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IMPORTANT - YOUR REPORT IS QUEUED - IT MAY TAKE UP TO 12 HOURS FOR YOUR REPORT TO SHOW ON OUR HOME PAGE (IF NOT OPTED AS PRIVATE)

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Covid-19 OSHA Complaint, George Hackney, Inc., 130 N Virginia Street, QUINCY, FL, 32351, USA

February 2, 2021 12:00 PM

130 North Virginia Street, Quincy, 32351 Florida, United States

a. In the Vegetation Room, employees watering the trays are exposed to 30 feet fall hazard in that the anchor points used to tie off are unsafe. b. In the vegetation room, employees are exposed to struck-by and fall hazards in that the trays that are on each landing are not adequately supported. The rack system is made of thin plastic and overloaded. c. Employees are exposed to Covid-19 due to lack of enforcement of social distancing guidelines.


Source: Osha.gov | Receipt Date: 2020-11-17

Reported By SafelyHQ.com User

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“1. Employees who have tested positive for COVID-19 have been permitted to come to work. The employer did not follow Pennsylvania Department of Health and Centers for Disease Control and Prevention (CDC) guidelines for informing employees of their possible exposure to COVID-19 in the workplace. 2. An... See Moreemployee who was working at the facility tested positive for COVID, was hospitalized and has since died. The employer has not taken any steps to sanitize the facility in order to protect workers who remain in the department(s) where the employee worked and/or traveled in the course of the work day. 2. Employees are not wearing face coverings in accordance with Pennsylvania Department of Health and Centers for Disease Control and Prevention (CDC) guidelines and the employer is not enforcing the use of face masks.

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“1. Pallets in the racking system are stored in an unsafe manner in that they are not wrapped, putting product at risk of falling on employees. 2. Product is staged in walk ways, creating a trip and fall hazard. 3. The employer has not implemented social distancing for infection control.

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“a. In the Vegetation Room, employees watering the trays are exposed to 30 feet fall hazard in that the anchor points used to tie off are unsafe. b. In the vegetation room, employees are exposed to struck-by and fall hazards in that the trays that are on each landing are not adequately supported. The... See Morerack system is made of thin plastic and overloaded. c. Employees are exposed to Covid-19 due to lack of enforcement of social distancing guidelines.


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February 2, 2021 12:00 PM

“a. In the Vegetation Room, employees watering the trays are exposed to 30 feet fall hazard in that the anchor points used to tie off are unsafe. b. In the vegetation room, employees are exposed to struck-by and fall hazards in that the trays that are on each landing are not adequately supported. The... See Morerack system is made of thin plastic and overloaded. c. Employees are exposed to Covid-19 due to lack of enforcement of social distancing guidelines.


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Recent Interesting Reports

February 10, 2021 6:03 PM

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January 29, 2021 10:45 AM

“The U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) is issuing a public health alert for ready-to-eat (RTE) beef jerky products due to misbranding and an undeclared allergen. The product may contain anchovies, a known allergen, which is not declared on the product label. F... See MoreSIS is issuing this public health alert out of the utmost of caution to ensure that consumers with allergic reactions to anchovies are aware that these products should not be consumed. This is a health hazard situation where there is a remote probability of adverse health consequences from the use of the product because of the presence in a product of very small amounts of the undeclared allergens are typically associated with milder human reactions. A recall was not requested because the products are not currently available for sale to consumers.

The RTE beef jerky products were produced from October 20, 2020 through January 12, 2021 and have a one-year shelf life. The product labeled as “CHARLIE BROWN FARMS PREMIUM BEEF JERKY Original Prime Rib” contains Worcestershire, which is not listed as an ingredient, but was utilized in the product formulation. The following products are subject to the public health alert: [View Labels (PDF only)]

3-oz., 4-oz. and 8-oz. gold foil bags of “SETTLERS JERKY PEPPERED BEEF
3-oz., 4-oz. and 8-oz. gold foil bags of “SETTLERS JERKY OLD FASHIONED”
4-oz. gold foil bags of “SETTLERS JERKY HOT BEEF
3-oz., 4-oz. and 8-oz. gold foil bags of “SETTLERS JERKY PRIME RIB”
3-oz., 4-oz. and 8-oz. gold foil bags of “SETTLERS JERKY RING OF FIRE BEEF JERKY”
3-oz., 4-oz. and 8-oz. gold foil bags of “SETTLERS JERKY GHOST PEPPER
3.25-oz. silver bags of “Sierra Madre Provision Co. OLD FASHIONED BEEF JERKY”
3.25-oz. silver bags of “Sierra Madre Provision Co. PEPPERED BEEF JERKY”
3.25-oz. silver bags of “Sierra Madre Provision Co. HOT BEEF JERKY”
3.25-oz. silver bags of “Sierra Madre Provision Co. GHOST PEPPER BEEF JERKY”
3.25-oz. silver bags of “Sierra Madre Provision Co. RING OF FIRE BEEF JERKY”
3-oz., 4-oz. and 8-oz. silver bags of “CHARLIE BROWN FARMS PREMIUM FRESH BEEF JERKY GHOST PEPPER
3-oz. and 4-oz. gold bags of “CHARLIE BROWN FARMS PREMIUM FRESH BEEF JERKY Original Prime Rib”
3-oz. and 4-oz. gold bags of “CHARLIE BROWN FARMS PREMIUM FRESH BEEF JERKY RING OF FIRE”
The products bear establishment number “EST. 8275” inside the USDA mark of inspection. These items were distributed for wholesale and also sent to retail locations in California.

