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IMPORTANT - YOUR REPORT IS QUEUED - IT MAY TAKE UP TO 12 HOURS FOR YOUR REPORT TO SHOW ON OUR HOME PAGE (IF NOT OPTED AS PRIVATE)

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Visit our learn pages for more helpful information or, email us: support@safelyhq.com

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Ralphs

Updated: January 4, 2021 5:55 PM

January 4, 2021 5:55 PM

“A woman sick with Covid was forced back to work while testing positive. She works with customers and fruits and vegetables. The store manager made her come bavk. Disgusting See Less
Reported By SafelyHQ.com User

Covid-19 OSHA Complaint, Ralphs, 14400 Culver Drive, IRVINE, CA, 92604, USA

Ralphs, 14400 Culver Drive, IRVINE, CA, 92604, USA

December 9, 2020 12:00 PM

Ҥ3380 Employees not trained to use Personal Protective Equipment and employees are not using their masks and gloves correctly.

Alleged Hazards: 1, Employees Exposed: 3
Source: Osha.gov | Receipt Date: 2020-04-28 See Less
Reported By SafelyHQ.com User

Covid-19 OSHA Complaint, Ralphs, 380 E 17th St, COSTA MESA, CA, 92627, USA

Ralphs, 380 E 17th St, COSTA MESA, CA, 92627, USA

December 2, 2020 12:00 PM

“Mask order not being enforced.

Alleged Hazards: 1, Employees Exposed: 1
Source: Osha.gov | Receipt Date: 2020-06-29 See Less
Reported By SafelyHQ.com User

Covid-19 OSHA Complaint, Ralphs, 10901 Ventura Blvd, Studio City, CA 91604, USA

Ralphs, 10901 Ventura Blvd, Studio City, CA 91604, USA

November 25, 2020 12:00 PM

“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 then tak... See Morees 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
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Reported By SafelyHQ.com User

Covid-19 OSHA Complaint, Ralphs, 10901 Ventura Blvd, Studio City, CA 91604, USA

Ralphs, 10901 Ventura Blvd, Studio City, CA 91604, USA

November 25, 2020 12:00 PM

“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 grocer... See Moreies 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
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Reported By SafelyHQ.com User

Covid-19 OSHA Complaint, Ralphs, Sunset Boulevard, Los Angeles, CA 90046, USA

Ralphs, Sunset Boulevard, Los Angeles, CA 90046, USA

November 25, 2020 12:00 PM

“T8CR §§3203(a), 3380(f), 5141 Employer is not ensuring safe physical distancing to prevent the spread of Novel Coronavirus. Employees are not provided with proper PPE when the need to sanitize the store where employees have tested positive for Novel Coronavirus and have contracted COVID-19 have work... See Moreed. The employer does not ensure safe physical distancing where instacart employees work in the store. The employer has not tested other employees for Novel Coronavirus infection and 21 employees have contracted COVID-19. When employees come to work sick, they are not sent home.


Source: Osha.gov | Receipt Date: 2020-04-30
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Reported By SafelyHQ.com User

Covid-19 OSHA Complaint, Ralphs, 1200 N Central Ave, Glendale, CA 91202, United States

Ralphs, 1200 N Central Ave, Glendale, CA 91202, United States

November 18, 2020 12:00 PM

“T8CCR 3203(a) - No temperature screening for employees. No social distancing. Cashiers do not wash their hands frequently and are not cleaning belts. Bathrooms are not cleaned frequently.

Alleged Hazards: 4, Employees Exposed: 25
Source: Osha.gov | Receipt Date: 2020-09-03 See Less
Reported By SafelyHQ.com User

Covid-19 OSHA Complaint, Ralphs, 10901 Ventura Blvd, Studio City, California 91604, USA

Ralphs, 10901 Ventura Blvd, Studio City, California 91604, USA

October 27, 2020 12:00 PM

“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 h... See Moreas 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
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Reported By SafelyHQ.com User

Covid-19 OSHA Complaint, Ralphs, 659 East Palomar Street, Chula Vista, California 91911, USA

Ralphs, 659 East Palomar Street, Chula Vista, California 91911, USA

September 22, 2020 12:00 PM

“T8 CCR 3203(a)(6) Employer is not enforcing social distancing. Self checkout stands are all open and the employee assigned to assist customers is within 3 ft. of the customers.

Alleged Hazards: 1, Employees Exposed: 30
Source: Osha.gov | Receipt Date: 2020-08-28 See Less
Reported By SafelyHQ.com User

Covid-19 OSHA Complaint, Ralphs, 9470 Las Tunas Dr, Temple City, California 91780, USA

Ralphs, 9470 Las Tunas Dr, Temple City, California 91780, USA

September 17, 2020 12:00 PM

“T8CCR 3203(a)(4) - COVID-19 hazard, after3pm employer stops sanitizing store touchpoints completely.

