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IHOP
Updated: April 1, 2021 12:00 PM
Covid-19 OSHA Complaint, IHOP, 2071 E Beltline, GRAND RAPIDS, MI, 49525, USA
IHOP, 2071 E Beltline, GRAND RAPIDS, MI, 49525, USA
April 1, 2021 12:00 PM
“1. The establishment has flies and spiders and it's always very dirty and not cleaned properly; the sinks have mold in them. 2. The general manager has tested positive for COVID after having symptoms and still coming in. The other manager's son got it and management is telling employees that because... See Morethey have not been in direct contact they don't have to be tested. This even though employees have worked with the manager. 3. The establishment was never closed and was still open serving customers the very next day. 4. Employees who thought they had COVID were still required to come into work until their test came back positive even though they were sick and showing symptoms.
Source: Osha.gov | Receipt Date: 2020-09-22 See Less”
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Covid-19 OSHA Complaint, IHOP, 2071 E Beltline, GRAND RAPIDS, MI, 49525, USA
IHOP, 2071 E Beltline, GRAND RAPIDS, MI, 49525, USA
April 1, 2021 12:00 PM
“1. All employees have not been instructed on Covid protocol. 2. Covid-19 disinfectant is not utilized and proper sanitation procedures are not followed when cleaning tables. High touch points do not get cleaned at all and bathrooms have no log-in display for public. 3. Employees are required to come... See Morein, even if throwing-up or displaying Covid symptoms. 4. Employees are not screened prior to their shift.
Alleged Hazards: 1, Employees Exposed: 1
Source: Osha.gov | Receipt Date: 2020-09-21 See Less”
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3 individuals tested positive for Covid-19, IHOP, 2025 Main St, Alamosa, CO 81101, USA
IHOP, 2025 Main St, Alamosa, CO 81101, USA
March 4, 2021 12:00 PM
“3 individuals at IHOP- Alamosa in Alamosa county tested positive for Covid-19. The outbreak began on 3/1/21
Source: colorado.gov See Less”
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Covid-19 OSHA Complaint, IHOP, 38045 47th Street East, Palmdale, CA 93552, USA
IHOP, 38045 47th Street East, Palmdale, CA 93552, USA
November 10, 2020 12:00 PM
“Per Call: As employee tested positive for COVID-19 and management has not notified EE's nor cleaned facility. 7/14/2020 the EE had tested positive management has been aware. EE's have told the manager but has not done anything to clean or notify affected EE's.
Alleged Hazards: 2,
Source: Osha.... See Moregov | Receipt Date: 2020-07-16 See Less”
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Covid-19 OSHA Complaint, IHOP, 10150 N McCarran Blvd, Reno, NV 89503, United States
IHOP, 10150 N McCarran Blvd, Reno, NV 89503, United States
October 13, 2020 12:00 PM
“1. One employee was admitted to the hospital with COVID-19, and the employer did not inform the other employees that could have been in contact with the employee.
Alleged Hazards: 1,
Source: Osha.gov | Receipt Date: 2020-09-03 See Less”
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Covid-19 OSHA Complaint, IHOP, 4764 Valley View Boulevard Northwest, Roanoke, Virginia, USA
IHOP, 4764 Valley View Boulevard Northwest, Roanoke, Virginia, USA
October 13, 2020 12:00 PM
“1. Social distancing recommendations not adhered to in the lobby and other areas.
2. Employees traveling to hot spots (i.e. Myrtle Beach) and returning without quarantine.
3. No hot water for employees to wash their hands with.
Source: Osha.gov | Receipt Date: 2020-07-16 See Less”
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Covid-19 OSHA Complaint, IHOP, 235 New State Highway, Raynham, Massachusetts 02767, USA
IHOP, 235 New State Highway, Raynham, Massachusetts 02767, USA
September 28, 2020 12:00 PM
“Excessively warm temperatures are causing employees to experience respiratory distress. The air conditioning system is not working properly.