FSIS is concerned that some product may be in consumers’ pantries.

The problem was discovered by FSIS inspection personnel. There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about an illness should contact a health care provider.

Consumers with food allergies who have purchased these products are urged not to consume them. These products should be thrown away.

For more info: fsis.usda.gov

Source: FSIS
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2nd Pfizer vaccine, Seattle, WA, USA

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“I received the 2nd covid 19 vaccine shot from Pfizer at the Amazon site February 20th at 1:00 p.m..
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February 17, 2021 6:09 PM

“A scam regarding a small knock-off chain saw that is the center of a scam by Blackcass of Houston, TX or LA, CA or probably China somewhere. We ordered a Blackcass 2020 Hot selling GTA 26 Battery-Powered Wood Cutter X 1 in December 2020. We did received, via USPS, a 25" long segment of chain saw l... See Moreinks with Orange handles on each end, so it is NOT Battery-Operated. One of the photos in the Blackcass ad that are associated with this SCAM are EXACTLY the same photo used by the very legitimate Stihl company model GTA-26...only the word, "Stihl" is omitted on the Blackcass ad's photo. So, consumers and the real manufacturer are BOTH being scammed. See Less
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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
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February 15, 2021 1:00 AM

“I ordered 2 chainsaws from an ad on the internet which popped up while playing cards on my phone from a web company called Blackcass.com. I thought that I was ordering rechargable woodcutter/chainsaws, but received two chains instead. They would not refund my money or allow me to return and get a re... See Morefund. They said that I had ordered the chains when I only see a big picture of a chainsaw. Their website is misleading to say the least. I would say I was scammed. They also scam people on their website with another chainsaw they are selling that has the well known brand name of Stihl on the saw. Then they send you an off brand saw made in China. Fraud indeed! See Less
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January 29, 2021 10:47 AM

“Alternative Foods London Ltd is recalling OGGS Zesty Lemon Cake because it contains soya that is not declared on the label. This means the product is a possible health risk for anyone with an allergy to soya.

Product details
OGGS Zesty Lemon Cake
Pack size 386g
Best before 26 January 2021; 02... See MoreFebruary 2021; 09 February 2021 and 16 February 2021
Allergens Soya
Risk statement
Allergen(s): Soya

This product contains soya making the product a possible health risk for anyone with an allergy to soya.

Alternative Foods London Ltd is recalling the above product from customers and has contacted the relevant allergy support organisations, which will tell their members about the recall. The company has also issued a point-of-sale notice to its customers. These notices explain to customers why the product is being recalled and tell them what to do if they have bought the product. Please see the attached notice.

If you have bought the above product and have an allergy to soya, do not eat it. Instead return it to the store which you purchased it for a refund.

Check the full recall details on food.gov.uk

Source: FSA
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Reported By SafelyHQ.com User

January 29, 2021 10:45 AM

“The U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) is issuing a public health alert for approximately 43 pounds of not-ready-to-eat (NRTE), heat treated, not fully cooked chicken enchilada products due to misbranding and an undeclared allergen. FSIS is issuing this public... See Morehealth alert out of the utmost of caution to ensure that consumers with allergic reactions to soy are aware that these products should not be consumed. A recall was not requested because the chicken enchilada products are no longer available in commerce.

The NRTE product labeled as “HyVee mealtime CHICKEN ENCHILADAS” was produced on Jan. 3, 2021. The following product is subject to the public health alert: [View Label (PDF only)]

62.4-oz. (3-lbs. 14.4-oz.) heat and serve container of “HyVee mealtime CHICKEN ENCHILADAS” with lot code “21003” and “Best If Use By: 01/10/2021” date on the product label. The products bear establishment number “P51558” inside the USDA mark of inspection. These items were distributed to HyVee retail locations in Illinois, Iowa, Kansas, Minnesota, Missouri, Nebraska, South Dakota and Wisconsin.

The problem was discovered when a HyVee retail store employee identified the labeling issue and reported it to the establishment.

FSIS is concerned that some product may be in consumers’ refrigerators or freezers. Consumers with food allergies who have purchased these products are urged not to consume them. These products should be thrown away.

There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about an illness should contact a health care provider.

For more info: fsis.usda.gov

Source: FSIS
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Reported By SafelyHQ.com User

February 11, 2021 5:22 PM

“Got my second Moderna Covid-19 vaccine shot, no side effects this time. A little tired and thirsty but so far so good. See Less
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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
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