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Mercy Convenient Care - Zero Street, Fort Smith, AR, USA

Latest report: March 19, 2021 6:03 PM
DT

I am reporting first shot of Pfizer vaccine

3 years ago

I have not had Covid before but have had 3 Covid tests. This was the first shot of two of the Pfizer vaccine. I took a Tylenol about an hour before the shot as it was recommended to me to do. I received the shot yesterday (3/18)... See More and I did "feel" the shot. I had some tenderness at shot location on arm throughout the day. The clinic was very busy with a waiting line to check in that was not observing any social distancing. The process itself was very streamlined and went relatively fast. Each person was asked to sit down and wait for 15 minutes after their shot before leaving, but, I noticed many either did not or left well before 15 minutes. My arm remained somewhat tender at the site of the shot through the day yesterday, but I do not notice it today. Othewise, no other symptoms. See Less
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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. See Less
544


Hospira, Inc., a Pfizer company, is voluntarily recalling one lot of Propofol Injectable Emulsion (containing benzyl alcohol), 100mL Single Patient Use Glass Fliptop Vial; lot EA7470, to the user level due to visible particulates observed in two vials during annual examination of retention samples. The product lot... See More was distributed nationwide to wholesalers/hospitals in the United States from July 16, 2020 through July 24, 2020. To date, Pfizer has not received reports of any adverse events associated with this issue for this lot.

Risk Statement: Patients receiving the impacted product have a remote probability of experiencing potential adverse events, such as 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.

Propofol is an intravenous general anesthetic and sedation drug for use in the induction and maintenance of anesthesia or sedation. Propofol Injectable Emulsion 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 Glass Fliptop Vial. The NDC, Lot Number, Expiration Date, and Configuration details for Propofol Injectable Emulsion are indicated below.

Product: Configuration/Count Propofol Injectable Emulsion, 100 mL Single Patient Use Glass Fliptop Vial
NDC: Vial: 0409-4699-54 Tray: 0409-4699-24
Lot Number: EA7470
Expiration Date: 01 JUNE 2023
Presentation: 1g/100 mL, Single Patient Use Glass Fliptop Vial
Configuration/Count: Tray of 10 Units

Pfizer places the utmost emphasis on patient safety and product quality at every step in the manufacturing and supply chain process. Pfizer has notified direct consignees by letter to arrange for return of any recalled product.

Wholesalers or hospitals with an existing inventory of the lot, which is being recalled, should discontinue use, stop distribution and quarantine immediately. If you have further distributed the recalled product, please notify your accounts and/or any additional locations which may have received the recalled product. 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: August 22, 2022

Source: fda.gov
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303


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
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303


Pfizer is voluntarily recalling Accuretic (quinapril HCl/hydrochlorothiazide) tablets distributed by Pfizer as well as two authorized generics distributed by Greenstone (quinapril and hydrochlorothiazide and quinapril HCl/ hydrochlorothiazide) to the patient (consumer/user) level due to the presence of a nitrosamine, N-nitroso-quinapril, above the Acceptable Daily Intake (ADI) level.... See More To date, Pfizer is not aware of reports of adverse events that have been assessed to be related to this recall. 

Pfizer will recall six lots of Accuretic tablets, one lot of quinapril and hydrochlorothiazide tablets and four lots of quinapril HCl/ hydrochlorothiazide tablets. 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.

These products are indicated for the treatment of hypertension.  Lowering blood pressure reduces the risk of fatal and nonfatal cardiovascular events, primarily strokes and myocardial infarctions. The products have a safety profile that has been established over 20 years of marketing authorization and through a robust clinical program. Pfizer believes the benefit/risk profile of the products remains positive based on currently available data. Although long term ingestion of N-nitroso-quinapril may be associated with a potential increased cancer risk in humans, there is no immediate risk to patients taking this medication. Patients currently taking the products should consult with their doctor about alternative treatment options.

The NDC, Lot Number, Expiration Date, and Configuration details for these products are indicated in the tables in the link below and photos of the products can be found below. The product lots were distributed nationwide to wholesalers and distributors in the United States and Puerto Rico from November 2019 to March 2022.

