Ralphs, 10901 Ventura Blvd, Studio City, CA 91604, USA
Latest report:
Covid-19 OSHA Complaint
3 years ago
Look Article 10: PPE requirements for General Industry: 3380(a), and 3384(a) Also look for §5199. Aerosol Transmissible Diseases. Complainant states, ¿Store too crowded and not being monitored check stands not being sanitized every half hour . They are letting customers with no mask in to buy groceries
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and not saying anything to them . We have almost 200 employees so all employees who are scheduled to work are exposed on a daily basis¿
Alleged Hazards: 2,
Source: Osha.gov | Receipt Date: 2020-04-26
Alleged Hazards: 2,
Source: Osha.gov | Receipt Date: 2020-04-26
981
Covid-19 OSHA Complaint
3 years ago
Look Article 10: PPE requirements for General Industry: 3380(a), and 3384(a) Also look for §5199. Aerosol Transmissible Diseases. Complainant states, ¿This store is not following CDC guidelines and is allowing as many people in the store at a time until it reaches a critical amount and only
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then takes action. Today Saturday 4/24 at 245 pm the store became way overcrowded and only after several employees and customers complained did they close the door. There is such constant business that check stands are not being sanitized. Employees are not washing there hands every 30 minutes. Only on lunch or break. Signs are up stating carts are sanitized yet they are none be cleaned. Bathrooms are not being cleaned or sanitized every 1/2 hour. The store is the only location where they are not limiting the number of people allowed in the store. They are more interested in reaping in more sales and do not care about the health of the employees.¿ T8 CCR 3203(a)(4)(6)/ Employer is allowing too many people in without masks overcrowding the store and employees are working closer than 6 feet of others in violation of CDC COVID-19 infection control procedures. T8 CCR 3362, 3380(f)/ Check stands are carts are not being sanitized and bathrooms are not being cleaned and sanitized. Employees are not washing their hands.
Source: Osha.gov | Receipt Date: 2020-04-25
Source: Osha.gov | Receipt Date: 2020-04-25
981
Covid-19 OSHA Complaint
3 years ago
1. The employer is not enforcing customers to wear facial covering.
2. Employees are not protected by plastic barrier at the self-checkout stands. Customers buying alcohol at the self-checkout stand have to take out their mask to verify their age resulting in exposure to employees.
3. Employer …
2. Employees are not protected by plastic barrier at the self-checkout stands. Customers buying alcohol at the self-checkout stand have to take out their mask to verify their age resulting in exposure to employees.
3. Employer …
has not develop a system and procedures to maintain six feet distances among customers and employees.
4. Employer lets everyone come in the store at the same time.
Alleged Hazards: 2,
Source: Osha.gov | Receipt Date: 2020-04-20
4. Employer lets everyone come in the store at the same time.
Alleged Hazards: 2,
Source: Osha.gov | Receipt Date: 2020-04-20
981
Recent Interesting Reports
Online Scam, NJ, USA
3 weeks ago •reported by user-vqqn8125
I ordered a device for unlimited Internet and received a adapter of some some sort. It was from Heathers MOTTY 2207 Summit Ave. Union City NJ 07087. I ordered internet device to receive unlimited Internet. They sent an adapter.
272
Unsolicited purchase, Sarasota, FL, USA
1 week ago •reported by user-qgrvz545
I received a USPS package or something Keto Puree that I didn't buy
178
The sender is LINGXIA HONG KONG RO, Romania
1 week ago •reported by user-jzyn5715
We ordered on the internet a device that they said measures diabetes without stinging, blood pressure and blood oxygen levels... say 3 in 1 at the price of 190 lei + 20 lei transport. Big wonder... it is a machine pin with a stinging device... of poor quality
10
AuroMedics Pharma Methocarbamol Injection - recalled due to Particulate Matter presence, USA
4 weeks ago •source www.fda.gov
Recall notice
Eugia US LLC (f/k/a AuroMedics Pharma LLC) has initiated a voluntary recall of lot number 3MC23011 of Methocarbamol Injection, USP 1000 mg/10 mL (100mg/mL) (Single Dose Vial) - 10mL Vial to the consumer level due to a customer product complaint for the presence of white particles floating
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inside of the vial.
Administration of an injectable product that contains particulate matter may result in local irritation or swelling. If the particulate matter reaches the blood vessels or is injected intravascularly it can travel to various organs and block blood vessels in the heart, lungs or brain which can cause stroke and even lead to death. To date, Eugia US LLC has not received any reports of adverse events related to this recall.
Methocarbamol injection USP 1000 mg/10 mL (100mg/mL), is used as an adjunct to rest, physical therapy, and other measures for the relief of discomfort associated with acute, painful musculoskeletal conditions. It is packaged in 10 mL and packed as 25 (vials) X 04 (Printed E-Flute cartons) X 01 (Shipper) with NDC code as 55150-223-10. Eugia US LLC shipped the entire lot to wholesalers nationwide from Jan 12, 2024, through Jan 16, 2024.
