Source: Osha.gov | Receipt Date: 2021-10-29
Report by
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Product: Onion
Updated:
Source: Osha.gov | Receipt Date: 2021-10-29
Covid-19 OSHA Complaint, Royal Fresh Cuts, Inc, 3675 Zip Industrial Blvd, ATLANTA, GA, 30354, USA
3 years ago
Source: Osha.gov | Receipt Date: 2020-12-14
Source: www.burlingtonfreepress.com
5. Procedures for responding to vomiting and diarrheal events
- comments: observed no clean-up items (disposable apron,twist tie garbage bags,disposable mop,absorbent)for vomiting and diarrhea. Must provide and maintain. (priority foundation 7-38-005)
22. Proper cold holding temperatures
- comments: observed improper temperatures of
25. Consumer advisory provided for raw/undercooked food
- comments: observed no consumer advisory disclosure and reminder on menu of consuming raw and under cooked foods(eggs). Must provide and maintain. (priority foundation 7-38-005)
33. Proper cooling methods used; adequate equipment for temperature control
- comments: observed glass sliding reach in cooler at 54. 3f with tcs foods stored inside for sale in front prep area. A held for inspection tag placed on unit. Once repaired fax or email letter when ready. Must have cold holding unit at 41. 0f or below. (priority 7-38-005)
36. Thermometers provided & accurate
- comments: must provide a thermometer for 1- door glass reach in cooler.
37. Food properly labeled; original container
- comments: must label food storage container when food is not in original package.
38. Insects, rodents, & animals not present
- comments: observed evidence of appx. 100 or more mice droppings on floor next to front sliding glass reach in cooler,under 2- door storage reach in cooler and 1- door prep cooler,under drainboard at 3- comp sink,behind hot water tank,under both chest freezers,in toilet room next to vanity. Inside ledges of unused 3- door reach in cooler in rear area. Must remove droppings. Clean and sanitize areas. Recommended to have a pest control operator to service premises on or after 6/8/2020. (priority foundation 7-38-020(a)
38. Insects, rodents, & animals not present
- comments: observed an appx. '1/2-3/4' gap along bottom of lobby(east) door and torn / worn screen at rear door. Must repair or replace.
47. Food & non-food contact surfaces cleanable, properly designed, constructed & used
- comments: must repair or replace worn door gaskets on both chest freezers.
49. Non-food/food contact surfaces clean
- comments: must clean grease and food debris build up from grill table,prep table,reach in cooler & prep cooler,fryer cabinets. Must defrost chest freezers.
53. Toilet facilities: properly constructed, supplied, & cleaned
- comments: must repair or replace broken self closing device on toilet room door that leads into rear prep area.
55. Physical facilities installed, maintained & clean
- comments: must clean dirt and food debris build up from walls in front prep area and toilet room.
55. Physical facilities installed, maintained & clean
- comments: must repair or replace stained ceiling tiles in lobby area,loose floor tiles near hot water tank,excessive caulk at hole in wall behind toilet & missing wall bases in toilet room.
56. Adequate ventilation & lighting; designated areas used
- comments: must repair or replace cracked light shield in front prep area,missing light shields in rear prep/dish washing area and replace burnt out lights in same areas.
Source: chicago.gov
Recent Interesting Reports
AvKARE, LLC Atovaquone Oral Suspension - recalled due to potential Bacillus cereus contamination, USA
3 weeks ago •source www.fda.gov
Recall notice
Risk Statement: In the population most at risk, immunocompromised population, there is a reasonable probability that microbial contamination of Atovaquone Oral Suspension can result in disseminated, life threatening infections such as endocarditis and necrotizing soft tissue infections.
Atovaquone Oral Suspension, USP is indicated for prevention and treatment of Pneumocystis jiroveci pneumonia (PCP) in adults and children 13 years of age and older who cannot tolerate other medicines, such as trimethoprim-sulfamethoxazole.
The product is packaged in a carton. The identified NDC # associated with the product is 50268-086-12, UPC # 5026808612 and the affected lot# is AW0221A with an expiration date of 08/2025.
AvKARE, LLC is notifying its distributors and wholesale customers by mailings and email communications method and is arranging for returns of all recalled Atovaquone Oral Suspension, USP. Wholesalers who have Atovaquone Oral Suspension, USP 750mg/5mL, which are being recalled, should examine their inventory and cease dispensing, return any of the impacted lots to AvKARE, LLC. Consumers that have product which is being recalled should stop using the product and return it to place of purchase.
This recall is being conducted with the knowledge of the U.S. Food and Drug Administration.
In case you experience harm from this product, it is important to report it. It can help to detect & resolve issues and prevent others from being harmed, and it enables better surveillance. If symptoms persist, seek medical care.
Company name: AvKARE, LLC
Brand name: AVpak
Product recalled: Atovaquone Oral Suspension, USP 750mg/5mL
Reason of the recall: Potential Bacillus cereus contamination
FDA Recall date: April 01, 2024
Source: www.fda.gov
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ForeverMen Natural Energy Boost - recalled due to undeclared allergens, USA
3 weeks ago •source www.fda.gov
Recall notice
Risk Statements: Men with diabetes, high blood pressure, high cholesterol, or heart disease, may be on medications that if taken with these products could lower blood pressure to dangerous levels that could be life threatening. The products affected are men with diabetes, high blood pressure, high cholesterol, or heart disease.
The product is marketed as dietary supplements for male sexual enhancement and is packaged in a blister card. 10 count box. We are notifying the public through this public announcement due to lack of ability to identify customers who may have received the product. FAonline INC. is notifying its customers that have the ForeverMen products to stop use and properly discard the product.
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.
In case you experienced harm from allergens or undeclared ingredients, it is important to report it. It can help to detect & resolve issues and prevent others from being harmed, and it enables better surveillance. If symptoms persist, seek medical care.
Company name: FAonline Inc
Brand name: ForeverMen
Product recalled: Natural Energy Boost
Reason of the recall: Product is tainted with sildenafil and tadalafil
FDA Recall date: April 02, 2024
Source: www.fda.gov
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I ordered hooks and rods
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Heather Fottys
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