The restaurant is not following precautions against Covid-19 infection, including not taking employees temperatures.
Alleged Hazards: 2, Employees Expo... See Moresed: 20
Source: Osha.gov | Receipt Date: 2020-09-10 See Less”
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IHOP, 4210 N Cicero Ave., Chicago, IL, USA, IHOP, 4210 N Cicero Ave, Chicago, IL, USA
IHOP, 4210 N Cicero Ave, Chicago, IL, USA
September 23, 2020 9:00 AM
“Report date: Sep 21, 2020
10. Adequate handwashing sinks properly supplied and accessible
- comments: instructed to provide handwashing signage at handsink in main prep area and handsink in men's washroom.
51. Plumbing installed; proper backflow devices
- comments: backflow preventer devi... See Morece not located behind ice machine. Instructed to install so that it can be located to be serviced and maintained.
51. Plumbing installed; proper backflow devices
- comments: instructed to repair (hot) faucet handle at handsink in main prep area (water continously dripping).
51. Plumbing installed; proper backflow devices
- comments: noted water leaking from pipe behind dishmachine. Instructed to repair.
54. Garbage & refuse properly disposed; facilities maintained
- comments: instructed to clean and maintain rear outside garbage area. Noted some litter and unnecessary articles stored. Must remove.
55. Physical facilities installed, maintained & clean
- comments: instructed to clean, maintain and reorganize rear storage area and in 2nd floor storage area to rpevent pest harborage.
55. Physical facilities installed, maintained & clean
- comments: instructed to regrout floor tiles with deep seam under and around ice machine and floors under and around hot water tank in rear storage area.
55. Physical facilities installed, maintained & clean
- comments: instructed to clean and maintain floors and wall behind and under dishmachine. Noted water pooling. Instructed to keep floors dry to prevent pest harborage.
55. Physical facilities installed, maintained & clean
- comments: instructed to detail clean and maintain floors under and around front coffee station area
55. Physical facilities installed, maintained & clean
- comments: instructed to clean and remove unnecessary articles stored in rear storage area and in 2nd floor storage including inside employee locker room.
64. Public health nuisance
- comments: observed employees (cook and server) not wearing face coverings properly. Not covering their nose while preparing and serving customers. Instructed management that all employees are required to cover their nose and mouth with a face covering while working inside the restaurant. Citation issued (corrected on site) see comments
Source: chicago.gov See Less”
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An employee test positive for Covid-19, IHOP, 2304 N Main St, Roswell, NM, USA
IHOP, 2304 N Main St, Roswell, NM, USA
September 21, 2020 12:00 PM
“An employee(1) at IHOP RESTAURANT in ROSWELL, NM tested positive for Covid-19. Event Date: 09/20/2020, RR-1272
Source: env.nm.gov See Less”
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Covid-19 OSHA Complaint, IHOP, 9115 E 56th St, Indianapolis, Indiana 46216, USA
IHOP, 9115 E 56th St, Indianapolis, Indiana 46216, USA
September 17, 2020 12:00 PM
“Employees not wearing masks.
Source: Osha.gov | Receipt Date: 2020-08-13 See Less”
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Recent Interesting Reports
March 25, 2021 9:01 AM
“Company name: Sanit Technologies LLC d/b/a Durisan
Brand name: Durisan
Product recalled: Antimicrobial Hand Sanitizer
Reason of the recall: Due to microbial contamination
FDA Recall date: March 24, 2021
Recall details: Sanit Technologies LLC d/b/a Durisan announces a voluntary recall of the lot... See Mores listed in the table below of Durisan Antimicrobial Hand Sanitizer, Non-Alcohol products in various sizes listed. The products are being recalled due to microbial contamination. Specifically, out of specification results for bacterial count for Burkholderia cepacia complex and Ralstonia pickettii. The issue was discovered during a routine audit focused on production scale-up during the height of the pandemic.