Alleged Hazards: 1, Employees Exposed: 1
Source: Osha.gov | Receipt Date: 2020-07-25 See Less
Reported By SafelyHQ.com User

Recent Interesting Reports

January 21, 2021 7:07 PM

“I saw an ad for a blackcass hand held chainsaw. What arrived was only a chain. Never received anything else See Less
Reported By SafelyHQ.com User

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
Reported By SafelyHQ.com User

January 23, 2021 6:40 PM

“Anaphylaxis is a severe, life-threatening allergic reaction. It can occur after vaccination, but is rare.

The CDC released a report on Jan 17th 2021 stating that:

During December 21, 2020–January 10, 2021, monitoring by the Vaccine Adverse Event Reporting System detected 10 cases of anaphylax... See Moreis after administration of a reported 4,041,396 first doses of Moderna COVID-19 vaccine (2.5 cases per million doses administered). In nine cases, onset occurred within 15 minutes of vaccination. No anaphylaxis-related deaths were reported.

The implications for public health practice:

Locations administering COVID-19 vaccines should adhere to CDC guidance, including screening recipients for contraindications and precautions, having necessary supplies and staff members available to manage anaphylaxis, implementing recommended post-vaccination observation periods, and immediately treating suspected anaphylaxis with intramuscular epinephrine injection.

Source: CDC.gov
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Reported By SafelyHQ.com User

December 28, 2020 8:00 PM

“Company name: Sunstar Americas, Inc.
Brand name: Paroex
Product recalled: Paroex Chlorhexidine Gluconate Oral Rinse, 4 oz and 16 oz
Reason of the recall: Potential contamination with Burkholderia lata
FDA Recall date: December 28, 2020
Recall details: Schaumburg, Illinois, Sunstar Americas, I... See Morenc. (SAI) is voluntarily recalling Paroex® Chlorhexidine Gluconate Oral Rinse USP, 0.12% products bearing an expiration date from 12/31/2020 – 9/30/2022 to the consumer level. This product may be contaminated with the bacteria Burkholderia lata. This is an expansion of the recall initially announced on October 27, 2020. Use of the defective product in the immunocompetent host may result in oral and, potentially, systemic infections requiring antibacterial therapy. In the most at-risk populations, the use of the defective product may result in life-threatening infections, such as pneumonia and bacteremia.

To date, 29 adverse events have been reported to SAI related to this recall. Affected patients tested positive for Burkholderia lata infections, typically found in sputum cultures while under treatment for other serious medical conditions. Use of the contaminated product on patients with pre-existing respiratory conditions, including those infected with Covid-19, is particularly unsafe.

The prescription oral rinse product, available through healthcare professionals only, is indicated for use as part of a professional program for the treatment of gingivitis and is packaged as follows:

- 1789P GUM® Paroex® is distributed in cases each containing 6 amber bottles of 16 fluid ounce (473 ml) chlorhexidine rinse. The bottle has a childproof cap and a 15 ml metered dosage cup, is safety sealed, and is decorated with a multiple-panel wrap-around label.
- 1788P GUM® Paroex® is distributed in cases each containing 24 amber bottles of 4 fluid ounce (118.25 ml) chlorhexidine rinse. The bottle has a childproof cap, is safety sealed, and is decorated with a multiple-panel wrap-around label.

The product can be identified as shown in the images below Paroex was distributed Nationwide to Dental offices, Dental distributors, Pharmaceutical wholesalers, Dental schools, and Pharmacies. SAI is notifying its direct distributors and customers by USPS Priority mail and is arranging for return of all recalled products. Patients, pharmacies, and healthcare facilities in possession of these products should stop using and dispensing immediately.

Consumers with questions regarding this recall can contact SAI by phone at 1-800-528-8537 or email us.pcr@us.sunstar.com on Monday-Friday from 8am-5pm CST. Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to using this drug product. Affected products and lot numbers follow below:

-Paroex® Chlorhexidine Gluconate Oral Rinse USP, 0.12% Size/ Form: 16 fl.oz. Amber Bottles. NDC #: 052376-021-02. Product Code: 1789P. Lots Recalled: ALL LOTS with expiration date from Dec. 31, 2020 through Sep. 30, 2022

- Paroex® Chlorhexidine Gluconate Oral Rinse USP, 0.12% Size/ Form: 4 fl.oz. Amber Bottles NDC #: 052376-021-04. Product Code: 1788P. Lots Recalled: ALL LOTS with expiration date from Dec. 31, 2020 through Sep. 30, 2022.

