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Rubio's
Updated: October 13, 2020 12:00 PM
Covid-19 OSHA Complaint, Rubio's, 1500 N Green Valley Pkwy, Henderson, NV 89074, United States
Rubio's, 1500 N Green Valley Pkwy, Henderson, NV 89074, United States
October 13, 2020 12:00 PM
“1. The employer is not complying with the Governor?s COVID-19 guidelines. Employees testing positive for COVID-19 are asked to return to work after a confirmed case.
2. The facility is not being cleaned or disinfected following an employee testing positive.
Hazard Location:
Throughout.
7/17... See More/2020
bb
Alleged Hazards: 2,
Source: Osha.gov | Receipt Date: 2020-07-13 See Less”
Helpful
Covid-19 OSHA Complaint, Rubio's, 1500 North Green Valley Parkway, Henderson, Nevada 89074, USA
Rubio's, 1500 North Green Valley Parkway, Henderson, Nevada 89074, USA
September 17, 2020 12:00 PM
“1. The General Manager stated to all employees that an employee tested positive for Covid-19, and that they had submitted paperwork for clearance so that the employee could return to work. Employees were informed by the returning employee that they had only received their positive results the same d... See Moreay as the when they began working again. Employees are concerned that the Employer and management staff are not handling the situation well, and that they have been exposed to Covid-19.
HAZARD LOCATION:
Throughout
7/28/2020
JH
Alleged Hazards: 1, Employees Exposed: 1
Source: Osha.gov | Receipt Date: 2020-07-13 See Less”
Helpful
Covid-19 OSHA Complaint, Rubio's, 1500 North Green Valley Parkway, Henderson, Nevada 89074, USA
Rubio's, 1500 North Green Valley Parkway, Henderson, Nevada 89074, USA
September 7, 2020 12:00 PM
“1. An employee has tested positive for Covid-19. Management has scheduled and enforced that the employee continue working, and other employees are concerned that they will be exposed to Covid-19 under these working conditions.
Hazard Location:
Throughout the facility.
07/12/2020
DG
All... See Moreeged Hazards: 1,
Source: Osha.gov | Receipt Date: 2020-07-12 See Less”
Helpful
Covid-19 OSHA Complaint, Rubio's, 1500 North Green Valley Parkway, Henderson, NV, USA
Rubio's, 1500 North Green Valley Parkway, Henderson, NV, USA
September 7, 2020 12:00 PM
“1. Employees have concerns that a co-worker tested positive on July 8, 2020 for Covid-19 and was placed back onto the work schedule and worked the following day.
Hazard Location:
Throughout.
07/13/2020
DG
Alleged Hazards: 1, Employees Exposed: 1
Source: Osha.gov | Receipt Date: 2020-... See More07-13 See Less”
Helpful
Recent Interesting Reports
December 31, 2020 11:24 AM
“Responding to an add on facebook I ordered and paid for a battery powered chainsaw on Dec. 13. I then received a confirmation email. On Dec. 30 I received an envelope the size of a cigarette pack containing a manual chainsaw. Where are the fact checkers when you need them? See Less”
Helpful
2 people found this review helpful
Cat food cans had been expired, SuperFresh Glen Rock, Lincoln Avenue, Glen Rock, NJ, USA
SuperFresh Glen Rock, Lincoln Avenue, Glen Rock, NJ, USA
January 3, 2021 5:22 AM
“I bought 9lives canned cat food and 3 of 4 cans had been expired from 11/11/19. Their store is not offering refunds but if I had not looked at the date my cats would have got sick See Less”
Helpful
1 person found this review helpful
Blackcass woodcutter battery operated saw, Chico, CA, USA
Chico, CA, USA
January 25, 2021 3:00 PM
“I ordered what I thought was a Skihl brand chainsaw and got a piece of crap chainsaw that was defective and dangerous to use as it fell apart easily. When you put it down the chain fell off. The guard didnt fit the chain. And just a very dangerous tool See Less”
Helpful
December 30, 2020 10:00 PM
“Company name: Sportmix
Brand name: Sportmix
Product recalled: Dog and Cat Food
Reason of the recall: Elevated levels of aflatoxin
FDA Recall date: December 30, 2020
Recall details: Midwestern Pet Foods, Inc., of Evansville, IN is issuing a voluntary recall of the below-listed dog and cat food p... See Moreroducts due to tests indicating levels of Aflatoxin that exceed acceptable limits. Products were distributed nationally to online distributors and retail stores. Aflatoxin is a toxin produced by the mold Aspergillus flavus, which can grow on corn and other grains used as ingredients in pet food. At high levels, aflatoxin can cause illness and death in pets.
