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Pancheros

Updated: February 3, 2021 12:00 PM

Covid-19 OSHA Complaint, Pancheros Mexican Grill, 1035 Lawrence Drive, BURLINGTON, IA, 52601, USA

Pancheros Mexican Grill, 1035 Lawrence Drive, BURLINGTON, IA, 52601, USA

February 3, 2021 12:00 PM

“Health: 1. Employees are not wearing mask correctly, and are not changing gloves often enough.


Source: Osha.gov | Receipt Date: 2021-01-04 See Less
Reported By SafelyHQ.com User

Covid-19 OSHA Complaint, Pancheros Mexican Grill, 2261 4th St SW, Mason City, Iowa 50401, USA

Pancheros Mexican Grill, 2261 4th St SW, Mason City, Iowa 50401, USA

November 3, 2020 12:00 PM

“September 15, 2020

Health:

1. Employees are exposed to the COVID-19 pandemic. Employees with symptoms are not being isolated and work along side their coworkers. Employees are not practicing social distancing of 6 feet and typically work within 3 feet of each other. Employees are not wearing... See More face coverings as of about 09/11/2020.

Location: 2261 4th St SW, Mason City, Iowa

Alleged Hazards: 1, Employees Exposed: 4
Source: Osha.gov | Receipt Date: 2020-09-15
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Reported By SafelyHQ.com User

Covid-19 OSHA Complaint, Pancheros Mexican Grill, 650 Community Drive, North Liberty, Iowa 52317, USA

Pancheros Mexican Grill, 650 Community Drive, North Liberty, Iowa 52317, USA

September 7, 2020 12:00 PM

“August 13, 2020

Health:

1. Employees are exposed to the COVID-19 pandemic. The employer is not following the Centers for Disease Control and Prevention's COVID-19 guidance for workplaces. Employees work about one foot apart from each other. Face coverings do not stay on employees' faces and slide... See More down. Employees wear face coverings below the nose and not over the nose. Employees wear face coverings under the chin without coverage to the mouth and nose. There is no partition shield between employees and customers. Customers are not required to wear face coverings.

Location: counter area, grill area

Alleged Hazards: 1, Employees Exposed: 2
Source: Osha.gov | Receipt Date: 2020-08-13
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Reported By SafelyHQ.com User

Recent Interesting Reports

1 era dosis Pfizer, Parque Bicentenario, Av. Río Amazonas, Quito, Ecuador

Symptoms: Soreness
Parque Bicentenario, Av. Río Amazonas, Quito, Ecuador

July 28, 2021 9:18 PM

“Despite the large number of people there were, everything was pretty fast and organized. I just had a little pain in my arm, where I got the vaccine for a day. See Less
Reported By SafelyHQ.com User

July 23, 2021 12:03 AM

“Company name: HIS
Brand name: HIS
Product recalled: Dietary Supplement for Weight Loss
Reason of the recall: Undeclared Sibutramine
FDA Recall date: July 22, 2021
Recall details: Palisades Park, NJ, HIS is voluntarily recalling all lots and all presentations of Miss Slim (10 count & 30 count... See More capsules) to the consumer level. HIS decided to recall Miss Slim after it was contacted by the FDA regarding the presence of sibutramine in the product.

Sibutramine was an FDA-approved drug used as an appetite suppressant for weight loss but was withdrawn from the market because of safety issues. The presence of sibutramine in Miss Slim renders it an unapproved drug for which safety and efficacy has not been established and therefore subject to a recall. To date, HIS has not received any reports of adverse events related to this recall.

The product is marketed as a dietary supplement and is packaged 10 count UPC (742137605030) and 30 count UPC (609728434472) capsules. The product sold online at missslimusa.com.

Risk Statement: Products containing sibutramine pose a threat to consumers because sibutramine is known to substantially increase blood pressure and/or pulse rate in some patients and may present a significant risk for patients with a history of coronary artery disease, congestive heart failure, arrhythmias or stroke.

HIS is notifying its customers by website missslimusa.com and is arranging for return of all recalled products. Consumers that have Miss Slim which is being recalled should stop using it. 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.

