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Olive Garden Italian Restaurant, 1925 Valley View Blvd NW, Roanoke, VA 24012, United States
Total all time reports:
1
Latest report: July 6, 2020 12:00 PM
HN
Employee test positive for Covid-19
1 year ago
An employee at Valley View Olive Garden in Roanoke tested positive for coronavirus. The employee was last at work Wednesday, June 24.
Source: wsls.com See Less
175
Related Reports
Widespread power outages affecting areas east of Peters Creek Road between Hershberger Road and Melrose Ave NW.
As of 9:40 p.m., Appalachian Power is reporting 2,296 customers are without power.
AEP reports that power will be restored by 5 a.m. on Saturday.
Source: wsls.com
Source publication date:... See More 2021 09 17 See Less
175
Power Outage, Roanoke, VA, USA
1 month ago
At least 2,300 without power in Roanoke Friday night .
Outage link: outagemap.appalachianpower.com.s3.amazonaws.com
Source: wdbj7.com
Source publication date: 2021 09 17 See Less
175
Appalachian Power hopes to have power back by 6 p.m. Thursday to a handful of customers who lost power after a crash.
Outage link: outagemap.appalachianpower.com.s3.amazonaws.com
Source: wdbj7.com
Source publication date: 2021 09 09 See Less
175
Covid-19 OSHA Complaint, Universal Logistics, 13210 Fogwell Pkwy, ROANOKE, IN, 46783, USA
1 month ago
Unsanitary conditions in the workplace, including lack of bathroom cleaning, lack of break room cleaning (microwaves, refrigerators etc), no mask wearing, no sanitizing of trucks between drivers, no social distancing, no reporting of employee illness' as related to covid exposure and poor lighting in the general area,... See More causing risks for pedestrians and staff. They are unconcerned about employee risks for exposure to covid and are not taking proper precautions.
Source: Osha.gov | Receipt Date: 2020-10-20 See Less
217
Covid-19 OSHA Complaint, Southwest Auto Sales, 7905 W County Line Rd S, ROANOKE, IN, 46783, USA
1 month ago
Employees are not wearing face coverings. No social distancing. No mask signage.
Source: Osha.gov | Receipt Date: 2021-03-10 See Less
217
Covid 19 people not properly wearing ppe. No social distancing for truck drivers. Employee people having covid and coming to work. No washing of hands ever.
Source: Osha.gov | Receipt Date: 2020-12-01 See Less
217
Covid-19 OSHA Complaint, Schewel Furniture Company Inc., 3602 Ferncliff Ave., ROANOKE, VA, 24017, USA
3 months ago
COVID-19 safety guidelines are almost completely ignored. Safety posters are present, but ignored. Management doesn't require employees or customers to wear masks or practice social distancing. Employees are not allowed to enforce mask rules with customers. Employees are told that they must work nearly every day even... See More if sick and possibly contagious. On at least two occasions, doctor's notes have been ignored by management, and employees were forced to come in to work & ignore doctor's orders. Items in the warehouse and on delivery trucks are stacked far too tall with no restraints creating a serious falling object hazard, and employees are instructed to simply pull down walls of high, heavy furniture in the interest of saving time. Fire exits in the warehouse are usually blocked by heavy merchandise. Employees operate a dangerous garbage compactor without any training or safety guidelines. Employees are not provided fully stocked first aid kits, proper PPE, or disinfectants.
Source: Osha.gov | Receipt Date: 2021-04-19 See Less
175
Covid-19 OSHA Complaint, Oak Hall Cap & Gown, 3812 Blue Ridge Drive, ROANOKE, VA, 24018, USA
4 months ago
1. Numerous employees have been out sick without any notification to ALL employees that there have been positive cases of COVID-19 in the workplace 2. Not reporting all positive cases, there are at least 8 employees sick with COVID-19 in the last two weeks.
Alleged Hazards: 2,... See More Employees Exposed: 30
Source: Osha.gov | Receipt Date: 2021-05-07 See Less
175
Covid-19 OSHA Complaint, Shakers Restaurant, 1909 Valley View Boulevard Northwest, ROANOKE, VA, 24012, USA
4 months ago
Cooks, chefs, manager, servers not wearing masks. Cooks, chefs and servers not wearing gloves.