Check the link below for the full list of Durisan Antimicrobial Solutions Hand Sanitizer Sizes and Lot Numbers. To date, no reports of adverse reactions or customer complaints have been reported related to this recall.
The product was packaged in sizes ranging from 18mL credit cards, to bottles sized in 118, 236, 300 and 550 mL and 1000mL wall mounted dispenser refills. Pictures are available in the attached related file.
Use of a hand sanitizer contaminated with Burkholderia cepacia complex and Ralstonia pickettii, can range from no reaction to serious infections in a person with a hand wound or scrapes because the bacteria could enter the bloodstream, especially in patients with compromised immune systems. Health care professionals who use this contaminated hand sanitizer and tend to an at-risk patient, such as one with cystic fibrosis, could lead to adverse events ranging from a localized infection to lung or bloodstream infections, which could require patient hospitalization.
The product is intended to be applied topically to help reduce bacteria on the skin that could cause diseases when soap and water are not available. The product can be identified by examples of the product labels below. The product was manufactured from Feb. 1, 2020 until June 30, 2020, and distributed to selected retailers nationwide in the United States.
Durisan has provided written notification to its distributors and retailers and is alerting customers via this voluntary recall. Consumers that have the product which is being recalled are advised to destroy it immediately.
Consumers with questions regarding this recall can contact Durisan at 941-351-9114 [Call: 941-351-9114] , 8:30 am - 4:30 pm Eastern time, Monday through Friday or by e-mail at customerservice@durisan.com. Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to using this drug product.
Check the full recall details on fda.gov
Source: FDA See Less”
Helpful
1 person found this review helpful
March 31, 2021 12:02 PM
“Company name: Nuri Trading LLC
Brand name: Thumbs Up 7, Shogun-X, 69MODE
Product recalled: Dietary Supplement for male sexual enhancement
Reason of the recall: Undeclared Sildenafil, Tadalafil, Vardenafil
FDA Recall date: March 31, 2021
Recall details: Nuri Trading is voluntarily recalling all... See Morelots within expiry of Shogun-X 7000, Thumbs Up 7 (Black) 25K, Thumbs Up 7 (White) 11K, and 69MODE Blue 69 capsules to the consumer level. FDA analyses have found these products to contain undeclared tadalafil, sildenafil, and/or vardenafil. Sildenafil,tadalafil, and vardenafil are ingredients known as phosphodiesterase (PDE-5) inhibitors found in FDA approved products for the treatment of male erectile dysfunction.
The presence of sildenafil, tadalafil, and/ or vardenafil in Shogun-X 7000, Thumbs Up 7 (Black) 25K, Thumbs Up 7 (White) 11K, and 69MODE Blue 69 capsules make them unapproved new drugs for which the safety and efficacy have not been established and, therefore subject to recall.
Consumers with underlying medical issues who take Shogun-X 7000, Thumbs Up 7 (Black) 25K, Thumbs Up 7 (White) 11K, 69MODE Blue 69 capsules with undeclared sildenafil,tadalafil, and/or vardenafil 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, Nuri Trading has not received any reports of adverse events related to this recall. These tainted products are marketed as dietary supplements for male sexual enhancement and are packaged in blister foil sheets in a box. Each box contains 10 capsules. These products were distributed via internet and fulfilled by amazon at www.amazon.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.
Nuri Trading LLC is notifying its customers by this press announcement and via email of this recall. Consumers that have Shogun-X 7000, Thumbs Up 7 (Black) 25K, Thumbs Up 7 (White) 11K, 69MODE Blue 69, which are being recalled should stop using and destroy them. Consumers with questions regarding this recall can contact Nuri Trading by phone at (201) 380-1046 Monday to Friday from 9AM to 5PM eastern time or e-mail nuritrading17@gmail.com. For more information, please visit www.nuritradingusa.com.
Consumers should contact their physicians or healthcare provider if they have experienced any problems that may be related to takin 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.
