Product: Meat

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The Norton Sound Health Corporation (NSHC) Office of Environmental Health is urging residents in the area to ensure their pets receive rabies vaccinations following a positive rabies test in a moose in Teller. Several community members in Teller reported an aggressive moose on June 2, displaying behaviors … See More
consistent with rabies. The Alaska Department of Fish & Game (ADF&G) promptly responded to the situation and subsequent tests confirmed the presence of rabies in the moose.

This incident marks the first recorded case of rabies in moose in Alaska. The detected virus strain matches the variant recently found in red foxes, leading experts at ADF&G to speculate that the moose was likely infected by a fox. ADF&G has announced plans to intensify rabies surveillance efforts. They will be conducting tests on brain samples from deceased or euthanized wild mammals in regions with endemic fox rabies, including Western Alaska, whenever feasible. This decision aims to enhance early detection and control measures for the disease, as stated in a recent ADF&G press release.

ADF&G encourages individuals who encounter a dead mammal or witness a mammal displaying signs of rabies to immediately report their sighting to the department. Symptoms of rabies include sudden behavioral changes, such as staggering, aggression, fatigue, excessive drooling, uncoordinated movements, self-biting, chasing vehicles, or disorientation. While capturing photographic or video evidence of the animal can assist in evaluation, it is crucial to prioritize personal safety by maintaining a safe distance to avoid potential exposure.

According to the state wildlife veterinarian at ADF&G, moose displaying normal behavior are considered safe for consumption. However, it is advisable to take precautions when harvesting any mammal. This includes the use of rubber or latex gloves, thorough handwashing after handling the animal, and disinfection of any equipment used during the process. Hunters and trappers should refrain from eating, drinking, or smoking until they have properly sanitized their hands. Furthermore, the meat should be cooked to an internal temperature of 165 degrees F before consumption to ensure safety.

Alicia Reitz, OEH Specialist, emphasizes that vaccinating dogs and cats is the most effective means of protecting individuals from the rabies virus. Additionally, she highlights the importance of restraining dogs to minimize potential interactions with foxes and other wildlife. It is equally vital to limit foxes' access to garbage or other attractants. These preventive measures play a crucial role in reducing the risk of exposure.

It is recommended that all dogs and cats receive rabies vaccinations at three months of age, with a booster shot one year later, and subsequent revaccinations every three years. Vaccines are available free of charge through the Lay Vaccinator program administered by OEH.

In the event of fox-human interactions resulting in wounds, immediate washing with soap and water is crucial, followed by prompt medical attention. If any deceased mammals are discovered or put down, it is essential to reach out to Fish and Game or OEH to facilitate proper testing.

By staying vigilant, maintaining pet vaccinations, and following recommended precautions, residents can help mitigate the risks associated with rabies and ensure the well-being of both their pets and the community.

Source: www.nortonsoundhealth.org/press-release-teller-moose-tests-positive-for-rabies/
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#teller #alaska #us

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I got ads from a page of crazy offers just yesterday, June 10, 2023. I thought it could be a scam or a scam. since the minimum purchase for free shipping is 32€, I bought 36. I authorized the payment but still, I was left with the … See More
fly behind my ear. Unfortunately, I researched the company name and this page pops up. I notified the Spanish national police online, block my card. From Everything is learned.

_Company Name_ FADEL-BEATTY LIMITED Company Address_ SUITE 10542, BALMORAL INDUSTRIAL ESTATE, ABBEYLANDS, NAVAN MEATH, C15 DD72, IRELAND (This is not a return address) Email_ tessavo@vlkpkg.com
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#scam #onlineshopping #onlinescam #delivery #navan #countymeath #ie

Ascend Laboratories LLC. is voluntarily recalling Dabigatran Etcxilate Capsules. USP 75 mg and 150 mg to the consumer/user level due to the presence of a nitrosamine. N-nitroso-dabigatran, above the established Acceptable Daily Intake (ADI) level. The product lots were distributed nationwide to wholesalers, Distributors and Retailers (dispensers) … See More
in the United States from June 2022 to October 2022. To date, Ascend Laboratories LLC., has not received any reports of adverse events related to this recall.