Alleged Hazards: 1, Employees Exposed: 50
Source: Osha.gov | Receipt Date: 2021-04-15 See Less
175
Covid-19 OSHA Complaint, Papa John's #571, 2905 Brambleton Avenue, ROANOKE, VA, 24018, USA
4 months ago
Mask usage for employees has not been enforced. The employees of the store share equipment such as telephones and computers so if I am to answer the telephone I have to pick up the receiver and hold it close to my face/my mask after someone who has... See More not worn a mask appropriately or many someone's who have not been wearing mask appropriately have spoken into the receiver. Equipment is not generally sanitized between calls or usage.
Alleged Hazards: 1, Employees Exposed: 6
Source: Osha.gov | Receipt Date: 2020-11-16 See Less
175
Recent Interesting Reports
This is the 2nd package that just arrives at teterboro and just stops moving what’s the point of charging for next day air if you can’t get it done .. worse thing about this is that’s it’s anxiety medication i desperately need See Less
5.1K
HA
Hate USPS
I wonder if we could all group together and file a class action lawsuit. I saw another post here with two tracking #s stuck from October 1st and Sept 28th that haven’t moved yet.
Company name: Lupin Pharmaceuticals, Inc.
Brand name: Lupin
Product recalled: Irbesartan and Hydrochlorothiazide Tablets USP, 150mg/12.5 mg and 300mg/12.5 mg
Reason of the recall: API batches above the specification limit for the impurity, N-nitrosoirbesartan
FDA Recall date: October 14, 2021
Recall details: Baltimore, Maryland, October 14, 2021:... See More Lupin Pharmaceuticals Inc. is voluntarily recalling the below-mentioned batches of Irbesartan Tablets and Irbesartan and Hydrochlorothiazide Tablets to the consumer level. As part of Lupin’s ongoing assessment, analysis revealed that certain tested API batches (but not finished product batches) were above the specification limit for the impurity, N-nitrosoirbesartan.
Although Lupin has received no reports of illness that appear to relate to this issue, the company, out of an abundance of caution, is recalling all batches of Irbesartan Tablets USP 75mg, 150mg and 300mg and Irbesartan and Hydrochlorothiazide Tablets USP, 150mg/12.5mg and 300mg/12.5mg in the US.
Lupin discontinued the marketing of Irbesartan and Irbesartan and HCTZ tabs in Jan 2021. Risk Statement: N-nitrosoirbesartan impurity is a probable human carcinogen (a substance that could cause cancer) based on results from laboratory tests.
From October 8, 2018 (the earliest date of shipment from the manufacturing site of any of the affected batches), to September 30, 2021, Lupin received 4 reports of illness from Irbesartan and 0 reports from Irbesartan and Hydrochlorothiazide. Irbesartan tablet USP is an angiotensin II receptor blocker indicated for treatment of hypertension, to lower blood pressure, diabetic nephropathy in hypertensive patients with type 2 diabetes, an elevated serum creatinine, and proteinuria. Irbesartan Tablets USP 75mg, 150mg and 300mg is packaged in 30 and 90 count bottles and was distributed nationwide in the US to wholesalers, drug chains, mail order pharmacies and supermarkets. Lupin discontinued the marketing of Irbesartan Tablets on Jan 7, 2021. The recalled lots are included in the link below.
Irbesartan and hydrochlorothiazide tablet USP is a combination of irbesartan, an angiotensin II receptor antagonist, and hydrochlorothiazide, a thiazide diuretic, indicated for hypertension in patients not adequately controlled with monotherapy or as an initial therapy in patients likely to need multiple drugs to achieve their blood pressure goals. Irbesartan and hydrochlorothiazide tablet USP, 150mg/12.5mg and 300mg/12.5mg is packaged in 30 and 90 count bottles and was distributed nationwide in the US to wholesalers, drug chains, mail order pharmacies and supermarkets. Lupin discontinued the marketing of Irbesartan and HCTZ Tablets on Jan 7, 2021. The recalled lots are included in the link below.
Lupin Pharmaceuticals Inc. is notifying its wholesalers, distributors, drug chains, mail order pharmacies and supermarkets by phone and through recall notification and is arranging for the return of all the recalled product lots.
Patients taking, Irbesartan Tablets USP, 75mg, 150mg and 300mg and Irbesartan and Hydrochlorothiazide Tablets USP, 150mg/12.5mg and 300mg/12.5mg are advised to continue taking their medication and contact their pharmacist, physician, or medical provider for advice regarding an alternative treatment.