Check the full recall details on fda.gov

Source: FDA
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July 11, 2021 3:25 PM

“I saw the chain saw advertised on Facebook and ordered it 4 months ago and still have not recieved it they got my money though. And can not get a real tracking number. See Less
Reported By SafelyHQ.com User

July 13, 2021 4:17 PM

“I ordered the Battery-Powered Wood Cutter, this is the second one I’ve ordered and have not received I either want my money back for 2 or I want them sent. On April 15th they shipped a Battery Powered WOOD CUTERR, I have not received it yet, plus... See More I ordered one before this, I would like to know where they are,  Aphitrite Technology limited See Less
Reported By SafelyHQ.com User

July 19, 2021 6:51 PM

“Ordered hand chainsaw from them off Facebook. I got a weird metal string thing that I almost threw away because I nor anyone I asked knew what the hell it was. What a ripoff!!! I am trying to get my money back, but if they think for... See More one moment that I'm going to pay to have that piece of sh*t sent back to them, they better think again!! See Less
Reported By SafelyHQ.com User

July 19, 2021 9:02 PM

“Company name: Alpha Male Plus
Brand name: Alpha Male Plus
Product recalled: Alpha Male Plus Male Enhancer fruit chew
Reason of the recall: Undeclared Tadalafil
FDA Recall date: July 19, 2021
Recall details: Tucson, AZ, Alpha Male Plus is voluntarily recalling all lots within expiry of Alpha... See More Male Plus Male Enhancer fruit chews to the consumer level. FDA analysis has found the product to be tainted with tadalafil, an ingredient known as a phosphodiesterase (PDE-5) inhibitor found in a FDA approved product for the treatment of male erectile dysfunction. The presence of tadalafil in Alpha Male Plus Male Enhancer renders the product an unapproved drug for which safety and efficacy have not been established and, therefore, subject to recall.

Risk Statement: Consumers with underlying medical conditions who take Alpha Male Plus Male Enhancer 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, Alpha Male Plus has not received any reports of adverse events related to this recall.

The tainted Alpha Male Plus Male Enhancer product was manufactured by Dr Manuel Mascarenas M.D. in Tucson, Arizona located at 5190 E Farness Dr Ste 104, 85712. Dr Mascarenas is the originator and manufacturer of these products for the global market. Alpha Male Plus was selected to act as the US distributor and distribute these products for the US market.

The tadalafil ingredient was never disclosed or made known to its US distributor and was only discovered through FDA laboratory analysis. Dr Manuel Mascarenas is solely responsible for the creation, formulation and proliferation of this product. Through the use of concealment, dishonest means and an unknowing 3rd party Dr Mascarenas was able to begin distributing this mislabeled and potentially harmful product to the US market.

Alpha Male Plus was marketed as a dietary supplement for male sexual enhancement and is packaged in 1strip per foil pouch within a cardboard box, UPC [8 60003 03770 6] [8 60003 74512 0].

The affected Alpha Male Plus Male Enhancer includes all lots. The product was distributed nationwide in the USA via internet directly to consumers via their website.

Company is notifying its distributors and customers by e-mail and is arranging for return of all recalled products. Consumers/distributors/retailers that have product which is being recalled should stop using or return to place of purchase/discard/contact their doctor, etc.

This recall is being conducted with the knowledge of the U.S. Food and Drug Administration.

Check the full recall details on fda.gov

Source: FDA
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July 7, 2021 11:46 AM

“Yesterday I bought and gave my dog two dream one twist dog treats. A couple hours later he was acting sick. Head down, not himself. He's a very energetic blue Lacy so this is unlike him. Yesterday evening I noticed he was trying to poo but couldn't.... See More He refused his normal treats (not the dream bone but he gets blue buffalo bits after potty breaks) this was another red flag . My boy never turns down a treat.
All last night he was restless. It's now 10 am on the day after giving him the dream bone twists. He's still restless, can't get comfy, lays down then stands up then sits down with his head down. Won't eat, even things he normally loves. I've rubbed his belly and tried to comfort him. I let him out and walked him around a bit to try and help his bowels move along. Still nothing. He ate a bit of grass which is normal when dogs don't feel good. A bit later he started puking a massive amount and I could see alot of undigested dream bone in it. Those dream bones are the only new thing hes had and now he's really sick. I'm scared after reading about other law suites and issues regarding this product that my dog might have obstructed bowels from eating eat. I'm watching him closely and ready to take him to the vet as soon as I see if he's going to improve after puking or not. Vet visits are really expensive and if he needs surgery or declines further I'm going to raise hell. It's not okay for money hungry corporates to line their pockets while falsely advertising its products as safe knowing dam well it's killing beloved animals. My dog deserved a treat not a fight for his life.
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Reported By SafelyHQ.com User

