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Simi Valley, California, United States

Updated: December 30, 2020 12:00 PM

Covid-19 OSHA Complaint, Simi Valley Unified School District / Santa Susana Elmentary School, 4300 Apricot Lane, SIMI VALLEY, CA, 93065, USA

Simi Valley Unified School District / Santa Susana Elmentary School, 4300 Apricot Lane, SIMI VALLEY, CA, 93065, USA

December 30, 2020 12:00 PM

“California Code of Regulations, Title 8, Section 3203(a)(4) and (6). Injury and Illness Prevention Program. The Employer is not taking measures to protect employees from exposure to the COVID-19 virus, as follows: - The Employer is not enforcing the use of protective masks in office areas. For insta... See Morence, the Employer is permitting employees to remove their face coverings while they are working indoors as long as their desks are positioned 6-feet apart. In addition, employees do not consistently wear face coverings indoors while using shared office equipment. - Restrooms, other common areas and shared office equipment are not effectively disinfected. - The Employer does not provide employees with disinfectants to clean their office areas. Complainant notes: -The ER ensures strict adherence to COVID-19 precautions in the District HR office, however adherence to the precautions and resources provided to protect employees form the COVID-19 virus are much more less in the elementary schools. -The Custodian does not clean anything. EE took photos after summer breaks. The door knobs were covered with spider Complainant will be working from home, but she is concerned for the health of EEs and spreading the virus in the community.

Alleged Hazards: 1,
Source: Osha.gov | Receipt Date: 2020-08-18
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Reported By SafelyHQ.com User

Covid-19 OSHA Complaint, Simi Valley Unified School District / Justin Elementary School, 2245 North Justin Ave., SIMI VALLEY, CA, 93065, USA

Simi Valley Unified School District / Justin Elementary School, 2245 North Justin Ave., SIMI VALLEY, CA, 93065, USA

December 30, 2020 12:00 PM

“California Code of Regulations, Title 8, Section 3203(a)(4) and (6). Injury and Illness Prevention Program. The Employer is not taking measures to protect employees from exposure to the COVID-19 virus, as follows: - The Employer is not enforcing the use of protective masks in office areas. For insta... See Morence, the Employer is permitting employees to remove their face coverings while they are working indoors as long as their desks are positioned 6-feet apart. In addition, employees do not consistently wear face coverings indoors while using shared office equipment. - Restrooms, other common areas and shared office equipment are not effectively disinfected. - The Employer does not provide employees with disinfectants to clean their office areas. Complainant notes: -The ER ensures strict adherence to COVID-19 precautions in the District HR office, however adherence to the precautions and resources provided to protect employees form the COVID-19 virus are much more less in the elementary schools. -The Custodian does not clean anything. EE took photos after summer breaks. The door knobs were covered with spider Complainant will be working from home, but she is concerned for the health of EEs and spreading the virus in the community.

Alleged Hazards: 1,
Source: Osha.gov | Receipt Date: 2020-08-18
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Reported By SafelyHQ.com User

Covid-19 OSHA Complaint, Eureka Productions, 2940 Kuehner Dr., SIMI VALLEY, CA, 93063, USA

Eureka Productions, 2940 Kuehner Dr., SIMI VALLEY, CA, 93063, USA

December 30, 2020 12:00 PM

“"Over 120 employees in our crew, including Hosts and Casts. White Page protocol not being followed regularly. Production team and production company employees do not wear masks while inside at their open-air office desks and more often than do not observe social distancing protocol when interacting.... See MoreThe production Manager in charge of COVID protocol is a regular offender of these violations as well, leaving us a lack of confidence in our safety. Our COVID safety office was fired on Wednesday for being "too aggressive" in his enforcement of Policy. (i.e.: asking people to separate to 6', wear their mask properly, etc.). Since his departure, masks enforcement is considerably more lax, scheduled temperature checks have gone missed, and production was witnessed approaching and hugging another employee just this morning. Pods are consistently cross-contaminated by crew members, exposing our cast to Zone B Crew members." EE do not wear masks Not social distancing

Alleged Hazards: 1,
Source: Osha.gov | Receipt Date: 2020-08-07
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Reported By SafelyHQ.com User

Covid-19 OSHA Complaint, Burns Environmental, 855 East Easy Street, Simi Valley, CA 93065, USA

Burns Environmental, 855 East Easy Street, Simi Valley, CA 93065, USA

December 15, 2020 12:00 PM

“At various job sites. There are about 40 EEs. 2 EEs have tested positive for COVID-19. ER is not informing in a timely manner to the EEs about the positive cases in the place of work. Complainant contracted COVID-19. He stop going to work and complainant is concern that he might have infected his co... See More-workers. Complainant informed his ER and the ER is not doing anything to prevent the spread of the virus to the other EEs.

Alleged Hazards: 1,
Source: Osha.gov | Receipt Date: 2020-07-31
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Reported By SafelyHQ.com User

Covid-19 OSHA Complaint, Meggitt Inc., 1955 Surveyor Ave., SIMI VALLEY, CA, 93063, USA

Meggitt Inc., 1955 Surveyor Ave., SIMI VALLEY, CA, 93063, USA

December 5, 2020 12:00 PM

“Employer is not adhering to CDC guidelines for the prevention of COVID-19 infection. ER is not informing and testing the other employees that have been in closed contact with COVID-19 positive employees.

