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Independence Lake County Park, Jennings Road, Whitmore Lake, Webster Township, MI, USA
Independence Lake beach has been closed due to high levels of E. Coli
1 month ago
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... 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
Lake Byllesby beach in Cannon Falls, MN closed due to E. coli, Lake Byllesby Beach, Echo Point Rd, Cannon Falls, MN 55009, USA
3 weeks ago
Lake Byllesby beach has been closed until further notice by Dakota County due to high E. coli levels. Beach water testing will resume on Tuesday, Sept. 6 when the lab reopens. Dakota County will notify the public when E.coli levels are safe for beach visitors.
My house is right on the road, Nicki's Place in Edgewater Park., Van Rossum Avenue, Edgewater Park, NJ, USA
3 weeks ago
Bus gives door to door service that uses the small alley right by my house that sits right ON the road. Van Rossum Avenue, Edgewater Park, and Nicki's Place. Your bus picks up a child at 7AM NJ, USA at his door not a bus stop of... any kind. There is a parallel road, West Franklin, that road which is a main road and we could sleep later if the bus took that road as there is ample room to turn around. The door to door pick up should not be our problem. The alley he comes doen is really just a small little road meant for access by the 8 houses on this street. My house was built in 1875 and sits literally right on the alley. I'm requesting the driver use West Franklin to pick up and drop off.
1 week ago
I turned my sink on and the water coming out has been brown for 2 days. When I checked my friends who alos lives on 6th the color is brown also. I don't think it is safe to drink.
1 year ago
1. Exposure to COVID positive staff and residents, due to failure to follow infection control protocol, over 20 staff infected. 2. COVID positive test results withheld 10 days from staff and continuing to make them work, stating they are past their 10 days post test date, but... notified staff of results 10 days after lab notification. 3. Forcing staff to work COVID positive residents with just a surgical mask. 4. We are just now after a few weeks of having COVID in building, fitting for respirator masks, most staff failing test. 5. Over 60% of building COVID positive not including staff. 6. Careless mistake of moving a few residents who were COVID negative to the COVID positive lockdown and then residents contracted COVID and fell ill, coverups by management. 7. Working 1 nurse and 1 CNA on COVID positive lockdown units with 20-30 COVID positive symptomatic ill residents. 8. Threatening staff they will be fired if they do not do as told, while staff is being exposed everyday. 9. Management will not step foot in COVID lockdown, trying to force LPNs to start IVs, does not want us to send ill residents out to hospital but we have no proper tools to care for their symptoms of distress. 10. Management breaking isolation protocol by pulling workers off COVID positive units to work COVID negative, exposing staff and residents. 11. Two nurses on night shift in building, forced to work 2 COVID lockdown halls with 1 nurse and 0-1 aide. 12. We are terrified but obligated to work or loose our job and harassed that bad reference given to next job.
Source: Osha.gov | Receipt Date: 2020-12-03
1 year ago
1. The employer is not letting staff know that other staff members and residents are testing positive for COVID-19. 2. They only have 4 housekeepers for the whole building so it is not getting cleaned properly. 3. The CDC reported that there were 3 positive cases at... the facility, but according to the administrator, that was a lie and there have not been any positive cases. 4. There was a resident that was confirmed positive yesterday, and last week an employee also tested positive. I have yet to hear from anyone in management about this matter
Source: Osha.gov | Receipt Date: 2020-04-30
2 students test positive for Covid-19, Whitmore Lake Elementary School, Barker Road, Whitmore Lake, MI, USA
1 year ago
2 students at Whitmore Lake Elementary School located on Barker Road in Whitmore Lake recently tested positive for Covid-19.
2 students test positive for Covid-19, Whitmore Lake High School, Whitmore Lake Road, Whitmore Lake, MI, USA
1 year ago
2 students at Whitmore Lake High School located on Whitmore Lake Road in Whitmore Lake recently tested positive for Covid-19.
The boil order has been lifted in Niles Township. The boil order was in effect for one week and two days. The tests came back negative and state has lifted the order.
Recent Interesting Reports
4 days ago
I ordered an outdoor dog kennel. I tried to contact company for shipping info and no response. I filed a scam to credit card company. Then I recieved a small package with some type of phone charger in it.. far from a dog kennel
Proper Trade LLC/My Stellar Lifestyle is voluntarily recalling Wonder Pill lot 20210912 and lot 31853-501, expiry 09/24, packaged in 10-count blisters co-packaged in a carton and in 60-count bottles to the consumer level. Proper Trade LLC/My Stellar Lifestyle 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 presence of tadalafil in Wonder Pill capsules 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 the Wonder Pill with undeclared tadalafil may experience serious 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. To date, Proper Trade LLC/ My Stellar Lifestyle has not received any reports of adverse events related to this recall.