July 14, 2021 7:27 PM

“I have had this bait and switch happened to me twice, once by this company and once by another company. The little wires are used by campers to cut small branches. Both times. I paid through PayPal. I ordered the rechargeable battery mini saw pruner. I received... See More a wire. Contacted the seller and the seller offered me a 50% refund, I told the seller I wanted 100% of my money back. The seller then replied that he would request a 60% refund but he could not give back 100% unless I returned the product to China. It costs like 30 dollars to send to China from the US even though they claim they are US based. The seller said they had shipped product and paid logistic cost to ship it to me and would I please accept the 60% and he hoped I understood. These bait and switch practices are illegal in the US. I escalated the case to Paypal. Then waited for the review. I then received an email from PayPal stating the seller had provided a shipping number and they found in favor of the seller. This message is generated by an auto responder. I then called PayPal and requested to speak to a PayPal agent. With in 2 minutes the person could see the Seller had done this over and over. They refunded my money and apologized for the inconvenience the Seller had caused me. It takes some time and effort, but persistence pays off. Also, it I s not your responsibility to return the product they shipped back to them at your expense.

They are located in Tennesee the key is to start the case through Paypal, when Paypal finds in favor of the seller. Call PayPal and speak with an agent. The message you received is sent out by an auto responder. PayPal agents can see that it us a recurring issue and your money will be refund. If you paid by credit card contact thr company snd ask them to do a charge back.
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Reported By SafelyHQ.com User

July 13, 2021 8:00 PM

“Company name: Innoveix Pharmaceuticals, Inc.
Brand name: Innoveix Pharmaceuticals, Inc.
Product recalled: Injectable Semorelin / Ipamorelin 3mg and injectable AOD-9604 3mg
Reason of the recall: Potential lack of sterility assurance
FDA Recall date: July 13, 2021
Recall details: Innoveix Pharmaceuticals, Inc. is voluntarily recalling the following lots... See More of sterile compounded drug products, within expiry. The products are being recalled due to a lack of assurance of sterility. These concerns arose following a routine inspection of the pharmacy by FDA.

Administration of a drug product intended to be sterile, that is not sterile, could result in serious infections which may be life-threatening. To date, Innoveix Pharmaceuticals, Inc. has not received any reports of adverse events related to this recall. This voluntary recall is being conducted out of an abundance of caution and to promote patient safety, which is the pharmacy's highest priority.

The affected products are injectable Semorelin / Ipamorelin 3mg and injectable AOD-9604 3mg. The products can be used for various indications as prescribed. The products can be identified by an Innoveix Pharmaceuticals, Inc. label. The products were distributed in glass vials contained in a small 3 inch by 3 inch white box.

Products were distributed nationwide to both customers and/or medical facilities. A full list of the affected products with the applicable lot numbers and expiration dates is as follows:

Product Lot/Expiry
Semorelin / Ipamorelin 3mg Lot# SIP210; Exp: 12/15/2021
Lot# SIP215; Exp: 01/14/2022
Lot# SIP220; Exp: 01/23/2022

AOD-9604 3mg Lot# AOD205; Exp: 11/09/2021
Lot# AOD210; Exp: 11/18/2021
Lot# AOD 215; Exp: 12/15/2021
Lot# AOD202; Exp: 11/09/2021

Check the full recall details on fda.gov

Source: FDA
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July 11, 2021 10:50 AM

“Yeah I never received this item I would like my money back, Ordered off of Facebook got from yeahyard a miniature saw pruner
Thank you See Less
Reported By SafelyHQ.com User