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1835 North Main Street, Roswell, New Mexico, United States
Updated: August 3, 2022 12:00 PM
An employee(1) at WALGREENS in ROSWELL, NM tested positive for Covid-19 and the company is on the Rapid Response COVID-19 Watchlist Event Date: 08/03/2022,
Multiple employees(2) at WALGREENS in ROSWELL, NM tested positive for Covid-19 and the company is on the Rapid Response COVID-19 Watchlist Event Date: 07/27/2022,
Multiple employees(3) at WALGREENS in ROSWELL, NM tested positive for Covid-19 and the company is on the Rapid Response COVID-19 Watchlist Event Date: 07/06/2022,
Multiple employees(2) at WALGREENS in ROSWELL, NM tested positive for Covid-19 and the company is on the Rapid Response COVID-19 Watchlist Event Date: 06/28/2022,
Multiple employees(2) at WALGREENS in ROSWELL, NM tested positive for Covid-19 and the company is on the Rapid Response COVID-19 Watchlist Event Date: 02/02/2022,
Multiple employees(3) at WALGREENS in ROSWELL, NM tested positive for Covid-19 and the company is on the Rapid Response COVID-19 Watchlist Event Date: 01/26/2022,
An employee(1) at WALGREENS in ROSWELL, NM tested positive for Covid-19. Event Date: 10/06/2020, RR-2885
Recent Interesting Reports
2 weeks ago
Vi-Jon, LLC is revising a previously reported list of all flavors of Magnesium Citrate Saline Laxative Oral Solution within expiry that were voluntarily recalled to the consumer level to include product that was distributed in the United States, Canada and Panama. This includes all lots of Cherry... Flavor and Grape Flavor of Magnesium Citrate Saline Laxative Oral Solution, 10 FL OZ (296 mL) within expiry. To date, Vi-Jon, LLC is aware of 3 (three) reports of serious adverse reactions potentially related to this recall. Vi-Jon, LLC is in the process of investigating these reports.
On July 14, 2022, Vi-Jon, LLC recalled all lots of Magnesium Citrate Saline Laxative Oral Solution Lemon Flavor, 10 FL OZ (296 mL) within expiry. The recall was initiated after Vi-Jon, LLCs third party microbial testing identified the presence of Gluconacetobacter liquefaciens.
Risk Statement: Immunocompromised patients, who consume this product, may be at increased risk for invasive infections caused by Gluconacetobacter liquefaciens that could lead to serious, life-threatening adverse health consequences. The product is used for relief of occasional constipation (irregularity) and generally produces bowel movement in ½ to 6 hours. The product is packaged in a 10 oz clear round plastic bottle. In addition to the lemon flavor, the recall includes the Cherry flavor and Grape flavor.
On August 3, 2022, the Recall product list has been updated to include the products noted below.
CANADA Equate Canada 300 mL Lemon Magnesium Citrate
NPN # NPN 80015316
UPC # 079068004923
CANADA Life 300 mL Lemon Magnesium Citrat
NPN # NPN 80015316
UPC # 057800856412
CANADA Life 300 mL Cherry Magnesium Citrate
NPN # NPN 80015316
UPC # 057800856405
CANADA Personnelle 300 mL Lemon Citrate
NPN # NPN 80015316
UPC # 055989029306
PANAMA CRUZ BLANC 10OZ LEMON MAG CIT
NPN # N/A
UPC # 308697403082
The product was distributed in the United States, Canada and Panama to wholesale and retail outlets. Vi-Jon, LLC is continuing their investigation into the cause of the problem.
Vi-Jon, LLC is notifying its customers by phone and email and is arranging for return or destruction of all recalled product. Consumers that have this recalled product should stop using and return any remaining product to the place of purchase.
This recall is being conducted with the knowledge of the U.S. Food and Drug Administration.
In case you experienced 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.
Company name: Vi-Jon, LLC
Brand name: Multiple brand names
Product recalled: Magnesium Citrate Saline Laxative Oral Solution
Reason of the recall: Microbial contamination with Gluconacetobacter liquefaciens
FDA Recall date: August 04, 2022
Driver illegally parks in a NO STOPPING ANYTIME spot on the Embarcadero in San Francisco during RISH HOUR TRAFFIC blocking the turning lane wasting everyone’s time because he couldn’t legally park 100
No one should be so inconsiderate that they illegally park during horrible rush hour traffic... when there is LEGAL parking 100 feet away. The driver refused to move his truck saying he had to park there. WTF? Blocked the turning lane for not just a couple of minutes but for at least 30. Rude Rude Rude. It’s hard enough having to driving home on a busy Friday afternoon but one of your drivers illegally parking his Amazon Delivery truck right in front of a NO STOPPING ANYTIME sign deserves to be reprimanded. You know it’s BS and all the people he held up know it too. license # 45675K3
I received a 10cent plastic fan in a mailer. So I am assuming they are going to use the tracking number to show I did receive a pkg. But a 10 cent plastic fan is not a piece of furniture to store craft items.
1 week ago
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... 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.
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
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... 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
DISTRIBUTOR RFR, LLC. is voluntarily recalling lot #48656, Exp. 01/2025 of SANGTER Energy Supplement, 3000 mg, packaged in 7-count blister packs within a carton to the consumer level. FDA analysis has found the product to contain undeclared sildenafil. Sildenafil is a phosphodiesterase (PDE-5) inhibitor found in FDA-approved... products for the treatment of male erectile dysfunction. The presence of sildenafil in SANGTER makes it an unapproved new drug for which the safety and efficacy has not been established and, therefore subject to recall. To date, DISTRIBUTOR RFR, LLC. has not received any reports of adverse events related to this recall.
The tainted product is marketed as a dietary supplement for male sexual enhancement and is packaged in a 7-count blister pack within a carton, UPC 0 705632 523285, and was distributed through retail stores in the state of Florida from 02/01/2002 to 07/20/2022 and Nationwide in the USA through our website from 02/01/2002 to 07/20/2022 www.sangter.com.
Distributor RFR, LLC is notifying its distributors and customers through this notice and is arranging for the return of all recalled products. All customers are urged to stop consuming the product marked with this lot, and to contact their physician or health care provider if they have experienced any problems that may be related to taking or using this medication.
Risk Statement: Use of SANGTER with undeclared sildenafil may pose a threat to consumers because it may interact with nitrates found in some prescription drugs (such as nitroglycerin) and may cause a significant drop in blood pressure that may be life threatening. People with diabetes, high blood pressure, high cholesterol, or heart disease often take nitrates. Among the adult male population who are most likely to use these products, adult males who use nitrates for cardiac conditions are at the most at risk from these products.
Company name: Distributor RFR, LLC
Brand name: SANGTER
Product recalled: SANGTER Energy Supplement, 3000mg
Reason of the recall: Undeclared Sildenafil
FDA Recall date: August 02, 2022
I didn’t receive my order tracking 9261290278840003, USPS Teterboro Distribution Center, Industrial Avenue, Teterboro, NJ, USA
2 weeks ago
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.
I am a resident of 817 Rose Lane and over a period of nearly 4 weeks I’ve reported a dead branch on a tree on the parkway hanging over my driveway and street. It nearly scrapes the top of my car and my lawncare people have to... duck the branch to cut my grass. This is dangerous and I have had no active response from public works. Spoke to someone from public works and city hall with no results 3 times.
Last 30 days