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Covid-19 OSHA Complaint, Crabbe Huson Group Inc, 121 SW Morrison St, Portland, OR 97204, USA

4 weeks ago

121 Southwest Morrison Street, Portland, 97204 Oregon, United States

Serious

Alleged Hazards: 1,
Source: Osha.gov | Receipt Date: 2021-09-02

937


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About 6 minutes after taking second pfizer dose, I began to sweat, blood pressure dropped, nausea set in and almost lost consciousness a couple of times. A nurse and a doctor stayed with me and offered some water. That didn't help ad after about an hour, I... See More was taken by ambulance to emergency room and treated with fluids and anti-nausea feeds. About 5-6 hours later I began to feel better and went home. | Symptoms: Nausea See Less
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SI
anonymous2659
I hope you are going to be ok. How are you feeling now?
1 Reply 1 day ago
DU
anonymous2660
This sounds like allergic reaction and a terrible thing to post on this forum as it enables the narrative that the vaccine “kills/harms” because a TINY fraction of the population has a severe/bad reaction. Your immune system just sounds weak, the simple fact you were given fluids and fully recovered exemplifies that.
People aren’t even reading everything, they read the first part and “oH gOd aRe yOu OkAy” when CLEARLY you are.
-1 Reply 1 day ago
XJ
anonymous2666
sounds like anxiety
-1 Reply 23 hours ago
5L
anonymous2676
What in the actual heck is wrong with the people who are so crazy about these jabs and putting down anyone who has a reaction? I have to believe that they are paid spokespersons or something, like who tells someone their reaction is because they are weak... seriously anonymous2660, people have legitimate reactions and concerns and this is the place to voice them, and yet people like you belittle them, what is that even about?
1 Reply 4 hours ago
XY
anonymous2682
I love all the comments saying it’s anxiety. I know many people with Heart conditions that they will have the rest of their lives. These reactions are not normal.
Reply 4 hours ago
Had the 2nd AZ vaccine and within 10 minutes I went all dizzy and felt really sick and had the shakes. They offered me some water and told me to stay seated for 20 minutes. After that I was able to leave. The next day all of... See More my bones were aching and I felt dizzy and sick with heart palpitations. Day two now and feeling much better. | Symptoms: Dizziness, Body Ache, Shaking See Less
523


When I took my first and second shots made me extremely tired and I had absolutely no energy, didn't even want to take a bath my legs were extremely weak I mean I felt terrible for more than 2 months. And to top it off September 7... See More .I got Covid and almost died. I couldn't stand up.I didn't eat for a week. Nothing tastes good. It was awful. I didn't have any problems with breathing. I don't think I will do the Booster. I told my doctor and he said it was up to Me ! That Covid is terrible. I m check for Covid once a week. See Less
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DU
anonymous2661
please look up how vaccines work before saying “I will not get the booster” there is NOTHING worrying or concerning about your reaction, your immune system responded accordingly. If anything, it sounds like you have a weak immune system to begin with.
-1 Reply 1 day ago
2T
anonymous2680
No breathing problems, but you almost died?.
Reply 4 hours ago

Recent Interesting Reports

Livia Global, Inc announced the recall of two lots of its liquid probiotics, LiviaOne Liquid Probiotics & BioLifePet Liquid Probiotics, due to the possibility of contamination by Pseudomonas aeruginosa, a microorganism that can cause life-threatening infection in immunocompromised individuals. These products are distributed nationwide through Amazon, wholesale,... See More and direct sales from the company’s website.

Pseudomonas aeruginosa is a microorganism found in the environment that, if ingested, can cause life-threatening infection in immunocompromised individuals. P. aeruginosa infections are generally limited to hospital settings.

