Pfizer Vaccine, Lafayette, CO, USA

3 years ago •reported by user-mnjzj412

Pfizer Vaccine, Lafayette, CO, USA

Lafayette, Colorado, United States

I have had previous allergic reactions to nuts, but am happy to report I did not experience an allergic reaction as a result of having the Pfizer vaccine. I had it at about 4-5PM, and no immediate side effects. By the late evening my arm hurt and I didn’t want to lift it. By the next morning, the pain had decreased, and by that evening it was completely gone. I have never had Covid before :^) | Symptoms: Soreness

#featuredcovid19vaccinereports #pfizer #vaccine #covid19vaccine #pfizercovid19vaccine #lafayette #colorado #us

Pfizer Vaccine photo #1
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Related Reports

Propofol Injection Emulsion, USP - recalled due to the presence of particulates, USA

1 year ago •source www.fda.gov

Recall notice

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: www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/hospira-issues-voluntary-nationwide-recall-one-lot-propofol-injectable-emulsion-containing-benzyl
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Propofol Injection Emulsion, USP - recalled due to the presence of particulates photo #1
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Pfizer Propofol Injection Emulsion, USP - recalled due to Potential presence of visible particulate, USA

1 year ago •source www.fda.gov

Recall notice

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: www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/hospira-issues-voluntary-nationwide-recall-one-lot-propofol-injectable-emulsion-usp-containing
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Pfizer Propofol Injection Emulsion, USP - recalled due to Potential presence of visible particulate photo #1
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Pfizer Accureticâ„¢, quinapril and hydrochlorothiazide; and quinapril HCl/hydrochlorothiazide tablets - recalled due to N-NitrosoQuinapril, USA

2 years ago •source www.fda.gov

Recall notice

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.

- Accureticâ„¢ (quinapril HCl/hydrochlorothiazide) tablets, 10/12.5 mg
- Accureticâ„¢ (quinapril HCl/hydrochlorothiazide) tablets, 20/12.5 mg
- Accureticâ„¢ (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: Accureticâ„¢ (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: www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/pfizer-voluntary-nationwide-recall-lots-accuretictm-quinapril-hclhydrochlorothiazide-quinapril-and
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Pfizer Accureticâ„¢, quinapril and hydrochlorothiazide; and quinapril HCl/hydrochlorothiazide tablets - recalled due to N-NitrosoQuinapril photo #1
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Power Outage, Springhill Road, Lafayette, Calif, USA

1 month ago

A power outage was reported in the East Bay after a massive tree fell on top of cars in Lafayette overnight. It happened in the Springhill area on Springhill Road. The toppled tree also brought down some powerlines and caused power outages Tuesday morning, Mar 12. According … See More
to PG&E, power has been restored to the area.

Outage link: pgealerts.alerts.pge.com/outage-tools/outage-map/#current
Source: abc7news.com/fallen-tree-cars-damaged-lafayette-powerlines-down/14516970/
Published: 2024-03-12
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Power Outage, Southcity Pkwy, Lafayette, LA, USA

1 month ago

According to LUS’s outage map, 1,951 customers were experiencing outages as of 9:26 a.m. today Sunday, Mar 10 in the area of Southcity Pkwy off of Johnston Street. Power has been restored to the area.

Outage link: www.lus.org/map/
Source: www.klfy.com/local/lafayette-parish/lus-experiencing-power-outage-in-south-lafayette/
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Boil Water Advisory, Old Hopkinsville Rd, LaFayette, KY, USA

1 month ago

A boil water order has been issued for all customers in the city of Lafayette including customers with addresses 124-1500 Roaring Springs Rd and all addresses on North Main and South Main in Lafayette, Oakland Ave, Bryan Ave, Weathers Ave, Old Hopkinsville Rd, Church St, Harrison St, … See More
Cross St, Old Clarksville Pike, White St, Cheatam Ln, Canton Rd, Lane St, and Creek St.

Source: www.wkdzradio.com/2024/02/24/lafayette-area-under-boil-water-advisory/news-edge/
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Power Outage, Deer Hill Road, Lafayette, CA, USA

1 month ago

There were reports of a power outage in Contra Costa County. According to PG&E’s outage map, about 730 customers are affected by a power outage near Deer Hill Road in Lafayette on Monday afternoon, Feb 19. The outage started at 11.59 a.m. PST. The estimated time for … See More
restoration is 3:45 p.m. PST. PG&E is investigating the cause of the outage. Crews are working to restore power to the area.

Outage link: pgealerts.alerts.pge.com/outage-tools/outage-map/
Source: www.pge.com/en.html
Published: 2024-02-19
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Air mattress I didn’t receive, Texas, USA

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I received an item that was not an air bed mattress that I purchased and received a necklace instead and would like to report. Just like others, I saw when I googled this address because I did not recognize the item which was a silver necklace type … See More
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ADM Animal Nutrition Chicken, Swine, Cattle, & Horse Feed - recalled due to elevated levels of minerals, USA

2 weeks ago •source www.fda.gov

Recall notice

ADM Animal Nutrition announced that specific lots may contain elevated levels of calcium, phosphorus, magnesium, sodium and/or chloride and may harm chickens, swine, beef cattle and equine. ADM (NYSE: ADM), is recalling the following products: Pen Pals® Chicken Starter-Grower 25-lb bag (Product No 70009ACF46); Pen Pals Chicken … See More
Starter-Grower 50-lb bag (Product No. 70009AAA44); Pen Pals Chicken Starter-Grower 25-lb case (Product No. 70009AAABE); MoorMan’s ShowTec Sale Burst w/DF DEN 50-lb. bag (Product No 21256CVWE4); MoorMan's Show-Tec Burst Starter with DFCTC/DEN 50-lb. bag (Product No: 24320AYWE4); ShowTec BB 18 BMD 50-lb. bag (Product No. 18241AGNE4); ShowTec 14.5/6 BMD 50-lb. bag (Product No. 14560AGN); AMPT-A CTC/IGR 50-lb. bag (Product No. 54229XNK); ShowTec Hi Fat 18 BMD 50-lb. bag (Product No. 18007AGN); Seniorglo 50-lb. bag (Product No. 10130AB) and MotivAte 12-15 DEN 50-lb. bag (Product No. 12286CVW). One customer reported chicken deaths related to consumption of the Pen Pals Chicken Starter-Grower 25-lb bags.

