Lowes Foods of Robinhood Road, 3372 Robinhood Rd, Winston-Salem, NC 27106, USA

An employee(1) at UPS CUSTOMER CTR in SANTA FE, NM tested positive for Covid-19 and the company is on the Rapid Response COVID-19 Watchlist Event Date: 08/09/2022,

Source: env.nm.gov See Less

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Multiple employees(2) at UPS CUSTOMER CTR in LAS CRUCES, NM tested positive for Covid-19 and the company is on the Rapid Response COVID-19 Watchlist Event Date: 08/09/2022,

Source: env.nm.gov See Less

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Multiple employees(2) at VILLAGE OF MILAN in MILAN, NM tested positive for Covid-19 and the company is on the Rapid Response COVID-19 Watchlist Event Date: 08/09/2022,

Source: env.nm.gov See Less

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Multiple employees(2) at VUPOINT RESEARCH in LAS CRUCES, NM tested positive for Covid-19 and the company is on the Rapid Response COVID-19 Watchlist Event Date: 08/09/2022,

Source: env.nm.gov See Less

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Multiple employees(3) at WALMART NEIGHBORHOOD MARKET in LAS CRUCES, NM tested positive for Covid-19 and the company is on the Rapid Response COVID-19 Watchlist Event Date: 08/09/2022,

Source: env.nm.gov See Less

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Multiple employees(2) at WALMART SUPERCENTER in ALBUQUERQUE, NM tested positive for Covid-19 and the company is on the Rapid Response COVID-19 Watchlist Event Date: 08/09/2022,

Source: env.nm.gov See Less

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Multiple employees(2) at WELLS FARGO BANK in GALLUP, NM tested positive for Covid-19 and the company is on the Rapid Response COVID-19 Watchlist Event Date: 08/09/2022,

Source: env.nm.gov See Less

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Multiple employees(2) at WELLS FARGO BANK in ALBUQUERQUE, NM tested positive for Covid-19 and the company is on the Rapid Response COVID-19 Watchlist Event Date: 08/09/2022,

Source: env.nm.gov See Less

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Multiple employees(2) at WHOLE FOODS MARKET in ALBUQUERQUE, NM tested positive for Covid-19 and the company is on the Rapid Response COVID-19 Watchlist Event Date: 08/09/2022,

Source: env.nm.gov See Less

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Multiple employees(2) at WHOLE FOODS MARKET in SANTA FE, NM tested positive for Covid-19 and the company is on the Rapid Response COVID-19 Watchlist Event Date: 08/09/2022,

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The Washtenaw County Health Department and the Washtenaw County Parks and Recreation Commission announced that Independence Lake beach has been closed for swimming the due to high levels of E. coli bacteria. The beach will reopen once follow-up tests confirm levels are low enough to safely swim... See More again.

According to the news this is the third time officials have closed Independence Lake beach this summer due to high levels of E. coli bacteria

Source: clickondetroit.com See Less

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Random package from 188 S Mountain House Parkway. Never ordered this. Nothing else inside but this random bracelet? Odd. See Less

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Your delivery driver ran me off the road as engaging into the left lane.
Using a company my son life at risk because your is not courteous to share the road.
Should kept straight through and caused you guys millions in lawsuit damages.
License plate of the... See More truck: BCZ R76
Need this gentleman written up or fired! See Less

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Encore is recalling Beef Selection in Gravy multipack dog food because the Beef Steak with Potatoes in Gravy tin, within the multipack, may contain small pieces of metal. This product was distributed nationwide in the United Kingdom.

Encore Beef Selection in Gravy (Multipack) (5 tins x 156g)... See More Batch code: LU1-343
Best before: 09 December 2024

Encore Beef Selection in Gravy (Multipack) (5 tins x 156g)
Batch code: LU1-302
Best before: 29 October 2024

Encore Beef Steak with Potatoes in Gravy (Individual tin) (156g)
Batch code: LU1343D
Best before: December 2024

Pet-owners: We urge customers who have bought this product not to feed it to their dog and return it to the store with or without a receipt from where it was bought for a full refund.

In case your pet experienced harm from extraneous materials, 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: Encore
Product recalled: Encore Beef Selection in Gravy (Multipack), Encore Beef Selection in Gravy (Multipack), Encore Beef Steak with Potatoes in Gravy (Individual tin)
FSA Recall date: 07/18/2022

Source: food.gov.uk See Less

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Item was arrived 07-30 -22 Teterboro. I didn’t receive my order from Jlo Beauty tracking number should is in Teterboro since 7-30-22. Tracking number is 9261290278840003. See Less

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Hospira, Inc., a Pfizer company, is voluntarily recalling one lot of Propofol Injectable Emulsion, USP (containing benzyl alcohol), 100 mL Single Patient Use Glass Fliptop Vial; lot DX9067, to the user level due to a visible particulate observed in a single vial during annual examination of retain... See More samples. The product lot was distributed nationwide to wholesalers/ hospitals/Department of Defense in the United States from June 10, 2020 through June 26, 2020.

The recalled product is:
- Propofol Injectable Emulsion, USP 100 mL Single Patient Use Glass Fliptop Vial, NDC: Vial: 0409-4699-54 Carton: 0409-4699-24, Lot Number: DX9067, Expiration Date Presentation: 01 MAY 2023, Configuration/Count: 1 g/100 mL, Single Patient Use Glass Fliptop Vial Case of 10 Units.