The product is marketed as a dietary supplement for male sexual enhancement and is packaged in 10-count blisters co-packaged in a carton, ASIN B0B6CWC9NK, and packaged in a 60-count bottle. The affected lots include lot numbers’ 20210912 & 31853-501, Expiry 09/24. The product can be identified by the labels below. The product was distributed via the internet and fulfilled by Amazon at www.amazon.com and Walmart at www.walmart.com, nationwide in the USA.
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.
Proper Trade LLC/ My Stellar Lifestyle is notifying its customers by this press announcement and sending Amazon & Walmart messages to its customers and is arranging for return of all recalled products. Consumers that have Wonder Pill capsules which is being recalled should stop using the product.
Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to taking or using this drug product. Adverse reactions or quality problems experienced with the use of this product may be reported to the FDA's MedWatch Adverse Event Reporting program either online, by regular mail or by fax.
This recall is being conducted with the knowledge of the U.S. Food and Drug Administration.
Company name: Proper Trade LLC/My Stellar Lifestyle
Brand name: My Stellar Lifestyle
Product recalled: Wonder Pill Capsules
Reason of the recall: Product contains undeclared tadalafil
FDA Recall date: September 28, 2022
My Yorkie is in the hospital fighting for her life after eating Dream bones. She's bleeding from the rectum severely., Huntsville, Alabama, USA
1 week ago
She began to have diarrhea 3 days ago after eating the first Dream bone. We didn't relate the problem. She got a second one the next day and the diarrhea continued for 3 days. Last night blood began to pour from her. Today they are trying to see where the bleeding is coming from to save her. | Symptoms: Diarrhea, Bloody Stool
I got this covid booster, and flu shot at the same time. Zero side effects so far, and I am on day 3 now. I assume by now I am in the clear. The picture says moderna, but he assured me it was the pfizer.
bought product from Stuncloth, freshlook colorblend Gray contacts. Instead sending me what I ordered and PAID for I received MAXIY BROWN CONTACTS. This what I ordered AND IT WAS ALSO CONFIRMED IN THE EMAIL I RECEIVED BELOW. Items in this shipment Freshlook Colorblends Colored Contacts Lenses Non... Prescription (Buy 3 get 1 Free) × 2 Gray. I WANT MY MONEY BACK, OR THE PRODUCT THAT ORDERED AND PAID FOR!!!!
1 week ago
Family Dollar is initiating a voluntary retail level product recall of certain products regulated by the U.S. Food and Drug Administration (FDA) that were stored and inadvertently shipped to certain stores on or around May 1, 2022 through June 10, 2022 due to product being stored outside... of labeled temperature requirements. This notice covers the recall of Over-the-Counter Medical Devices. An earlier notice issued July 21, 2022 covered a related recall of Over-the-Counter Pharmaceutical Products. To date, Family Dollar has not received any consumer complaints or reports of illness related to this recall. This recall is being conducted out of an abundance of caution.