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. Complete and submit the report Online Regular Mail or Fax: Download form or call 1- 800-332-1088 to request a reporting form, then complete and return to the address on the pre-addressed form, or submit by fax to 1-800-FDA-0178. Sunstar is committed to delivering safe, fully compliant products of the highest quality and is taking necessary steps to prevent future occurrence of this issue. 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
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Reported By SafelyHQ.com User

January 14, 2021 11:44 AM

“I wonder how many people were duped by this disreputable company! Guess I should know better than to order from a company I know nothing about! Shame on them for taking hard earned money during this day and time. And shame on Facebook for allowing them to advertise. See Less
Reported By SafelyHQ.com User

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
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Reported By SafelyHQ.com User

Moderna Covid19 vaccine, New Jersey, USA

Symptoms: Fever Chills Muscle Pain Soreness
New Jersey, USA

January 25, 2021 11:34 PM

“My first Moderna injection gave me minor symptoms. The first 30 min after the injection I felt slight soreness in the injection site. As the day progressed my arm got very sore where it was hard to lift it above my shoulder. Before bed I felt muscle aches and chills. Overnight I got a 101.7 fever wh... See Moreich decreased to 100.6 a few hours later. My temp remained around 100 for several more hours before I took 2 Tylenol tablets. After I took the Tylenol my fever, aches and chills went away, but my arm remained sore for a few more days. See Less
Reported By SafelyHQ.com User

January 1, 2021 8:08 AM

“Ordered Stihl pruner from Blackcass. 2020 Hot Selling GTA 26 Battery Powered Wood Cutter $29.99. Says style Outdoor Portable Carbon Steel Chain. I assumed this meant the chain was carbon steel. Ad goes on to list what's included. You can view their ads online. Received the chain only. When I contac... See Moreted company, they informed me I had only ordered the chain. Who buys just the chain? I am finding others who are experiencing the same issue. Disputing through PayPal also. Feel this is quite the scam. See Less
Reported By SafelyHQ.com User

January 12, 2021 2:00 PM

“Company name: Midwestern Pet Foods Inc.
Brand name: Sportmix, Nunn Better, ProPac, and Others
Product recalled: Dog and Cat Pet Food
Reason of the recall: Aflatoxin Levels Exceed Acceptable Levels
FDA Recall date: January 11, 2021
Recall details: Company Announcement Midwestern Pet Foods, Inc.,... See Moreof Evansville, IN is expanding its December 30, 2020 voluntary recall of certain dog and cat food products produced in our Chickasha Operations Facility to include all dog and cat pet food products made with corn products because those products may contain aflatoxin levels which exceed acceptable limits. Products were distributed nationally to online distributors and retail stores nationwide. Midwestern Pet Foods is expanding its voluntary recall out of an abundance of caution to help protect the health and safety of pets. The products recalled cover all that expire on or before July 9, 2022, depicted as “07/09/22” in the date code on the product, as discussed below. Products with expiration dates after 07/09/22 are not included in the recall. 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 certain lots of products. No human illnesses have been reported. Out of an abundance of caution, we have expanded this recall to cover all corn products containing pet foods with expiration dates prior to 07/09/22. 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 and best buy date. Lot code information may be found on the back of bag and will appear in a three‐line code, with the top line in format “EXP 03/03/22/05/L#/B###/HH:MM”.

As explained above, this recall covers ONLY product manufactured at Midwestern Pet Food’s Chickasha, Oklahoma facility. Note that the unique Chickasha Facility identifier is located in the date code as a“05” and “REG. OK‐PFO‐0005” at the end of the date code.

In addition, the only Midwestern Pet Foods facility that produces product bearing a three‐line date code is our Chickasha Facility (See first image below).

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 food in a way that children, pets and wildlife cannot access them. Wash and sanitize pet food bowls, cups, and storage containers. Always ensure you wash and sanitize hands after handling recalled food or any utensils which have contacted recalled food. 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 voluntary recall is being conducted in cooperation with the U.S. Food and Drug Administration. All other Midwestern Pet Foods products are unaffected by this recall action. Recalled products are as follows, with lot codes found in Expanded Recall Lot Numbers:

Pro Pac Adult Mini Chunk
Pro Pac Performance Puppy
Splash Fat Cat 32%
Nunn Better Maintenance
Sportstrail 50
Sportmix Original Cat 15
Sportmix Original Cat 31
Sportmix Maintenance 44
Sportmix Maintenance 50
Sportmix High Protein 50
Sportmix Energy Plus 44
Sportmix Energy Plus 50
Sportmix Stamina 44
Sportmix Stamina 50
Sportmix Bite Size 40
Sportmix Bite Size 44
Sportmix High Energy 44
Sportmix High Energy 50
Sportmix Premium Puppy 16.5
Sportmix Premium Puppy 33

Check the full recall details on fda.gov

Source: FDA
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Reported By SafelyHQ.com User

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
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Reported By SafelyHQ.com User