Check the full recall details on fda.gov
Source: FDA See Less”
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After first Moderna shot, Sebastopol, CA, USA
Symptoms: Other
Body Ache
Soreness
Sebastopol, CA, USA
March 26, 2021 5:51 PM
“Sore arm first night, much like a flu shot. In subsequent days had achy lymph nodes in armpit, neck and upper chest. No big deal, just rather odd. 9 days after shot I woke with first Atrial fib in almost 6 weeks (had second Cardiac ablation last summer that we hoped would "fix" it). I had Afib episo... See Moredes next two nights, decreasing in intensity, but certainly requiring meds and monitoring. Since been diagnosed with Afib bit over 2 years ago had never had it multiple days in a row before.
Since then, every days it's less problematic. Now just an hour of feeling a tad funky in the afternoons.Asked my cardiologist if he'd had other patients with similar reactions and he said "yes", but mostly after second vaccination. Seems as if the inflammation that's triggered by vaccine as body responds and creates antibodies to virus, triggers "twitchy" susceptible heart into freaking out (my language, not his!) Makes me rather dread how I"m going to feel next week after second shot, But will certainly not deter me to get fully covered. See Less”
Helpful
1 person found this review helpful
March 31, 2021 10:00 AM
“Company name: Ummzy LLC
Brand name: Thumbs Up 7, Shogun, Krazy Night
Product recalled: Dietary Supplement for male sexual enhancement
Reason of the recall: Undeclared Sildenafil, Tadalafil, Vardenafil
FDA Recall date: March 31, 2021
Recall details: Palisades Park, NJ, Ummzy LLC is voluntarily r... See Moreecalling all lots of Thumbs up 7 Red 70K, Shogun-X 15000mg, and Krazy Night capsules to consumer level. FDA analysis has found the product to contain undeclared tadalafil sildenafil & Vardenafil. Tadalafil, Sildenafil & Vardenafil are ingredients known as phosphodiesterase (PD-5) inhibitors found in FDA approved products for the treatment of male erectile dysfunction. The presence of Tadalafil Sldenafil & Vardenafilin Thumbs up 7 Red 70K, Shogun-X 15000mg, and Krazy Night capsules makes them unapproved new drugs for which the safety and efficacy have not been established and, therefore subject to recall.
Consumers with underlying medical issues who take Thumbs up 7 Red 70K, Shogun-X 15000mg, and Krazy Night capsules with undeclared Tadalafil Sildenafil & Vardenafil 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, Ummzy LLChas not received any reports of adverse events related to this recall. This tainted product is marketed as a dietary supplement for male sexual enhancement and is packaged in blister foil sheets in a box containing 10 capsules. The affected lot numbers of Thumbs up 7 Red 70K, Shogun-X 15000mg, and Krazy Night includes all lots. Thumbs up 7 Red 70K, Shogun-X 15000mg, and Krazy Night was distributed nationwide in the USA via internet and fulfilled by amazon at www.amazon.com.
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. Ummzy LLC is notifying its customers by this press announcement and via e-mail of this recall.
Consumers that have Thumbs up 7 Red 70K, Shogun-X 15000mg, and Krazy Night, which is being recalled should stop using and destroy them. Consumers with questions regarding this recall can contact Ummzy LLC by phone at 201-416-9325 Monday to Friday from 9AM to 5PM or e-mail ysknabe75@gmail.com. For more information, please visit www.ummzyllc.com.
Consumers should contact their physicians 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.