Alleged Hazards: 1, Employees Exposed: 1
Source: Osha.gov | Receipt Date: 2020-08-07 See Less
Reported By SafelyHQ.com User

Covid-19 OSHA Complaint, World of Wellness, 2955 Cochran St., Unit B1, SIMI VALLEY, CA, 93065, USA

World of Wellness, 2955 Cochran St., Unit B1, SIMI VALLEY, CA, 93065, USA

December 5, 2020 12:00 PM

“1. The Employer is not taking measures to protect employees from exposure to the COVID-19 virus, as follows: - The ER is not enforcing social distancing between employees and clients. The massage services provided to clients for non medical purposes. - The ER did not notify the employees when a doct... See Moreor who works at the facility tested positive for the COVID-19 virus. - The ER did not disinfect the facility.

Alleged Hazards: 1, Employees Exposed: 1
Source: Osha.gov | Receipt Date: 2020-07-17
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Reported By SafelyHQ.com User

Covid-19 OSHA Complaint, Computer Metal Products Inc, 370 E Easy St, Simi Valley, CA 93065, USA

Computer Metal Products Inc, 370 E Easy St, Simi Valley, CA 93065, USA

November 25, 2020 12:00 PM

“CCR, T8, Section 3203(a)(4) & (a)(6) Social distancing is not maintained. CCR, Ti8, Section 3364(a) There are only 2 bathrooms for 80 plus people. CCR, T8, Section 3380(f) and 3364(d) Employees are not provided with gloves masks and hand soap.

Alleged Hazards: 3, Employees Exposed: 1
Source: O... See Moresha.gov | Receipt Date: 2020-08-31 See Less
Reported By SafelyHQ.com User

Covid-19 OSHA Complaint, Park Animal Hospital, 2767 Tapo St, Simi Valley, CA 93063, USA

Park Animal Hospital, 2767 Tapo St, Simi Valley, CA 93063, USA

November 25, 2020 12:00 PM

“The employer is not letting the patients know or customers know that the hospital had employees who tested positive for COVID-19. The employer is not enforcing the face mask policy for employees and patients or taking temperatures of the employees or patients entering the hospital.

Alleged Hazard... See Mores: 1, Employees Exposed: 1
Source: Osha.gov | Receipt Date: 2020-07-02
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Reported By SafelyHQ.com User

Dead caterpillar in my food, Costco Wholesale, Park Center Drive, Simi Valley, CA, USA

Costco Wholesale, Park Center Drive, Simi Valley, CA, USA

June 18, 2020 7:54 PM

“My 17yr old daughter was eating the Okami organic Edamame from there we bought her yesterday. She open the pod and found the pink looking Caterpillar coming out. It was dead. See Less
Reported By SafelyHQ.com User

Recent Interesting Reports

January 7, 2021 1:49 PM

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January 4, 2021 7:46 PM

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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

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 4, 2021 11:00 AM

“Company name: Essaar Inc.
Brand name: Soho Fresh
Product recalled: 70% Rubbing Alcohol
Reason of the recall: Contaminated with Methanol
FDA Recall date: January 04, 2021
Recall details: Company Announcement Essaar Inc. is voluntarily recalling lot 200528303 of Soho Fresh 70% Rubbing Alcohol... See Morein 33.81 oz. clear plastic bottles to the consumer level. FDA analysis of the product revealed it is contaminated with methanol. Substantial methanol exposure can result in nausea, vomiting, headache, blurred vision, permanent blindness, seizures, coma, permanent damage to the nervous system or death. Although all persons using these products on their hands are at risk, young children who accidently ingest these products and adolescents and adults who drink these products as an alcohol (ethanol) substitute, are most at risk for methanol poisoning.

To date, Essar Inc. has not received any reports of adverse events related to this recall. The product is used as an external purpose use rubbing alcohol and is packaged in 33.81 oz. clear plastic bottles with lot number 200528303 and UPC 7502268987367.

Soho Fresh was distributed nationwide to retail stores. Essaar Inc. is notifying its distributors and customers by email and mail and is arranging for the return of all recalled product to Essaar Inc. Consumers that have product which is being recalled should stop using and discard or return to place of purchase or to Essaar Inc. contacting via email or phone or mailing address mentioned above for arrangements of return. Consumers who have purchased this product should not open the package or use the contents. Instead, they should return the product to the location of purchase for a full refund or call Essaar Inc. at 201-647-7606 Monday to Friday 9am to 5pm, Eastern Standard Time. Essaar Inc. can also be reached via email at essaarinc@yahoo.com.

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. 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
This recall is being conducted with the knowledge of the U.S. Food and Drug Administration. FDA’s update  

Check the full recall details on fda.gov

Source: FDA
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Reported By SafelyHQ.com User

January 16, 2021 3:36 PM

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January 1, 2021 8:08 AM

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December 29, 2020 1:59 PM

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