There have been reports of illnesses and deaths in dogs associated with the below listed lots of Sportmix High Energy. No cat or human illnesses have been reported. If your pet shows signs of aflatoxin poisoning including sluggishness, loss of appetite, vomiting jaundice (yellowish tint to the eyes, gums, or skin due to liver damage), and/or diarrhea, contact a veterinarian immediately. Provide a full diet history to your veterinarian. It may be helpful to take a picture of the pet food label, including the lot number. Lot code information may be found on the back of the bag and will appear in a three-line code, with the top line in the format “EXP 03/03/22/05/L#/B###/HH:MM” as follows (see below in pictures section).
Retailers and distributors should immediately pull recalled lots from their inventory and shelves. Do not sell or donate the recalled products. Retailers are encouraged to contact consumers who have purchased the recalled products if you have the means to do so (frequent buyer cards, etc.).
Pet parents: do not feed the recalled products to your pets or any other animals. Destroy the products in a way that children, pets, and wildlife cannot access them. Wash and sanitize pet food bowls, cups, and storage containers. Contact Midwestern Pet Foods Consumer Affairs at 800-474-4163, ext. 455 from 7AM to 4PM Central Time, Monday through Friday, or by email at info@midwesternpetfoods.com for additional information. This is a voluntary recall conducted in cooperation with the U.S. Food and Drug Administration.
Recalled lot codes are as follows:
- 50# Sportmix Energy Plus Lots Exp 03/02/22/05/L2, 03/02/22/05/L3, 03/03/22/05/L2
- 44# Sportmix Energy Plus Lots 03/02/22/05/L3
- 50# Sportmix Premium High Energy Lots 03/03/22/05/L3
- 44# Sportmix Premium High Energy Lots 03/03/22/05/L3
- 31# Sportmix Original Cat Lots 03/03/22/05/L3
- 15# Sportmix Original Cat Lots 03/03/22/05/L2, 03/03/22/05/L3
Products may be identified as follows (see pictures below).
Check the full recall details on fda.gov
Source: FDA See Less”
Helpful
January 25, 2021 7:00 PM
“Company name: Nostrum Laboratories, Inc.
Brand name: Nostrum Laboratories, Inc.
Product recalled: Metformin HCl Extended Release Tablets, USP 750 mg
Reason of the recall: Due to levels of nitrosamine impurities above the ADI limit of 96 ng/day
FDA Recall date: January 25, 2021
Recall details: K... See Moreansas City, Missouri,Nostrum Laboratories, Inc. is voluntarily recalling one lot of Metformin HCl Extended Release Tablets, USP 750 mg (generic equivalent to Glucophage Tablets) to the consumer level. The Metformin HCl Extended Release Tablets, USP 750 mg (generic equivalent to Glucophage Tablets) have been found to contain levels of nitrosamine impurities above the ADI limit of 96 ng/day, as published in the FDA Guidance Document issued September 2020. This is an expansion of the recall initially announced on November 2nd 2020. NDMA is classified as a probable human carcinogen (a substance that could cause cancer) based on results from laboratory tests.
NDMA is a known environmental contaminant and found in water and foods, including meats, dairy products, and vegetables. To date, Nostrum Laboratories, Inc. has not received any reports of adverse events related to this recall.
The product is indicated as an adjunct to diet and exercise to improve blood glucose control in adults with type 2 diabetes mellitus and is packaged in HDPE bottles of 100 tablets, under NDC 29033-056-01. The affected Metformin HCl Extended Release Tablets, USP 750 mg (generic equivalent to Glucophage Tablets) lot is listed in the table below. The product can be identified as an off-white oblong tablet debossed with “NM7”. Metformin HCl Extended Release Tablets, USP 750 mg (generic equivalent to Glucophage Tablets) was distributed Nationwide in the USA to wholesalers who further distributed to pharmacies and patients.
- Product Description: Metformin HCl Extended Release Tablets, USP 750 mg (generic equivalent to Glucophage Tablets)
- NDC: 29033-056-01
- Lot Number: MET200601
- Expiry Dates: 07/2022
Nostrum Laboratories, Inc. is notifying its distributors by letter and is arranging for return of all recalled products. Consumers with medical questions regarding this recall can contact Nostrum Laboratories, Inc. Medical Affairs at phone number 816-308-4941 or email quality@nostrumpharma.com Monday through Friday from 8 am – 5 pm CST. Consumers should contact their physician or pharmacy for further medical advice.