Nitrosamines are common in water and foods, including cured and grilled meats, dairy products and vegetables. Everyone is exposed to some level of nitrosamines. These impurities may increase the risk of cancer if people are exposed to them above acceptable levels over long periods of time. The product is used as an oral anticoagulant to lower the risk of stroke and blood clots.

The NDC. Lot Number. Expiration Date. and Packaging Configuration details for Dabigatran Etexilate Capsules that are subjected to this recall are shown in the image below.

In case you experience harm from these products, it is important to report it. It can help to detect & resolve issues and prevent others from being harmed, and it enables better surveillance. If symptoms persist, seek medical care.

Company name: Ascend Laboratories LLC.
Brand name: Ascend Laboratories
Product recalled: Dabigatran Etexilate Capsules, USP
Reason of the recall: Detection of N-Nitrosodimethylamine (NDMA) Impurity
FDA Recall date: March 22, 2023

Source: www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/ascend-laboratories-llc-issues-voluntary-nationwide-recall-dabigatran-etexilate-capsules-usp-75-mg
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#blood #drugs #us

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I was working there and only last a couple weeks. The filth. I’ve never seen a place of business especially one where food is being handled. In the far back cooler the is raw meet over cooked meat. The amount of rotting blood on the floor was so gross. And owner does not care

#blood #raw #cleanliness #foodsafetyissue #510mainstreet #humboldt #saskatchewan #ca

Lupin Pharmaceuticals Inc. is voluntarily recalling four (4) lots of Quinapril Tablets to the patient (consumer/user) level due to the presence of a nitrosamine impurity, N-Nitroso-Quinapril, observed in recent testing above the Acceptable Daily Intake (ADI) level. To date, Lupin has received no reports of illness that … See More
appear to relate to this issue. Lupin discontinued the marketing of Quinapril tablets in September 2022. It was distributed nationwide in the US to wholesalers, drug chains, mail-order pharmacies, and supermarkets.

Nitrosamines are common in water and foods, including cured and grilled meats, dairy products, and vegetables. Everyone is exposed to some level of nitrosamines. These impurities may increase the risk of cancer if people are exposed to them above acceptable levels over long periods of time. Quinapril tablet USP is an angiotensin-converting enzyme (ACE) inhibitor indicated for the treatment of hypertension, to lower blood pressure. Lowering blood pressure reduces the risk of fatal and nonfatal cardiovascular events, primarily strokes and myocardial infarctions.

Quinapril Tablets USP 20mg, and 40mg is packaged in 90 count bottles. The recalled lots are included in the table below:

Product: Quinapril Tablets USP, 20mg
Lot No: G102929
Expiry: 04/2023
NDC: 68180-558-09 (90’s)
UPC: 368180558095
Distribution Dates: 03/15/2021 – 09/01/2022

Product: Quinapril Tablets USP, 40mg
Lot No: G100534, G203071, G100533
Expiry: 12/2022, 12/2022, 03/2024
NDC: 68180-554-09 (90’s)
UPC: 368180554097
Distribution Dates: 03/15/2021 – 09/01/2022

Lupin Pharmaceuticals Inc. is notifying its wholesalers, distributors, drug chains, mail order pharmacies and supermarkets by phone and through recall notification and is arranging for the return of all the recalled product lots.

Patients taking, Quinapril Tablets USP, 20mg, and 40mg are advised to continue taking their medication and contact their pharmacist, physician, or medical provider for advice regarding an alternative treatment.

Wholesalers, distributors and retailers that have Quinapril Tablets USP, 20mg, and 40mg that are being recalled should discontinue distribution of the recalled product lots immediately.

This recall is being conducted with the knowledge of the U.S. Food and Drug Administration.

Company name: Lupin Pharmaceuticals Inc.
Brand name: Lupin
Product recalled: Quinapril 20 and 40 mg tablets
Reason of the recall: Presence of nitrosamine impurity, N-Nitroso-Quinapril
FDA Recall date: December 21, 2022

Source: www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/lupin-pharmaceuticals-inc-issues-voluntary-nationwide-recall-four-lots-quinapril-tablets-due
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#blood #drugs #us #vegetable #meat #ro-tel

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user-zgmd4659

These thieves just sent me one of those feathered pens (dolin youpin 1502 Worlds Map Series). I reported it to my bank and now I am reporting it to the Las Vegas Police which I recommend everybody does. The bastards have a website to sell stuff, like ink for this pen , but Ill buy my ink from Office Depot. There has to be a way to shut these bastards down. Let's do it together.