Check the full recall details on fda.gov
Source: FDA See Less”
Helpful
April 6, 2021 9:13 PM
“Got my first shot yesterday afternoon at Walgreens. Felt fine most of the evening. Woke up at 1am and my left arm (I had the shot in my left arm) was numb along with the left side of my face. I started to panic thinking great it’s a stroke but I read about temporary Bell’s palsy and calmed down and... See Morewent to sleep. Woke up at 8:30. My arm was very sore which got worse as the day went on, I was very fatigued and had a low fever which Tylenol got rid of. Aches and pains came and went all day. My top lip on my left side of my mouth is still numb and parts of my face feels numb still but I look fine and feel fine otherwise. 30 hours later i would say the worst is the arm pain, I can’t really use my arm. I suggest getting it in your non dominant arm/hand which was suggested to me. Overall the numbness was scary but I think the vaccine is worth it. See Less”
Helpful
1 person found this review helpful
April 4, 2021 6:56 PM
“The CDC announced that they are currently investigating a multistate outbreak of Salmonella infections where 19 people have been reported sick from 8 states (CA, KY, MS, NH, OK, OR, TN, WA). Eight people of the total have required hospitalization but no deaths have been reported to date.
Accordin... See Moreg to the outbreak notice, there are reports of wild songbirds, such as pine siskins (small, streaked, yellow-tinged songbirds in the finch family) sick with the same strain of Salmonella that is making people sick in this outbreak. Salmonella germs can spread between species of birds, to pets, and to people.
You can get sick when you touch your mouth with unwashed hands after touching wild birds, bird feeders or bird baths, or your pets that have contact with wild birds.
CDC advises to:
- Clean and disinfect your bird feeder and bird bath weekly or when they are visibly dirty.
- Do not touch or hand-feed wild birds with your bare hands.
- Always wash your hands with soap and water
- Call your healthcare provider right away if you have any of these severe Salmonella symptoms
Most people infected with Salmonella develop diarrhea, fever, and stomach cramps 6 hours to 6 days after being exposed to the bacteria and the illness usually lasts 4 to 7 days, and many recover without treatment.
Check the CDC website for the full investigation details cdc.gov
Source: CDC See Less”
Doctor Visit: Yes
Diagnosis: Salmonella
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1 person found this review helpful
March 30, 2021 10:00 AM
“Company name: Bit & Bet LLC
Brand name: Thumbs Up 7
Product recalled: Blue 69K Dietary Supplement for male sexual enhancement
Reason of the recall: Undeclared Sildenafil and Tadalafil
FDA Recall date: March 30, 2021
Recall details: Bit & Bet LLC is voluntarily recalling all lots of Thumbs Up 7... See MoreBlue 69K capsules to consumer level. FDA analysis has found the product to contain undeclared sildenafil and tadalafil. Sildenafil and tadalafil are ingredients known as phosphodiesterase (PDE-5) inhibitors found in FDA approved products for the treatment of male erectile dysfunction.
The presence of sildenafil and tadalafil in Thumbs Up 7 Blue 69K capsules make them unapproved new drugs for which the safety and efficacy have not been established and, therefore subject to recall. Consumers with underlying medical issues who take Thumbs Up 7 Blue 69K capsules with undeclared sildenafil and 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, Bit & Bet has not received any reports of adverse events related to this recall. To date, Bit & Bet has not received any reports of adverse events related to this recall This tainted product is marketed as a dietary supplement for male sexual enhancement and is packaged in blister foil sheets in a box labeled with UPC 6 17135 89467 3. Each box contains 10 capsules. The affected lot numbers of Thumbs Up 7 Blue 69K includes all lots. Thumbs Up 7 Blue 69K was distributed via internet and fulfilled by amazon at www.amazon.com nationwide in the USA.
On December 17, 2020, FDA issued a press release that warned consumers to avoid certain products found on Amazon, e Bay 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. Bit & Bet LLC is notifying its customers by this press announcement and via email of this recall. Consumers that have Thumbs up 7 Blue 69K, which is being recalled should stop using and descard them.
Consumers with questions regarding this recall can contact Bit & Bet LLC by phone at (201) 208-2836 Monday to Friday from 9AM to 5PM or e-mail thumbsup7blue@gmail.com. For more information, please visit www.thumbsup7blue.com. Consumers should contact their physicians or healthcare provider if they have experienced any problems that may be related to takin 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.