This recall only affects the following products with the Lot# 001005-1 Best by: 04/2023 & LiviaOne Nasal Probiotics with Lot# 010620-1 Best by 08/2023 with the following ship dates:
- LiviaOne Daily Probiotics 2oz – UPC 030915 107112 Ship dates 04/16/2021 – 08/30/2021 (1067 units)
- LiviaOne Daily Probiotics 4oz – UPC 030915 107167 Ship dates - 07/09/2021 – 08/30/2021 (384 units)
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- LiviaOne Nasal Probiotics 1oz – UPC 030915 107198 Ship dates 04/21/2021 – 05/12/2021 (480 units)
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Lot numbers are located on the side of the bottle and on the bottom of the outer container in which the product is sold. No other lots or ship dates or any other LiviaOne products are affected by this recall.

Company name: Liva Global, Inc.
Brand name: LivaOne and BioLifePet
Product recalled: Probiotics
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FDA Recall date: December 01, 2021

Check the full recall details on fda.gov

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The affected products are used as antiperspirants and hygiene products and are packaged in aerosol cans. See the link below for Product names and UPC codes and images for further descriptions. They are recalling all lots with expiry through September 2023 of the products listed in the link below.

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Nutracap Holdings, LLC of Norcross, Georgia is voluntarily recalling various dietary supplements due to undeclared milk on the labels. People who have an allergy or severe sensitivity to milk run the risk of serious or life-threatening allergic reaction if they consume products containing milk. There have been... See More no illnesses reported to date.

During a recent FDA inspection, the firm was notified that their labels failed to disclose the presence of milk on some of their products.

The recalled products were shipped between January 2020 through November 2021 to distributors and retailers in Arizona, California, Colorado, Florida, Georgia, Idaho, Illinois, Indiana, Kentucky, Louisiana, Minnesota, Nevada, New Jersey, New York, North Carolina, Ohio, and Texas.

The full list of affected products is on the link below.

Lot numbers and expiration dates are found on the bottom of each container.

Retailers and distributors who have received any of these products should check inventory, immediately remove from sale and notify customers who purchased them of the recall. Nutracap will be providing corrective label stickers for product remaining in stock. Affected consumers who have purchased these products are urged to return them to the place of purchase for a full refund or they may discard the product. Your assistance is appreciated and necessary to prevent consumer illness.

Company Announcement Date: November 12, 2021
FDA Publish Date: November 12, 2021
Product Type: Food & Beverages. Allergens
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International Golden Foods, Inc (IGF) of Bensenville, IL is voluntarily recalling certain lot codes of the Al kanater brand tahini because it has the potential to be contaminated with Salmonella, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people... See More and others with weakened immune system. Healthy persons infected with Salmonella often experience fever, diarrhea (which may be bloody), nausea, vomiting and abdominal pain. In rare circumstances, infection with Salmonella can result in the organism getting into the bloodstream and producing more severe illnesses such as arterial infections (i.e., infected aneurysms), endocarditis and arthritis.

The product was distributed nationwide and is sold in 16 Oz. jars. The jars are labelled “Al kanater Tahini.” Lot codes are printed on the jar. Product code, description, lot code, and UPC information are noted below.

Product Code: AT1LB
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Lot #: TT4N‐201127
UPC: 6‐92551‐00002‐0

No illnesses have been reported to-date in connection with the Al Kanater Brand Tahini.

This problem was revealed as a result of a random sampling by the Michigan Department of Agriculture.

Consumers who have purchased Al kanater Tahini with these lot codes should discontinue use and return it to the store of purchase for a full refund. Retailers that may have further distributed the recalled lot codes should share this notice with their customers.

Company name: International Golden Foods, Inc.
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Veklury is indicated for the treatment of adults and pediatric patients ≥ 12 years old and weighing ≥40 kg requiring hospitalization for COVID-19. The lyophilized form of Veklury (remdesivir 100 mg for injection) is distributed in single dose clear glass vials in powder form and reconstituted at the site of use.

Veklury lots 2141001-1A and 2141002-1A were distributed nationwide in the United States, beginning October 2021. NDC, lot, expiration date and distribution dates can be found below.

Product Description: Veklury® (remdesivir 100mg for injection)
NDC: 61958-2901-02
Lot #: 2141001-1A - 2141002-1A
Expiration Date: 01/2024 - 01/2024
Distribution date to wholesalers: 10/25/21-10/26/2021 - 10/26/21-11/02/2021

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