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Covid-19 OSHA Complaint, Andrew Electric Company Incorporated, 2102 E Pecan St, Pflugerville, TX 78660, USA

1 year ago

2102 Pecan Street East, Pflugerville, 78660 Texas, United States

Item#1: Social distance is not enforce by the employer. Item#2: Employees are not provided with an area where they can wash their hands with water and soap. Item#3: Employees are working near the edge at the 5th floor (~50 feet high) with no fall protection. Thus, exposing the employees to a fall hazard. Item#4: Employees use boom lifts without body harnesses throughout the jobsite.

Alleged Hazards: 4, Employees Exposed: 15
Source: Osha.gov | Receipt Date: 2020-10-13

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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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Recent Interesting Reports

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
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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
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2 Shares


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
Product Description & Size: Al kanater Tahini Sesame Paste 1 lb. (454 gr)
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.
Brand name: Al Kanater
Product recalled: Tahini
Reason of the recall: Salmonella
FDA Recall date: November 30, 2021

Check the full recall details on fda.gov

Source: FDA
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DreamBone Twist Sticks are making my dogs vomit. They were purchased from Chewy.com.

I have been giving our dogs Dream Sticks with no problem. Three of our dogs started vomiting this morning and two have continued vomiting throughout the day. Our Pyrenees-Lab has vomited six times so... See More far today and STILL pieces of DreamBone Twist Sticks 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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Nutracap Holdings, LLC of Norcross, Georgia is voluntarily recalling various dietary supplements due to undeclared wheat, milk, soy and/or coconut on the labels. People who have an allergy or severe sensitivity to soy, milk, wheat, or coconut run the risk of serious or life-threatening allergic reaction if... See More they consume products containing soy, milk, wheat, or coconut.

On 11/4/2021 during an FDA inspection the firm was notified that their labels failed to disclose the presence of allergens on some of their products. The recalled products were shipped between June 4, 2020 through October 1, 2021 to distributors and retailers in Alabama, California, Florida, and Texas. There have been no illnesses reported to date.

The affected products are:

Brand: Boba Origin. Product: 100% Whey Protein Isolate. Flavor: Brown Sugar Milk, Tea, Undeclared milk, & soy. Size: 1 gallon plastic jar. Lot No. 2106263. Exp. 07/2023

Brand: Etedream. Product: Etegrow ISO. Flavor: Snicker Doodle, Undeclared milk. Size: 2gallon plastic jar. Lot No. 2106002. Exp. 06/2023


Brand: RAW. Product: Vegan Protein Flavor: Peanut Butter, Undeclared coconut. Size: 1gallon plastic jar. Lot No. 2108070, 2104340, 2102018, 2012304, 2010266, 2010102, 2007037/746, 2005132. Exp. 08/2023, 04/2023, 02/2023, 12/2022, 10/2022, 10/2022, 07/2022, 05/2022

Brand: Steel. Product: Veg-Pro Flavor: Cookies & Crème, Undeclared Wheat. Size: 64 ounce plastic jar. Lot No. 2109390, 2104333, 2011260, 2104007/1041, 2105059, 2011260/994. Exp. 09/2023, 04/2023, 11/2022, 04/2023, 05/2023, 11/2022

Brand: Vital Force. Product: PureISO. Flavor: Milk Chocolate, Cocoa, Undeclared milk. Size: 1gallon plastic jar. Lot. No. 2108191. Exp. 09/2023

Brand: Vital Force. Product: PureISO. Flavor: Creamy Peanut, Butter Vanilla, Undeclared milk. Size: 1gallon plastic jar. Lot No. 2109068. Exp. 09/2023

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.

This recall is being made with the knowledge of the Food and Drug Administration.

Company name: Nutracap Holdings, LLC
Brand name: Etedream, Vital Force, Raw, Boba Origin, Steel
Product recalled: Dietary Supplement Protein Powder
Reason of the recall: Undeclared wheat, milk, soy and/or coconut
FDA Recall date: November 09, 2021

Check the full recall details on fda.gov

Source: FDA
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5


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
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282


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
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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
Reason for Announcement: Undeclared Milk
Company Name: Nutracap Holdings, LLC
Brand Name: Multiple brands
Product Description: Dietary Supplements

Check the full recall details on the FDA website: fda.gov

Source: FDA
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