Risk Statement: Patients receiving the impacted product are at risk of experiencing life-threatening adverse clinical effects including but not limited to: blockage of blood vessels, including decreased blood flow to the brain, heart attack, pulmonary embolus, and tissue necrosis. Hypersensitivity reactions and transmission of infectious disease can also occur.

To date, Hospira, Inc. has not received reports of any adverse events associated with this issue for this lot. Propofol is an intravenous general anesthetic and sedation drug for use in the induction and maintenance of anesthesia or sedation. Propofol Injectable Emulsion, USP is a terminally sterilized (TS) product. It is a sterile, nonpyrogenic emulsion containing 10 mg/mL of propofol suitable for intravenous administration supplied in a single patient use fliptop vial.

Wholesalers or hospitals with an existing inventory of the lot, which is being recalled, should stop use and distribution and quarantine immediately. If you have further distributed the recalled product, to the wholesale or hospital level/institution, please notify any accounts or additional locations which may have received the recalled product from you. Hospitals/Institutions should inform Healthcare Professionals in your organization of this recall.

Company name: Hospira Inc, A Pfizer Company
Brand name: Hospira
Product recalled: Propofol Injection Emulsion, USP
Reason of the recall: Potential presence of visible particulate
FDA Recall date: July 13, 2022

Source: fda.gov See Less

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Ultra Supplement LLC is voluntarily recalling lot number DAP272109, exp 4/1/26 of Sustango capsules packaged in 10-count blisters packaged in a carton to the consumer level. Ultra Supplement was notified by Amazon that laboratory analysis has found the product to be tainted with tadalafil, an ingredient in... See More FDA approved products for treatment of male erectile dysfunction in the family of drugs known as phosphodiesterase (PDE-5) inhibitors. The product was distributed via the internet and fulfilled by Amazon at www.amazon.com nationwide in the USA. To date, Ultra Supplement has not received any reports of adverse events related to this recall.

On December 17, 2020, FDA issued a press release that warned consumers to avoid certain products found on Amazon, eBay and other retailers due to hidden and potentially dangerous drug ingredients. It also encouraged online marketplaces to ensure these products are not sold on their platforms.

The presence of tadalafil in Sustango makes this product an unapproved drug for which the safety and efficacy has not been established and therefore, subject to recall.

Consumers with underlying medical issues who take Sustango capsules with undeclared tadalafil may experience health risks. For example, PDE-5 inhibitors may interact with nitrates found in some prescription drugs (such as nitroglycerin) lowering blood pressure to dangerous levels that may be life-threatening. Consumers with diabetes, high blood pressure, or heart disease often take nitrates. The product is marketed as a dietary supplement for male enhancement and is packaged in 10-count blisters packaged in a carton, ASIN X0024468I9. The affected cartons include Lot DAP272109, Exp. 4/1/26. The product can be identified by the label below.

Ultra Supplement is notifying its distributors and customers by this press announcement and by Amazon Messaging and is arranging for return of all recalled products. Consumers that have Sustango capsules Lot# DAP272109 should stop using the product.

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: Ultra Supplement LLC
Brand name: Sustango
Product recalled: Dietary Supplement for Male Enhancement
Reason of the recall: Undeclared Tadalafil
FDA Recall date: July 25, 2022

Source: fda.gov See Less

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That Bay Area Homeless Shelter Is A Horrible Place And They Letting My Partner Be Out On The Street Homeless To Purposely Separate Us While I'm 5 Months Pregnant Going Through A Lot Of Pain Here By Myself
My Partner Ran Out Of Gas On July 13th... See More And Couldn't Make It Back Here Before Curfew Time At 10pm I Was Worried And Didn't Know What He Was Going Through Until The Next Morning Because His Phone Isn't On He Had No Way To Contact Me Or The Shelter He Begged His Mom For A Few Bucks And Made It Back The Morning If July 14th And This Shelter Gave Him No Chance Told Him He Had To Leave That's No Way To Be Treating People We Both Have Tried Numerous Of Times To See If They Would Let Him Back And They Literally Are Keeping Us Separated On Purpose It Seems Because Neither Of Us Have Done Anything Wrong For Him To Be Out On The Streets Like This While I'm Here Alone 5 Months Pregnant See Less

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The CFIA announced the recall of raw frozen Primal Patties for Dogs Beef Formula because it may be contaminated with Listeria monocytogenes, posing a risk of cross-contamination and illness after handling the pet food. This product was sold in British Columbia. As of August 2, 2022, the... See More company has not received any reports of incidents or illness in Canada.

The recalled product is:
- Primal Patties – Beef Formula, 6 lb, Case UPC: 854495006173, Unit UPC: 850334004164, Lot code number: W10068709, Best by date: 05/22/23.

The lot code number and best by date can be found on the back of the product packaging above the Primal Pet Foods Inc. red oval logo. Only lot code number W10068709 is included is this recall.

Animals that become infected with Listeria monocytogenes could display symptoms similar to humans. Listeria monocytogenes can affect animals eating the product, and there is risk to humans from handling the products, especially if they have not thoroughly washed their hands after having contact with the products or any surfaces exposed to the products.

Consumers should immediately stop using the recalled product and dispose of the product.

In case you are experiencing Listeria monocytogenes symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain, and diarrhea, it is important to report it. It can help to detect & resolve outbreaks early and prevent others from being harmed, and it enables better surveillance. If symptoms persist, seek medical care. If symptoms persist, seek medical care.

Source: recalls-rappels.canada.ca See Less

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This is completely unsafe. How the hell would they get my address with my son's girlfriend's name on it? This is absolutely ridiculous and I'm willing to take this to court See Less

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