- Recalled products:
900260 900260 CLEARBLUE SMART COUNTDOWN PRGNCY TST 1CT
900794 900794 LS SKYN NON LATEX LUBRICATED CONDOM 3CT
901260 901260 VERIQUICK PREGNANCY TEST 1CT
902343 902343 FIRST RESPONSE 2 CT
903409 903409 SKYN ORIGINAL NON LATEX CONDOM 12CT
903415 903415 SKYN ELITE NON LATEX CONDOM 12CT
939504 939504 VERIQUICK PREGNANCY TEST 1 CT
900752 900752 AT HOME MARIJUANA TEST STRIP
902816 902816 TROJAN ULTRA RIBBED LUBED 3CT
903756 903756 VERIQUICK PREGNANCY TEST 2 CT
999763 999763 TROJAN ULTRA THIN CONDOM LATEX 3CT
998221 998221 SKYN ELITE LARGE NON LATEX CONDOM 12CT
998869 998869 PREFERRED UTI TEST 1 CT
900265 900265 LIFESTYLES ULTRA SENSITIVE CONDOMS 12CT
900531 900531 CLEAR EYES CONTCT LENS DRPS LBRCTNG .5FO
999009 999009 B L BIOTRU MULTI PURPOSE SOLUTION 4 FLOZ
902274 902274 GS SALINE SOLUTION 12FL OZ
901443 901443 KY JELLY LUBRICANT 2 FL OZ
901960 901960 OPTI FREE REPLENISH MULTI PURPOSE 2 OZ
999801 999801 SIMPLY SALINE NASAL MIST 3.1 OZ
900457 OPTI FREE PURE MST DSINFCTNG SLTN 4FL OZ
902139 902139 DENTEMP ONE STEP .077OZ
906018 906018 FIXODENT ORG CREAM 2.4OZ
998762 998762 DRTALBOT TDDLR TTHPSTE BRSH TUTTI FRUTTI
905076 905076 CURAD STRNG WATRPRF STRIP 1IN 20CT
906312 906312 GS DENTURE CLEANSER GRN TAB 40CT
999619 999619 FIXODENT ADH CREAM ULTRA MAX HOLD 2.2OZ
999037 999037 CURAD FIRST AID KIT
903377 903377 POLIGRIP POWER MAX HOLD 2.2OZ
999417 999417 NEW SKIN LIQUID BANDAGE CLEAR .3FL OZ
900737 900737 TRVL KIT TOTHBRSH CAP PASTE IN POUCH 1CT
901239 901239 FIXODENT ORG CREAM TRAVEL .75OZ
906131 906131 POLIDENT DENTURE CLNS TAB 28CT
900334 900334 POLIGRIP ADH CREAM FREE 2.4OZ
906023 906023 GS DENTURE CLEAN OVRNT TAB 40CT
901634 901634 POLIDENT DENTURE CLEANSERS 84 CT
901777 901777 POLIDENT OVERNIGHT WHITENING TAB 28CT
906402 906402 FIXODENT ADH CREAM WITH SCOPE 2OZ
999632 999632 POLIGRIP EXTRACARE ADHESIVE CREAM 2.2OZ
900085 900085 SUPER POLIGRIP ADH CREAM .75OZ
900723 900723 POLIGRIP DENTURE ADHESIVE ORIGINAL 2.4OZ
This recall goes to the retail store level. Not all of the products listed were sent to all stores. Family Dollar has notified its affected stores asking them to check their stock immediately and to quarantine and discontinue the sale of any affected product. Customers that may have bought affected product may return such product to the Family Dollar store where they were purchased without receipt.
This recall does not apply to Connecticut, Maine, Massachusetts, New Hampshire, Rhode Island, Vermont, Washington, Alaska, or Hawaii as Family Dollar does not have any stores in Alaska or Hawaii and no Family Dollar stores in any of the other states received any products subject to this recall. Customers should contact their physician or health care provider if they have experienced any problems that may be related to using these products.
Company name: Family Dollar
Brand name: Multiple brand names
Product recalled: Various OTC medical products
Reason of the recall: Product was stored outside of labeled temperature requirements.
FDA Recall date: September 16, 2022
14 hours ago
I received this package and nothing is in it the tracking number is 9400136206335672417717 I paid for this item I want what I paid for
Antica Farmacista Ocean Citron Hand Sanitizer - recalled due to product contains benzene, Seattle, WA, USA
1 week ago
Salon Technologies International. Inc. is voluntarily recalling one lot of Antica Ocean Citron Hand Sanitizer (alcohol) Gel 65%, Lot 1166A. Expiration 6/18/2023 to the consumer level. Firm lab testing has found the product to contain benzene. Benzene is classified as a human carcinogen. Exposure to benzene can... occur by inhalation, orally, and through the skin. Depending on duration and level of exposure, it can result in cancers including leukemia and blood cancer of the bone marrow and blood disorders which can be life-threatening.
Salon Tech International, Inc. has not received any reports of adverse events related to this recall. The product is used to help reduce bacteria, that potentially can cause disease, when soap and water are not available. 512 bottles of Antica Ocean Citron Hand Sanitizer (alcohol) Gel 65%, Lot 1166A, Expiration 6/18/2023 was distributed in the Seattle, Washington area.
Salon Technologies International. Inc. has notified its distributors by email and is arranging for return of all recalled products. Consumers that have product which is being recalled should stop using and return unused product to where it was obtained.
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: Salon Technologies International Inc.
Brand name: Antica Farmacista
Product recalled: Ocean Citron Hand Sanitizer
Reason of the recall: Product contains benzene
FDA Recall date: September 19, 2022
2 days ago
I received an order I had placed and paid for the product as well as postage that had a fraudulent postage label and was I required to pay an additional $4.80 to accept the package.
Last 30 days