Taco Bell, 1301 S Washington St, Grand Forks, ND 58201, USA

38 employees tested positive for Covid-19 at Target Distribution Center in Linn County. Investigation Start Date: 21-10-2021, with the most recent onset of: 24-11-2021 New Cases of: 38

Source: www.oregon.gov See Less

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18 employees tested positive for Covid-19 at The Home Depot in Marion County. Investigation Start Date: 07-10-2021, with the most recent onset of: 17-11-2021 New Cases of: 18

Source: www.oregon.gov See Less

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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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An employee at Extra Foods, 27th Street, Grand Forks, BC, Canada tested positive for Covid-19. Last work date: May 25

Source: bc.ctvnews.ca See Less

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For employees exposed to health hazards without proper personal protective equipment when cleaning rooms where COVID-19 positive individuals have stayed.

Alleged Hazards: 1, Employees Exposed: 2
Source: Osha.gov | Receipt Date: 2021-01-05 See Less

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1. For employees potentially exposed to COVID-19 infections where a hazard assessment has not been performed that accounts for necessary and required personal protective equipment and administrative controls, to include but not limited to gloves, respirators, aprons/suits, and glasses/face shields. (29 CFR 1910.132, 1910.133, 1910.134, 1910.138) 2.... See More For employees potentially exposed to COVID-19 infections where personal protective equipment is not provided or not appropriate for the work environment. (29 CFR 1910.132, 1910.133, 1910.134, 1910.138) 3. For employees potentially exposed to COVID-19 infections where the employees who test positive with Covid-19 were required to go back to work. 4. For employees potentially exposed to respiratory hazards from mold exposure in the warehouse. [Section (5)(a)(1)]

Alleged Hazards: 4, Employees Exposed: 5
Source: Osha.gov | Receipt Date: 2020-11-19 See Less

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For employees potentially exposed to COVID-19 infections: 1. Where a hazard assessment has not been performed that accounts for necessary and required personal protective equipment to include but not limited to gloves, respirators, aprons/suits, and glasses/face shields. (29 CFR 1910.132, 1910.133, 1910.134, 1910.138) 2. Where personal protective... See More equipment is not provided or not appropriate for the work environment. (29 CFR 1910.132, 1910.133, 1910.134, 1910.138) 3. Where sanitation regarding housekeeping, washing facilities, and toilets are not maintained to prevent the spread of infection. (1910.141)

Alleged Hazards: 3, Employees Exposed: 15
Source: Osha.gov | Receipt Date: 2020-03-12 See Less

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For employees potentially exposed to COVID-19 infections: 1. Where a hazard assessment has not been performed that accounts for necessary and required personal protective equipment and administrative controls, to include but not limited to gloves, respirators, aprons/suits, and glasses/face shields. (29 CFR 1910.132, 1910.133, 1910.134, 1910.138) 2.... See More Where personal protective equipment is not provided or not appropriate for the work environment. (29 CFR 1910.132, 1910.133, 1910.134, 1910.138) 3. Where sanitation regarding housekeeping, washing facilities, and toilets are not maintained to prevent the spread of infection. (29 CFR 1910.141) at or near 3750 32nd Avenue South in Grand Forks, North Dakota.

Alleged Hazards: 3, Employees Exposed: 10
Source: Osha.gov | Receipt Date: 2020-12-07 See Less

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For the employees and donors exposed to Covid-19 where the spread of COVID-19 in not controlled by engineering or administrative controls in accordance with current CDC guidelines at or near 4770 Technology Circle in Grand Forks, North Dakota.

Alleged Hazards: 1, Employees Exposed: 34
Source: Osha.gov |... See More Receipt Date: 2020-12-09 See Less

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For employees potentially exposed to COVID-19 infections: 1. Where a hazard assessment has not been performed that accounts for necessary and required personal protective equipment and administrative controls, to include but not limited to gloves, respirators, aprons/suits, and glasses/face shields. (29 CFR 1910.132, 1910.133, 1910.134, 1910.138) 2.... See More Where personal protective equipment is not provided or not appropriate for the work environment. (29 CFR 1910.132, 1910.133, 1910.134, 1910.138) 3. Where sanitation regarding housekeeping, washing facilities, and toilets are not maintained to prevent the spread of infection. (29 CFR 1910.141) 4. Where employees with confirmed close contact with COVID-19 positive individuals are allowed to work.