Wholesalers, distributors and retailers that have Irbesartan Tablets USP, 75mg, 150mg and 300mg and Irbesartan and Hydrochlorothiazide Tablets USP, 150mg/12.5mg and 300mg/12.5mg that are being recalled should discontinue distribution of the recalled product lots immediately and return it to Inmar Rx Solutions, Inc., 635 Vine St, Winston Salem, NC 27101. Tel: (855) 769-3988 / (855) 769-3989.
Consumers, wholesalers, distributors, and retailers with questions regarding this recall should contact Inmar Rx Solutions, Inc. at (855) 769-3988 / (855) 769-3989 Monday – Friday 09:00 am to 05:00 pm EST. For reimbursement, please have the recalled lots returned to Inmar Rx Solutions, Inc.; the lot number can be found on the side of the bottle label.
Check the full recall details on fda.gov
Source: FDA See Less
95
Shipment was supposed to arrive Friday. Now I received the following message : Your shipment has potentially been delayed due to emergency or other conditions at 6:46 pm on October 17, 2021. | Symptoms: Other See Less
5.1K
GR
Grinsler
Same here. Mine arrived at Teterboro 10/14 @ 3:35 pm. 10/17 update says "Processing Exception, Other Delay Your shipment has potentially been delayed due to emergency or other conditions at 6:50 pm on October 17, 2021."
MI
Fromm Four-Star Nutritionals Shredded Entrée dog food - recalled due to high Vitamin D, USA
2 weeks ago
FROMM FAMILY FOODS is issuing a voluntary recall of approximately 5,500 cases of Fromm Shredded can Entrée dog food due to potentially elevated levels of Vitamin D.
Consumers should stop feeding the products listed below to their dogs. Potential adverse reactions could occur in all size dogs. ... See More No reports of illness or injury have been reported from consumers to date, however Fromm management has determined it is prudent to pull these four lots out of distribution.
Affected recalled products were distributed at neighborhood pet stores nationwide.
Products are packaged in 12 oz. cans with Best By Date 08/2024. A full list of affected products is:
- Four-Star SHREDDED BEEF IN GRAVY ENTRÉE food for dogs, 12 cans per case, 11877, 12 oz. per can, UPC: 7270511876, Best By Date 082024
- Four-Star SHREDDED CHICKEN IN GRAVY ENTRÉE food for dogs, 12 cans per case, 11881, 12 oz. per can, UPC: 7270511880, Best By Date 082024
- Four-Star SHREDDED CHICKEN IN GRAVY ENTRÉE food for dogs, 12 cans per case, 11879, 12 oz. per can, UPC: 7270511878, Best By Date 082024
-Four-Star SHREDDED TURKEY IN GRAVY ENTRÉE food for dogs, 12 cans per case, 11883, 12 oz. per can, UPC: 7270511882, Best By Date 082024
Dogs ingesting elevated levels of Vitamin D may exhibit symptoms such as vomiting, loss of appetite, increased thirst, increased urination, excessive drooling, and weight loss. Vitamin D when consumed at very high levels can lead to serious health issues in dogs including renal dysfunction. Consumers who have dogs that have consumed any of the affected products and are exhibiting these symptoms should contact their veterinarian.
Check the full recall details on fda.gov
Company name: Fromm Family Foods
Brand name: Fromm Four-Star Nutritionals
Product recalled: Shredded Entrée canned dog food
Reason of the recall: Elevated levels of Vitamin D
FDA Recall date: October 01, 2021
Source: FDA See Less
95
USPS Lost package, USPS Teterboro Distribution Center, Industrial Avenue, Teterboro, NJ, USA
3 days ago
USPS lost yet another package at their Teterboro distribution center, reporting "Processing Exception Delay" with no way to know if it will be resolved or not. See Less
5.1K
A few weeks ago. My cat got sick from food delivered by chewy. It sat on the porch in the sun. It is wet food. We noticed the color was off but didn’t think it could make him so sick. I had to take him to the... See More vet twice for vomiting and not eating after 1 can. I emailed chewy and sent pictures. They refunded my money and I will only go to the pet store for food for now on. | Symptoms: Nausea, Vomiting See Less
3.7K
Priority mail packages bouncing up and down the east coast unnecessarily for days, 4 days later my package is further away from being delivered than when it started. Please fire the guy running this sh*t show. See Less
5.1K
Company name: Cook Medical
Brand name: Cook Medical
Product recalled: Transseptal Needle and Transseptal Needle Catheter
Reason of the recall: Complaints of rust on the products
FDA Recall date: October 19, 2021
Recall details: Bloomington, Ind. — On October 8, 2021, Cook Medical issued a global, voluntary... See More recall of the Transseptal Needle and the Transseptal Needle with Catheter. This recall includes all unexpired lots for both of these products. The needles were recalled due to complaints of rust on the products. Use of affected products could result in increased procedural time and inflammatory reactions, including systemic reactions which may lead to permanent impairment or death.
