out money See Less”

February 12, 2021 3:09 PM

“Blackcass, 2020 Hot Selling-GTA 26 Battery-Powerd Wood Cutter is what I ordered- said it was a stihl model- including case- did not recieve that- have an off brand no case :(not stihl gta-26 model See Less”

February 3, 2021 1:00 PM

“Company name: Apotex Corp
Brand name: Apotex Corp.
Product recalled: Enoxaparin Sodium Injection, USP
Reason of the recall: Packaging error resulting in incorrect dosage listed
FDA Recall date: February 03, 2021
Recall details: Apotex Corp is voluntarily recalling two (2) batches of Enoxaparin... See MoreSodium Injection, USP to consumer level due to a packaging error resulting in some syringes barrels containing 150 mg/mL markings (corresponding to 120 mg/0.8mL strength) instead of 100 mg/mL markings (corresponding to 100 mg/mL strength) on the syringe barrel and vice versa. The packaging error was discovered during a customer complaint investigation. To date, Apotex has not received any reports of adverse events related to use of these two batches. The affected product is manufactured by Gland Pharma Limited, Hyderabad, India.

Health Hazard Assessment: Incorrect syringe barrel marking could lead to miscalculation and inaccurate dose administration to patients. In one recalled batch (batch CS008, strength 100 mg/mL), if a consumer used a 150 mg/mL concentration packaged in a barrel corresponding to a l00 mg/mL concentration, patients could receive 3.75 mg of Enoxaparin, instead of 3 mg of Enoxaparin. In another recalled batch (batch CT003, strength 120 mg/0.8mL), if a consumer used a 100 mg/mL concentration packaged in a barrel corresponding to a 150 mg/mL concentration, patients would receive 2 mg of Enoxaparin rather than 2.5 mg of Enoxaparin. Accidental overdosage following administration of enoxaparin sodium injection may lead to bleeding complications. Alternative, if the dose administered is less than prescribed, the patient may be subject to developing some blood clotting conditions.

Enoxaparin Sodium injection is indicated for the prophylaxis of deep vein thrombosis (DVT), which may lead to pulmonary embolism (PE), Treatment of Acute Deep Vein Thrombosis, prophylaxis of ischemic complications of unstable angina and non-Q-wave myocardial infarction, when concurrently administered with aspirin and Treatment of Acute ST-Segment Elevation Myocardial Infarction.

The affected Enoxaparin Sodium Injection, USP can be identified by NDC numbers stated on carton and label of the product.

Product: Enoxaparin Sodium Injection, USP
Batch #: CS008
Strength: 100 mg/mL
Syringe Barrel Measurement Markings: 100 mg/mL
Pack Size: 10 x 1mL Single Dose Syringes
NDC NumberOn Carton: 60505-0795-4
NDC Number On label: 60505-0795-1
UPC Code on Carton: 360505079544
UPC Code on label: (01)10360505079510

Product: Enoxaparin Sodium Injection, USP
Batch # : CT003
Strength: 120 mg/0.8mL
Syringe Barrel Measurement Markings: 150 mg/ mL
Pack Size: 10 x 0.8 mL Single Dose Syringes
NDC NumberOn Carton: 60505-0796-4
NDC Number On label: 60505-0796-0
UPC Code on Carton: 360505079643
UPC Code on label: (01)10360505079602

The two (2) affected batches of Enoxaparin Sodium Injection, USP were distributed by Apotex nationwide in the USA to Wholesalers and Warehousing Chains. Apotex Corp. is currently notifying its affected direct account Wholesalers and Warehousing Chains, via mail (FedEx Standard Overnight) by mailing a recall notification letter and is arranging for return of all recalled product.

Check the full recall details on fda.gov

Source: FDA See Less”

March 3, 2021 4:00 PM

“Company name: Bravo Packing, Inc.
Brand name: Bravo Packing, Inc.
Product recalled: Ground Beef and Performance Dog, frozen raw pet food
Reason of the recall: Potential for Salmonella and Listeria monocytogenes
FDA Recall date: March 03, 2021
Recall details: Company Announcement Bravo Packing,... See MoreInc. of Carneys Point, NJ is recalling all Ground Beef and Performance Dog, a frozen raw pet food because it has the potential to be contaminated with Salmonella and Listeria monocytogenes. Salmonella can cause illness in animals eating the products, as well as people who handle contaminated pet products, especially if they have not thoroughly washed their hands after having contact with the products, infected animals or any surfaces exposed to these products.  Listeria monocytogenes is an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, server headache, stiffness, nausea, abdominal pain and diarrhea, Listeria monocytogenes infection can cause miscarriages and stillbirths among pregnant women. Healthy people infected with Salmonella should monitor themselves for some or all of the following symptoms: nausea, vomiting, diarrhea or bloody diarrhea, abdominal cramping and fever. Rarely, Salmonella can result in more serious ailments, including arterial infections, endocarditis (an infection of the heart muscle), arthritis, muscle pain, eye irritation and urinary tract symptoms. People who have these symptoms after having contact with this product or an animal that has eaten this product should contact their healthcare providers. Pets with Salmonella infections may be lethargic and have diarrhea or bloody diarrhea, fever, and vomiting. Some pets will have decreased appetite, fever and abdominal pain. Pets exposed to contaminated food can be infected without showing symptoms. If your pet has consumed the recalled product and has these symptoms, please contact your veterinarian. Infected animals including those without symptoms, can also shed Salmonella through their feces and saliva, spreading pathogens into the home environment and to humans and other animals in the household. No human or animal illnesses have been reported to date. Bravo Packing, Inc. is voluntarily recalling the products after samples of Performance Dog and a sample of Ground Beef were collected during an FDA inspection, tested positive for Salmonella and Listeria monocytogenes. Performance Dog generally works with the distributor located in Brooklyn, New York, that fills orders to brick-and-mortar retail stores or to consumers directly nationwide. Performance Dog and Ground Beef both come frozen in 2-pound and 5-pound plastic sleeves. If you have an Ground Beef or Performance Dog, please throw it away. Consumers with questions should contact Bravo Packing, Inc. at 856-299-1044 (Monday – Friday, 9:00AM-2:00PM, EST).
Check the full recall details on fda.gov
Source: FDA See Less”

February 21, 2021 9:27 AM

“I received the 2nd covid 19 vaccine shot from Pfizer at the Amazon site February 20th at 1:00 p.m..
I have a mildly sore right shoulder and no other symptoms. See Less”

February 22, 2021 11:20 PM

“I order the 2020 GTA-26 Battery powered wood cutter which they advertise at a price of $29.99. What arrived in the mail was a chain with two cloth handle, which I didn't order. They refuse to refund me or give me a return address. This is what i got in response to my request for a refund.

Pony... See MoreGreen （shenlantiaodong）
2021年2月22日 GMT+817:59
Dear customer,
Sorry to hear that you did not satisfy with the item you received.
If you would like to get the chainsaw, we may offer a discount for you to get the one you actually need.
We can make an exception for you with a surcharge $60, and you will get the chainsaw which costs $89.99. It's equivalent to you buying the chain for free. The chain you received before can be used as a simple tool as a free gift from us."

They are a complete scam See Less”

February 21, 2021 7:00 PM

“I ordered a battery operated mini chainsaw. They sent me a chain with a strap on each end. After many emails they told me that I did order it. No, I didn’t. 5 shoulders, I wouldn’t have. I looked them up and that is when I started finding the reports. See Less”

February 11, 2021 6:25 PM

“I did very well with my first shot of Moderna. I had no reaction except a very sore arm at the injection sight. See Less”