Check the full recall details on fda.gov
Source: FDA See Less”
Helpful
Misleading advertisement and fraudulent company, St. George, UT, USA
St. George, UT, USA
January 7, 2021 7:57 PM
“I purchased the portable carbon steel chain from Blackcass. When going to their site, It looks like you are getting the Chain saw and are advertising it for $29.99 When in reality you are purchasing the chain for $29.99. They do advertise that you are getting the chain and not the chainsaw, but m... See Moreake it look like you are getting the saw. When you look at the ad it is very deceiving. I do realize that I did not pay attention when I pushed the buy button. They do say 100% money back guarantee, but do not honor that when you try to return the item. I keep contacting the company. First they offered me the saw at a discount price. Second they offered me 10% of my money back. Then 12% then 15% twice. They keep saying that not to return the item until they give me the return address. They have not yet sent me the return address. I have a friend that says they wait to send me the return address until it is too late to send it to them because they give you 30 days to return the item. They have not yet sent me the address. I just want to send it back. I have contacted paypal and they say there is nothing they can do. I have contacted yt network technology which is the company that paypal says I purchased the item from. I have only heard from them 1 time and sent them the information that they asked for, but have not heard back. What do I do? Can this company be stopped? See Less”
Helpful
2 people found this review helpful
Moderna COVID-19 Vaccine, no symptoms yet., Long Island City, Queens, NY, USA
Long Island City, Queens, NY, USA
January 14, 2021 8:51 PM
“I am a teacher and am authorized to get the Moderna vaccine. I made an appointment in Ridgewood 2 days ago. Appoint was at 5:20 but didn't get my shot until 7:40. The lines are extremely long at night. But the nurse said they are empty in the morning. Once you get inside it is very fast, everyone is... See Morevery helpful and you can sign up for your second vaccine. They make you wait 15 mins to make sure you're ok before you leave. I have no side effects from the shot and feel fine. See Less”
Helpful
3 people found this review helpful
Dream bones have made both of my dogs sick, Tracy, CA, USA
Tracy, CA, USA
January 21, 2021 4:42 PM
“I fed both my dogs a chicken wrapped dream See Less”
Helpful
3 people found this review helpful
Moderna COVID-19 vaccine, Sevierville, TN, USA
Symptoms: Headache
Chills
Fatigue
Joint Pain
Muscle Pain
Soreness
Sevierville, TN, USA
January 22, 2021 1:14 PM
“Moderna first vaccine 12/23/20. Arm felt sore a little worse than a tetanus shot. Felt pretty fatigued the next two days afterwards. Second Moderna vaccine 01/20/21. Arm felt sore pretty much within a couple of hours. The next day had hot/cold chills, muscle/joint pain and headache. The 2nd day my... See Moreinjection site was red/warm to touch and has spread quite a bit. Showed the Covid screeners and they said that this is common after the 2nd shot. Took Tylenol and will continue to watch. See Less”
Helpful
3 people found this review helpful
January 8, 2021 6:01 PM
“Company name: Fresenius Kabi USA
Brand name: Fresenius Kabi
Product recalled: Ketorolac Tromethamine Injection, USP, 30 mg/mL
Reason of the recall: Presence of particulate matter
FDA Recall date: January 08, 2021
Recall details: Fresenius Kabi USA is voluntarily recalling a single lot of Ketoro... See Morelac Tromethamine Injection, USP, 30 mg/mL, 1 mL fill in a 2 mL amber vial to the user level due to the presence of particulate matter. Particulate matter was found in reserve sample vials. No adverse event reports have been received for the recalled lot, which was produced and sold in 2019.
Administration of products containing particulate matter could obstruct blood vessels and result in local irritation of blood vessels, swelling at the site of injection, a mass of tissue that could become inflamed and infected, blood clots traveling to the lung, scarring of the lung tissues, and allergic reactions that could lead to life-threatening consequences.
Ketorolac Tromethamine, a nonsteroidal anti-inflammatory drug, is indicated for the short-term (up to 5 days in adults) management of moderately severe acute pain that requires analgesia at the opioid level. The total combined duration of use of oral Ketorolac Tromethamine and Ketorolac Tromethamine Injection should not exceed 5 days. Listed below is a table of the recalled lot distributed nationwide in the United States to wholesalers, distributors, hospitals, and pharmacies between March 28, 2019 and September 3, 2019.
Product Name/Product size: Ketorolac Tromethamine Injection, USP, 30mg / mL, 1 mL fill in a 2 mL amber vial
NDC Number: 63323-162-01
Product Code: 160201
Batch Number: 6121083
Expiration Date: 02/2021
First Ship Date: 03/28/2019
Last Ship Date: 09/03/2019
Fresenius Kabi is notifying its distributors and customers by letter and asking customers and distributors to check their stock immediately and to quarantine and discontinue the use and distribution of any affected product. Distributors should notify their customers and direct them to quarantine and discontinue distributing or dispensing the affected lot, and to return the product to Fresenius Kabi.
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
2 people found this review helpful