The U.S. Food and Drug Administration (FDA) has not yet classified the recall. Products affected by this recall are:
- Transseptal Needle, INTENDED USE: Intended for transseptal left heart access in both diagnostic and interventional procedures, RPN: TSNC-18-71.0 GPN: G02364 and RPN: TSNC-19-56.0 GPN: G02365, all lot numbers, RANGE OF MANUFACTURE DATES FOR AFFECTED PRODUCTS: October 02, 2016 through July 22, 2021
- Transseptal Needle with Catheter, INTENDED USE: Intended to facilitate transseptal entry into the left atrium, RPN: TSN-17-75.0-ENDRYS, GPN: G19261, all lot numbers, RANGE OF MANUFACTURE DATES FOR AFFECTED PRODUCTS: October 02, 2016 through July 22, 2021
Transseptal Needles, including Transseptal Needles with Catheters, were found to have rust internally, externally, or both. To date, Cook Medical has received no reports of injury or illness related to this recall. Cook has received four complaints where the presence of rust was identified prior to patient contact. However, please be advised that the presence of rust may go undetected by the user. The FDA and other regulatory agencies around the world have been notified of this action.
Potential adverse events: If an affected product is used, potential negative outcomes include increased procedural time (to obtain a replacement device) and inflammatory reactions ranging from local or self-limited reactions to systemic reactions requiring medical intervention. Systemic reactions could potentially lead to permanent impairment or death.
Check the full recall details on fda.gov
Source: FDA See Less
95
Company name: Bryant Ranch Prepack
Brand name: Bryant Ranch Prepack
Product recalled: Methocarbamol 500mg
Reason of the recall: Bottles labeled as Methocarbamol 500mg tablets were found to contain Methocarbamol 750mg tablets.
FDA Recall date: October 19, 2021
Recall details: Burbank, CA, Bryant Ranch Prepack is voluntarily recalling... See More 1 lot of Methocarbamol 500mg, Tablets to the consumer level. The bottles labeled as Methocarbamol 500mg Tablets have been found to contain Methocarbamol 750mg Tablets.
Risk Statement: If a patient takes a 750mg Tablet of Methocarbamol instead of the prescribed 500mg Tablets, it potentially could result in Excessive Central Nervous System depression which may result in nausea, sedation, fainting, falls, seizure, coma, and death. Bryant Ranch Prepack has not received any reports of adverse events related to this recall.
The product is used together with rest, physical therapy, and other measures for the relief of discomfort associated with acute, painful musculoskeletal conditions and is packaged in a white round bottle with a red and white label, which reads Methocarbamol 500mg packaged in counts of 30 (NDC:7133517952), 60 (NDC: 7133517954), and 90 (NDC:7133517957) pills. The affected Methocarbamol 500mg lots include the following Lot Number 163935/ Exp. Date 10/22. The product can be identified by red and white label with a yellow border at the top and bottom of the label, top of the label reads “Packaged by Bryant Ranch Prepack”, labels are pictured below. The Methocarbamol 500mg was distributed Nationwide to multiple physician offices.
Bryant Ranch Prepack is notifying its distributors and customers by letter and email and is arranging for return of all recalled products. Consumers that have the bottles labeled as Methocarbamol 500mg Tablets which is being recalled should stop using immediately and return to place of purchase and/or contact their physician. Distributors/Physicians should stop distribution and contact Bryant Ranch Prepack to return the product immediately.
Check the full recall details on fda.gov
Source: FDA See Less
95
It’s been over 20 days for next-state packages and still have not arrived. See Less
5.1K