East Windsor, New Jersey, Aurobindo Pharma USA, Inc. has initiated a voluntary recall of two (2) lots (refer table below) of Quinapril and Hydrochlorothiazide Tablets USP 20mg / 12.5mg, to the consumer level from the US market due to presence of Nitrosamine Drug Substance Related Impurity (NDSRI), … See More
N-Nitroso-Quinapril above the proposed interim limit. Aurobindo Pharma USA, Inc. began shipping of the subject batches, QE2021005-A and QE2021010-A to customers nationwide May 2021.

-Affected product:
NDC No.: 65862-162-90, Product Name, strength, and pack: Quinapril and Hydrochlorothiazide Tablets USP, 20mg / 12.5mg, 90’s HDPE bottle, Lot number: QE2021005-A; QE2021010-A, Expiry: 01/2023

Risk Statement: Nitrosamines are common in water and foods, including cured and grilled meats, dairy products and vegetables. Everyone is exposed to some level of nitrosamines. These impurities may increase the risk of cancer if people are exposed to them above acceptable levels over long periods of time. To date, Aurobindo Pharma USA, Inc. has not received any reports of adverse events related to this recall.

Quinapril and Hydrochlorothiazide Tablets, USP are fixed-combination tablet that combines an angiotensin-converting enzyme (ACE) inhibitor, quinapril hydrochloride, and a thiazide diuretic, hydrochlorothiazide. This product is indicated for the treatment of hypertension, to lower blood pressure. Patients should contact their doctor or health care provider about whether to continue taking their medication, or whether to consider an alternative treatment prior to returning their medication.

Quinapril and Hydrochlorothiazide Tablets USP 20 mg / 12.5 mg are “Pink colored, scored, round shaped, biconvex, film-coated tablets, debossed with ‘D’ on scored side and ‘19’on other side”, supplied in 90’s HDPE bottle.

Qualanex, on behalf of Aurobindo Pharma USA, Inc., will be notifying its distributors and customers by phone and in writing to immediately discontinue distribution of the specific lots being recalled and to notify their sub-accounts. Aurobindo Pharma USA, Inc. is arranging for return of all recalled products to Qualanex. Instructions for returning recalled products are given in the recall letter.

Consumers should also contact their physician or healthcare provider if they have experienced any problems that may be related to taking or using this drug product.

This recall is being conducted with the knowledge of the U.S. Food and Drug Administration.

In case you experienced harm from this product, it is important to report it. It can help to detect & resolve issues and prevent others from being harmed, and it enables better surveillance.

Company name: Aurobindo Pharma USA, Inc.
Brand name: Aurobindo Pharma USA, Inc.
Product recalled: Quinapril and Hydrochlorothiazide Tablets USP, 20mg / 12.5mg, 90’s HDPE bottle
Reason of the recall: Due to presence of Nitrosamine Drug Substance Related Impurity (NDSRI), N-Nitroso-Quinapril
FDA Recall date: October 25, 2022

Source: www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/aurobindo-pharma-usa-inc-initiates-voluntary-nationwide-recall-two-2-lots-quinapril-and
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#blood #drugs #us #sub #vegetable #meat #ro-tel

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Walmart announced at 7:19 a.m. Wednesday via Facebook that the store was closed due to unidentified electrical issues. At 5:50 p.m. the company announced the store had reopened, but several departments were still closed, including dairy, frozen, meat, deli, bakery and online grocery pickup — which were … See More
emptied of stock due to spoilage concerns. By 10 a.m. Thursday, the company reported the store was back open and products were being trucked in and restocked.

Outage link: outagemap.ny.nationalgridus.com/
Source: www.oleantimesherald.com/news/walmart-reopens-restocks-after-power-outage/article_98cf1431-59d2-507f-b35b-b3d078e79ee8.html
Published: 2022-10-21
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#nationalgrid #walmart #poweroutage #1869plazadrive #olean #newyork #us #meat

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