- Accuretic™ (quinapril HCl/hydrochlorothiazide) tablets, 10/12.5 mg
- Accuretic™ (quinapril HCl/hydrochlorothiazide) tablets, 20/12.5 mg
- Accuretic™ (quinapril HCl/hydrochlorothiazide) tablets, 20/25 mg
- quinapril and hydrochlorothiazide tablets, 20/25 mg
- quinapril HCl/hydrochlorothiazide tablets, 20/12.5 mg
- quinapril HCl/hydrochlorothiazide tablets, 20/25 mg

Pfizer has notified direct consignees by letter to arrange for return of any recalled product.

Wholesalers and distributors with an existing inventory of the lots, listed in the table above, should stop use and distribution and quarantine the product immediately.

If you have further distributed the recalled product, please notify any accounts or additional locations which may have received the recalled product from you.

Company name: Pfizer
Brand name: Accuretic, Greenstone Brand
Product recalled: Accuretic™ (quinapril HCl/hydrochlorothiazide); quinapril and hydrochlorothiazide; and quinapril HCl/hydrochlorothiazide tablets
Reason of the recall: Presence of a nitrosamine, N-nitroso-quinapril
FDA Recall date: March 22, 2022

Source: fda.gov
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303


I received a order fromJANE 371 LITTLE FALLS RD STE4….CEDAR GROVE NJ 07009, I never orderd any thing from this company, gray size M from CYKLAS
How did this company get my address?!!I don’t like this, I will return if possible, it made out of very cheap... See More material lie a Jersey materal plus it’s to small See Less
54


Storms are causing power outages and flooding in the River Valley and Northwest Arkansas. Sebastian County Emergency Manager said there are significant problems across the county. There are downed power lines in Barling. Almost 50% of Greenwood is without power and there are issues with some transformers... See More there. As of 6:45 a.m., there were more than 14,000 power outages in Sebastian County, more than 3,800 people without power in Benton County, and hundreds without power in Crawford, Washington, Scott and Franklin counties.

OG&E Energy Corp.:outagemap.oge.com
Southwestern Electric Power Co: outagemap.swepco.com.s3.amazonaws.com

Source: 4029tv.com
Published: 2023-07-14
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54


I received a blue table cloth but did not order one. I am confused as to how my name and address was used by this person correctly and afraid that I am being charged for it. See Less
54


More than 9,800 electric customers in Fort Smith remained without power Sunday morning after strong thunderstorms blew through the city late Saturday and early Sunday, according to reports. As straight line winds reported to be up to 100 mph ripped eastward, a tornado hit near Prairie View... See More east of Paris about 1:10 a.m. Sunday according to County's emergency management director. At 7:20 a.m. Sunday, there were 5,491 customers of Oklahoma Gas & Electric Co. without power in south Fort Smith and the Barling area. There were another 4,330 customers without power in north Fort Smith and 1,671 without power in Arkoma.

Outage link: outagemap.oge.com
Source: swtimes.com
Published: 2023-06-18
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My order nr. 202312264734****.
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Nutraceutical Corporation has issued a nationwide recall for its Heritage Store Hydrogen Peroxide Mouthwash due to a risk of poisoning. The recall, announced by the U.S. Consumer Product Safety Commission (CPSC) was initiated due to the mouthwash containing ethanol at a concentration level that requires child-resistant packaging... See More under the Poison Prevention Packaging Act (PPPA). The packaging of the recalled products is not child-resistant, posing a risk of poisoning if swallowed by young children. To date, no incidents or injuries related to this recall have been reported.

The recall affects both Wintermint and Eucalyptus Mint flavors of the Heritage Store Hydrogen Peroxide Mouthwash. The product is packaged in dark opaque brown bottles with a white lid, featuring a pink and white label displaying the Heritage Store logo, product name, and flavor. All lots of these two mouthwashes are included in the recall, totaling approximately 102,100 units.

If you or a loved one are harmed by this product, it is important to report it. Reporting can help to detect & resolve outbreaks early and prevent others from being harmed, and enables better surveillance. If symptoms persist, seek medical care.

Source: cpsc.gov
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I so it on Beat Buy website I thought it was legit but I canceled my order never received my refund
I was looking for a cheap sofa when I can across the web site and ordered the sofa and I am still trying to get my money back they want answer my emails See Less


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