Alleged Hazards: 4, Employees Exposed: 30
Source: Osha.gov | Receipt Date: 2020-10-27 See Less

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On 9-24-21 I valued package was returned using Pitney Bowes shipping label provided by the merchant (American Mint). It was dropped off at the USPS store in Daytona Beach, picked up by Daytona Beach Post Office on 9-28-21 and retrieved from that Post office by Newgistics (Pitney... See More Bowes) on 9-30-21. On 10-4-21 it arrived and was dispatched from sorting at the Monroe Township, Middlesex County, New Jersey Post Office. Since then it is missing, in a black hole, unable to be found. This is a shame since this is a product scammed to my mother (senior of 86) who followed every step to have her $149.99 from American Mint and now can not receive her money back since the company has not received the product back. Please address this issue to return what is rightfully my mother's. This is a shame.

Pitney Bowes Returns
Parcel Return Service 56901
Tracking # 4205690192023901007848000000499942 See Less

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On April 6, I ordered a saw for wood and I never received it! See Less

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Nutrisure Ltd is recalling Naturya Hemp Protein Powder because it contains gluten, which is not mentioned on the label. This means the product is a possible health risk for anyone with an allergy or intolerance to gluten. This batch was only sold in Sainsbury’s stores.

Naturya Hemp... See More Protein Powder (100g)
Pack size: 100g
Batch code: W02135
Best before: end of March 2024
Allergens: Gluten

If you have bought the above product and have an allergy or intolerance to gluten, do not eat it. Instead, return it to the store from where it was bought for a full refund.

Company name: Nutrisure Ltd
Product recalled: Naturya Hemp Protein Powder
FSA Recall date: 11/30/2021

Check the full recall details on food.gov.uk

Source: FSA See Less

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Sagent Pharmaceuticals, Inc. on November 19 announced the voluntary nationwide recall of four lots of Levetiracetam Injection, USP, to the user level. The lack of container closure integrity, found in reserve sample vials may result in a non-sterile product.

Risk Statement: Intravenous administration of a product intended... See More to be sterile that is not sterile could result in serious systemic infections which may be life-threatening. 

To date, Sagent has not received reports of any product complaints or adverse events associated with this issue. Levetiracetam Injection, USP 500 mg per 5 mL, is used in the treatment of certain types of seizures and is packaged in a 5mL single-does vial. The Levetiracetam Injection, USP, label and affected lot numbers with Expiration Dates and NDC number can be found in the table below. 

Product: Levetiracetam Injection, USP / Lot Number: B0G85VB /Expiration Date: Jun-2022 / NDC Number: 25021-780-05 / Distribution Dates: May 2021 - August 2021.

Product: Levetiracetam Injection, USP / Lot Number: B0K88VA /Expiration Date: Sep-2022 / NDC Number: 25021-780-05 / Distribution Dates: March 2021 - November 2021.

Product: Levetiracetam Injection, USP / Lot Number: B0K89VA /Expiration Date: Sep-2022 / NDC Number: 25021-780-05 / Distribution Dates: August 2021 - November 2021.

Product: Levetiracetam Injection, USP / Lot Number: B1G194A /Expiration Date: Jun-2023 / NDC Number: 25021-780-05 / Distribution Dates: October 2021.

The product was distributed Nationwide from March to November  2021.

Company name: Sagent Pharmaceuticals, Inc.
Brand name: Sagent
Product recalled: Levetiracetam Injection
Reason of the recall: Lack of sterility assurance
FDA Recall date: November 22, 2021

Check the full recall details on fda.gov

Source: FDA See Less

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Usually is fine. Not this time. I decided to burn Nag Champa incense to meditate. As I was meditating, our dog started sniffling and then began throwing up large amounts of mucous. Her lips were swollen and pulled back slightly. She is ok now, but I've never... See More experienced anything like this using incense before this happened. I often use it for meditation. I called the vet who confirmed this is an allergic reaction and they informed me to monitor her and ensure she is safeand healthy, not vomiting anymore. They instructed me to open all the windows and doors, turn on ceiling fans,and run the furnace heat to pull remaining particulate into the HEPA filter on the furnace and then to replace the filter tomorrow to ensure it doesn't just recirculate the particulate if any happens to get through. Also said to wash hard surfaces in the room it was burned on and vacuum up any furniture,carpet, or rugs there to remove any settled particulate. I'm not sure what went wrong here. I've never had this happen with her or any other dog when burning this.