The lot number for the Pen Pals Chicken Starter-Grower 25-lb bags involved in this recall is Lot 507650QN. This product may contain elevated levels of calcium and phosphorus, which could lead to leg deformities, trouble standing and walking, and can be fatal to chickens. This product was distributed between Feb. 29, 2024 and March 8, 2024, and could have been purchased through distributors in Iowa and Missouri.

The lot number for the Pen Pals Chicken Starter-Grower 50-lb bags and Pen Pals® Chicken Starter-Grower 25-lb case involved in this recall is Lot 506942QN. These products may contain elevated levels of magnesium, which can cause bone deformities, slow growth rate, watery feces and can be fatal to chickens. These products were distributed between Feb. 28, 2024 and March 14, 2024, and could have been purchased through distributors in Missouri, Ohio, South Carolina, Iowa, California and Oregon.

The lot number for the MoorMan’s ShowTec Sale Burst w/DF DEN 50-lb. bags involved in this recall is Lot 506664QN. This product may contain increased levels of sodium and chloride, which can lead to reduced feed intake, thirst and diarrhea. This product was distributed between Feb. 16, 2024, and March 1, 2024, and could have been purchased through distributors in Iowa, Wisconsin and Colorado.

The lot number for the MoorMan’s ShowTec Burst Starter w/DF CTC/DEN 50-lb. bags involved in this recall is Lot 506640QN. This product may also contain increased levels of sodium and chloride. This product was distributed between Feb. 16, 2024, and March 1, 2024, and could have been purchased through distributors in Iowa, Wisconsin and Colorado.

The lot number for the ShowTec BB 18 BMD 50-lb. bags involved in this recall is Lot 506939QN. This product may also contain increased levels of sodium and chloride. This product was distributed between Feb. 16, 2024, and March 1, 2024, and could have been purchased through distributors in California, Illinois, Arizona, Missouri, and Iowa. The lot number for the ShowTec 14.5/6 BMD 50-lb. bags involved in this recall is Lot 507900QN. This product may contain increased levels of calcium, which could cause reduced feed intake and feed conversion. This product was distributed between March 8, 2024, and March 18, 2024, and could have been purchased through distributors in Iowa.

The lot number for the AMPT-A CTC/IGR 50-lb. bags involved in this recall is Lot 507828QN. This product may contain increased levels of sodium, which could cause loose stools and central nervous system issues. This product was distributed on March 1, 2024, and could have been purchased through distributors in Missouri.

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The company initiated the recall once it was confirmed that these specific lots could contain harmful levels of calcium, phosphorus, magnesium sodium, and/or chloride. ADM has been in direct contact with the customers and distributors involved in this recall, and all product has been removed from retail shelves.

The lot number can be found at the bottom of the label. Customers who have purchased the recalled feed should immediately stop using it and return it to their distributor or directly to ADM Animal Nutrition for a full refund.

Company name: ADM Animal Nutrition
Brand name: Multiple Brand Names
Product recalled: Chicken Feed, Swine Feed, Cattle Feed, Horse Feed
Reason of the recall: Specific lots may contain elevated levels of calcium, phosphorus, magnesium, sodium and/or chloride and may harm chickens, swine, beef cattle and equine.
FDA Recall date: April 01, 2024

Source: www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/adm-animal-nutrition-recalls-select-pen-palsr-chicken-feed-moormans-showtec-swine-feed-ampt-cattle
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ADM Animal Nutrition Chicken, Swine, Cattle, & Horse Feed - recalled due to elevated levels of minerals photo #1
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Tech 1us Scam, MN, USA

1 week ago •reported by user-zwzhz382

I ordered a pair of what supposed to be a rechargeable all type weather camping lighter/ torch and received a cheap Chinese torch and a ear cleaner kit . No phone number or anything to contact them at all with the false product

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user-rgdc3993

Just like me!! I expected, as promised, a rechargeable plasma lighter. I received a Butane lighter that is totally empty and no recharging cables. That was my first clue.Totally scammed from what I expected. Going to ask for a total refund. If not received in two days, I will call my bank to cancel the charge as this is fraud.

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user-wwkcn515

Exactly the same. 3 expensive butane lighters which were supposed to be rechargeable. Fleeced. Fraud.

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Same thing, Dallas, TX, USA

5 days ago •reported by user-vcjnp739

I placed a order on March 12th from the same company and got a tracking number stayed watching it as it supposedly went to each destination till it stated delivered on March 27th. But nothing came, my husband stayed my the front door all day waiting for … See More
it, for nothing to arrive. I've reached out to customer service with no success to do anything. And im out of $150 of my hard working money just gone...... I'm so upset don't know who to turn to. The website stated they were affiliated with Amazon and it was a secured site so I believed it was ok...... how can they use a logo of such magnitude and not be real???
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