The product can be identified by product name on carton and vial label and with lot number 3MC23011 and Exp. Date: Nov 2026 (NDC 55150-223-10) (See enclosed vial label). The product label is as shown in the image below.
Eugia US LLC (f/k/a AuroMedics Pharma LLC) is notifying its distributors by recall letters and is arranging for the return/replacement of all recalled products. Wholesalers, hospitals, pharmacies, institutions, and doctors with an existing inventory of the recalled product lot should discontinue use, stop distribution and quarantine the product immediately. If you have further distributed the recalled product lot, notify your accounts and/or any additional locations which may have received the recalled product. Hospitals/Institutions should inform Healthcare Professionals in your organization of this recall.
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.
If you are experiencing any harm after using this product it is important to report it. It can help to detect & resolve outbreaks early and prevent others from being harmed, and it enables better surveillance. If symptoms persist seek medical attention.
Company name: Eugia US LLC
Brand name: Eugia US LLC
Product recalled: Methocarbamol Injection, USP 1000 mg/10 mL (100mg/mL) (Single Dose Vial)
Reason of the recall: Device & Drug Safety – Presence of Particulate Matter
FDA Recall date: March 28, 2024
Source: www.fda.gov
Administration of an injectable product that contains particulate matter may result in local irritation or swelling. If the particulate matter reaches the blood vessels or is injected intravascularly it can travel to various organs and block blood vessels in the heart, lungs or brain which can cause stroke and even lead to death. To date, Eugia US LLC has not received any reports of adverse events related to this recall.
Methocarbamol injection USP 1000 mg/10 mL (100mg/mL), is used as an adjunct to rest, physical therapy, and other measures for the relief of discomfort associated with acute, painful musculoskeletal conditions. It is packaged in 10 mL and packed as 25 (vials) X 04 (Printed E-Flute cartons) X 01 (Shipper) with NDC code as 55150-223-10. Eugia US LLC shipped the entire lot to wholesalers nationwide from Jan 12, 2024, through Jan 16, 2024.
The product can be identified by product name on carton and vial label and with lot number 3MC23011 and Exp. Date: Nov 2026 (NDC 55150-223-10) (See enclosed vial label). The product label is as shown in the image below.
Eugia US LLC (f/k/a AuroMedics Pharma LLC) is notifying its distributors by recall letters and is arranging for the return/replacement of all recalled products. Wholesalers, hospitals, pharmacies, institutions, and doctors with an existing inventory of the recalled product lot should discontinue use, stop distribution and quarantine the product immediately. If you have further distributed the recalled product lot, notify your accounts and/or any additional locations which may have received the recalled product. Hospitals/Institutions should inform Healthcare Professionals in your organization of this recall.
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.
If you are experiencing any harm after using this product it is important to report it. It can help to detect & resolve outbreaks early and prevent others from being harmed, and it enables better surveillance. If symptoms persist seek medical attention.
Company name: Eugia US LLC
Brand name: Eugia US LLC
Product recalled: Methocarbamol Injection, USP 1000 mg/10 mL (100mg/mL) (Single Dose Vial)
Reason of the recall: Device & Drug Safety – Presence of Particulate Matter
FDA Recall date: March 28, 2024
Source: www.fda.gov
304
Received a ring that I didn’t order, 44211 Lancaster Boulevard, Lancaster, CA 93535, USA
3 weeks ago •reported by user-fbzf1817
I received a ring that I didn’t order. I’m going to return it.
Feathers Fottys is an absolute scam, Michigan, USA
2 weeks ago •reported by user-whnhc378
Feathers Fottys is an absolute scam. The product is cheaply made with no instructions at all. Ordered the neck beauty device. It’s a joke but I am reporting their scam.
The promo on Facebook was made to look so promising for turkey neck issues and facial wrinkles. …
The promo on Facebook was made to look so promising for turkey neck issues and facial wrinkles. …
I ordered the product which took forever to get here. The product came in a nondescript I’ve box with absolutely no instructions on how to use it and no return instructions. There isn’t even contact info.
198
I didn't order this package, Saarlouis, Deutschland
2 weeks ago •reported by user-cwxk5889
I received a package from DHL Parcel Returns (YW) that I did not order 😡
What to do?? Can anyone help?
What to do?? Can anyone help?
12
I recieve this bottle, McComb, MS, USA
1 week ago •reported by user-mzjwb374
Came in a white package
15
A package I never ordered, Detroit, MI, USA
1 week ago •reported by user-xyhyr989
I received a package from an address in Inglewood cali I never ordered
484
Scam, Salem, IN, USA
3 weeks ago •reported by user-fpprv682
Received Dietary supplement from Subgenix. I did Not order this product. They charged my account around $200.
Small bottle in plastic mailing envelope. Return address is:
Fulfillment House
PO Box 5708
Tampa, Fl 33675-5708
Small bottle in plastic mailing envelope. Return address is:
Fulfillment House
PO Box 5708
Tampa, Fl 33675-5708
7
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