But even I am sniffling and nauseous after having burned it and my throat is sore. I took benedryl to
prevent an attack in me personally.

Product:
Nag Champa incense sticks.
Label information: Nag Champa Agarbatti Satya Sai Baba. Mfrs. Shrinivas
Sugandhalaya(BNG)LLP.1/9,8th Cross, Magadi Road, Bengaluru-560023, India. Certified green
product. Export Quality.2021 Series. Hand Rolled in India. UPC 8904245400491.Warning: insist for this label to avoid imitation buy from reputed dealers only. Earth. Contains seals with hologram over each side of the box with official logo. NetWt.40g. Quality assurance labels are not actual stickers demonstrating actual checks, but are instead printed onto the package to appear as if they were actual quality assurance stickers and are offset with a white background to trick a consumer. There are three which areas follows. Fake QA sticker1: Quality Assurance Management ISO 9001(check mark symbol)
Fake QA sticker2: Environmental Management ISO 14001(check mark symbol) Fake QA sticker 3: Occupational Health &
Safety OHSAS 45001 (check mark symbol).
Customer care number+917022000111

Item purchased at Archimage. Not their fault. They only buy reputable authentic items and this has to be a bad or contaminated batch here. | Symptoms: Nausea, Other See Less

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I have been applying since the beginning of the month I went to two different appointments and every three hours the system messes up and thinks that I haven’t done my steps See Less

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Mountain Meadow Herbs of Somers, MT is recalling 54 bottles (total 240 capsules per bottle) of Mountain Meadow Herbs brand Candida Flush, Lot# 0120011Q. Some bottles from this Lot have become pressurized over time in storage. When opened, the product may forcefully expel air as well as... See More portions of capsules and powder. This may result in customers sustaining injuries to their hands and eyes, which may require medical attention.

Product was distributed to retailers in IN, MN, MT, NY, TN and in Ontario of Canada.
Product was sold directly to consumers in IN, KY, MN, MO, MT, NE, OH, PA, VA, and WI. The affected Candida Flush has the UPC 8 13086 01593 2, Lot #012001l Q, Exp 12/22.

No illnesses or serious injuries have been reported to date. The recall was the result of an internal investigation stemming from a customer complaint which revealed that the finished products were becoming pressurized over time.

This recall is being made with the knowledge of the U.S. Food and Drug Administration. If you have any of these products, please dispose of them immediately.

Company name: Mountain Meadow Herbs
Brand name: Mountain Meadow Herbs
Product recalled: Candida Flush
Reason of the recall: Due to exploding bottle risk
FDA Recall date: November 17, 2021

Check the full recall details on fda.gov

Source: FDA See Less

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Package was supposed to be delivered November 6, 2021.
After days of endless calls finally told it left teterboro post office November 5 but was never delivered or tracked since. See Less

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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)
- LiviaOne Topical Spray Probiotics 4oz – UPC 030915 107105 Ship dates 07/08/2021 – 07/30/2021 (571 units)
- LiviaOne Nasal Probiotics 1oz – UPC 030915 107198 Ship dates 04/21/2021 – 05/12/2021 (480 units)
- LiviaOne Nasal Probiotics 1 oz - UPC 030915 107198 Ship dates 07/14/2021 – 08/24/2021 (600 units)
- LiviaOne Nasal Probiotics 1 oz – Lot# 010620-1 UPC 030915 107198 Ship dates 10/27/2021 – 11/25/2021 (50 units)
- BioLifePet Probiotics for Cats – UPC 030915 107044 Ship dates 05/05/2021 – 07/26/2021 (128 units)
- BioLifePet Probiotics for Dogs – UPC 030915 107037 Ship dates 05/05/2021 – 08/25/2021 (128 units)

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
Reason of the recall: Pseudomonas aeruginosa
FDA Recall date: December 01, 2021

Check the full recall details on fda.gov

Source: FDA See Less

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I shipped Priority Express on Nov 15 to Essex Junction, VT and after two days it is still showing arrived at Teterboro Distribution Center, Industrial Avenue, Teterboro, NJ, USA on 11/15/2021 at 9:22pm. It should be delivered by Nov 16 at VT See Less

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