Check the full recall details on fda.gov
Source: FDA See Less”
Helpful
March 29, 2021 10:43 PM
“First injection:
No issues with injection and no side effects.
Second injection:
Immediately following injection, blood ran down my arm. They claimed that a vein was punctured, but that the vaccination went in just fine. I questioned them again to make sure. And they insisted it was fine. The f... See Moreirst night following injection, my body was uncomfortable and I was unable to get into a deep sleep. 24hrs after injection, the injection site was surrounded by a large patch of red skin that was hot to the touch. At 28 hours, fatigue and malaise set in. At 48hrs, I felt markedly better, although still fatigued. The injection site was much less inflamed. See Less”
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2 people found this review helpful
March 17, 2021 11:00 AM
“Company name: PNHC, LLC d/b/a Heal the World
Brand name: Heal the World
Product recalled: Hand Sanitizer
Reason of the recall: Because they resemble water bottles; risk of ingestion
FDA Recall date: March 17, 2021
Recall details: Raleigh, North Carolina, PNHC, LLC, d/b/a Heal the World, is vol... See Moreuntarily recalling all lots of Heal the World hand sanitizer packaged in 9.6 fl. oz containers to the consumer level. The products are being recalled because they resemble 9.6ounce water bottles. The recall does not affect any other Hand Sanitizer products from PNHC, LLC and/or Heal the World.
- Heal the World Hand Sanitizer (9.6 FL. OZ (285 mL)). NDC: 73333-285-01. Lot Nos. SAA21, SAA24, SAA27, SAA22, SAA23, SAA29, SAA26, SAA28, SAA25, SAA32, SAA55, SAA56, SAA44, SAA60.
To date, PNHC, LLC, d/b/a Heal the World has received no reports of adverse reactions and no complaints have been received. Ingesting hand sanitizer, which is intended for topical use, could potentially result in alcohol toxicity. Symptoms of alcohol toxicity may range from lack of coordination, slowed or slurred speech, drowsiness to coma, which can be fatal. Furthermore, ingesting alcohol can affect the brain and cause impaired driving or operating heavy machinery. Alcohol can also interact with numerous drugs which may result in serious adverse effects. Ingesting alcohol by people with alcohol addiction may interfere with maintaining abstinence. Additionally, people with alcohol addiction may seek large amounts of ethanol-based hand sanitizers as a substitute.
The product is intended to be applied topically to help reduce bacteria on the skin that could cause diseases when soap and water are not available and is packaged in 9.6 ounce plastic bottles. The product can be identified by the bottle’s label pictured below. Product was distributed to selected retailers in the United States.
PNHC, LLC has provided notification to its distributors and retailers. Distributors and retailers that have product which is being recalled should stop distribution. While the product is not available for purchase and has not been available for several months, if a consumer has product which is being recalled he or she is advised to contact the entity who sold the product to consumer for return.
Consumers with questions regarding this recall can contact PNHC, LLC at 813-434-0741 from 9:00 am- 5:00 pm EST, Monday through Friday. Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to using this product.
Check the full recall details on fda.gov
Source: FDA See Less”
Helpful
March 29, 2021 9:50 PM
“My wife and I wanted to get the CoV2 vaccine but had significant concerns about the messenger RNA versions.
Anyway, we got the J&J vaccine, and we are satisfied with it.
However, some things need to be stated. My wife had a 103.3-degree fever the night of her shot. I didn't feel great, but the... See Moreaftereffects took longer to present themselves. While I had a slight fever, my response presented itself as bruises that itched terribly.
We are two weeks out from the vaccine, and things are going back to normal. My wife and I had to build up our stamina from the day of the shot and now (two weeks and four days ago).
Overall, we still feel that the J&J jab was the best vaccine for us. Even though this vaccine's efficacy looks less than the others, it is quite comparable if you look at the places it was tested and when it was tested.
We would highly recommend this vaccine to all who would prefer a more conventional vaccine. See Less”
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