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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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Porterville, California, United States

Updated: January 14, 2021 12:00 PM

Covid-19 OSHA Complaint, Sun Pacific, 23744 Avenue 181, PORTERVILLE, CA, 93257, USA

Sun Pacific, 23744 Avenue 181, PORTERVILLE, CA, 93257, USA

January 14, 2021 12:00 PM

“Not enforcing the COVID-19 rules of testing employees.


Source: Osha.gov | Receipt Date: 2020-11-20 See Less
Reported By SafelyHQ.com User

Covid-19 OSHA Complaint, Sequoia Family Health Center, 590 West Putnam Ave., PORTERVILLE, CA, 93257, USA

Sequoia Family Health Center, 590 West Putnam Ave., PORTERVILLE, CA, 93257, USA

January 14, 2021 12:00 PM

“T8 CCR 5199 On 6/20/2020 attending physician did not show up for work. When asked where the physician was another employee made a gesture to be quiet. Was told by office staff had some kind of stomach bug. On 6/24/2020 office manager announced that the physician had tested positive for COVID-19. Sev... See Moreeral office staff was present during the announcement. Thinks physician may have taken a COVID test 6/20/2020 or 6/21/2020. May have exposed the office staff as well as patients. Hazard Location: 590 West Putnam Ave., Porterville, CA 93257 Notes: Complainant stated the clinic tested the employees for the virus, however were not given the results. Tests were administered by someone not qualified to give them. Complainant had his own test done and tested positive. Complainant became sick and was off work for three weeks. He was only paid for two weeks of workman's comp. Complainant states that three other employees also tested positive as well as other employees in different medical suites. Stated that the physician treated patients even though he tested positive and that they had a pot luck gathering even though he tested positive. States that the clinic was not cleaned or sanitized.


Source: Osha.gov | Receipt Date: 2020-09-29
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Reported By SafelyHQ.com User

Covid-19 OSHA Complaint, All Creatures Pet Care Center, 842 North Westwood Street, PORTERVILLE, CA, 93257, USA

All Creatures Pet Care Center, 842 North Westwood Street, PORTERVILLE, CA, 93257, USA

December 30, 2020 12:00 PM

“1. Social distancing not enforced. 2. Employer failed quarantine employees that tested positive for COVID-19


Source: Osha.gov | Receipt Date: 2020-11-16 See Less
Reported By SafelyHQ.com User

Covid-19 OSHA Complaint, Home Depot, 750 S Jaye St, PORTERVILLE, CA, 93257, USA

Home Depot, 750 S Jaye St, PORTERVILLE, CA, 93257, USA

December 5, 2020 12:00 PM

“3203(a)4 Employer not notifying employees of COVID 19 positive co-workers. Not practicing social distancing while in break room and no hand sanitizer.


Source: Osha.gov | Receipt Date: 2020-11-09 See Less
Reported By SafelyHQ.com User

Covid-19 OSHA Complaint, Home Depot, 750 S Jaye St, PORTERVILLE, CA, 93257, USA

Home Depot, 750 S Jaye St, PORTERVILLE, CA, 93257, USA

December 5, 2020 12:00 PM

“3203(a)4 Employer not notifying employees of COVID 19 positive co-workers. Not practicing social distancing while in break room and no hand sanitizer.


Source: Osha.gov | Receipt Date: 2020-11-09 See Less
Reported By SafelyHQ.com User

Covid-19 OSHA Complaint, Greg's Xpress Oil Change, Olive Avenue, Porterville, CA 93257, USA

Greg's Xpress Oil Change, Olive Avenue, Porterville, CA 93257, USA

November 25, 2020 12:00 PM

“Employer not following COVID-19 recommendation.

Alleged Hazards: 1, Employees Exposed: 5
Source: Osha.gov | Receipt Date: 2020-10-30 See Less
Reported By SafelyHQ.com User

Covid-19 OSHA Complaint, Tulare County, Office of the District Attorney, 16 E Olive Ave, Porterville, CA 93257, USA

Tulare County, Office of the District Attorney, 16 E Olive Ave, Porterville, CA 93257, USA

November 10, 2020 12:00 PM

“3203(a)(4) Employees who have been exposed to COVID-19 still came to work and court, exposing more people.

Alleged Hazards: 1, Employees Exposed: 40
Source: Osha.gov | Receipt Date: 2020-10-20 See Less
Reported By SafelyHQ.com User

Covid-19 OSHA Complaint, DeBoer Homes Inc, 2211 W Orange Ave, Porterville, CA 93257, USA

DeBoer Homes Inc, 2211 W Orange Ave, Porterville, CA 93257, USA

November 10, 2020 12:00 PM

“1. Employee works at a home for residential treatment facility with clients and was terminated for expressing worries of being exposed to the corona virus. Employee was off work for 2-3 weeks after they had a fever of 101.2 degrees. Employee are provide with PPE when around clients.


Source: Os... See Moreha.gov | Receipt Date: 2020-09-21 See Less
Reported By SafelyHQ.com User

Covid-19 OSHA Complaint, Walmart, 1250 W Henderson Ave, Porterville, California 93257, USA

Walmart, 1250 W Henderson Ave, Porterville, California 93257, USA

October 22, 2020 12:00 PM

“1. Complainant states that employer is not enforcing Covid-19 policies and procedures, when in breakroom no masks, no social distancing and no sanitizer. Breakroom cleaned twice during the day. No mask or social distancing while in the back of store. Associates that may have exposed to the virus... See Moreare not wearing masks and following protocol are showing up for work. Employees who show symptoms must go to the store to be tested. Store is only requiring 10 day quarantine.

Alleged Hazards: 1, Employees Exposed: 1
Source: Osha.gov | Receipt Date: 2020-09-24
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Reported By SafelyHQ.com User

Covid-19 OSHA Complaint, Holiday Inn Express & Suites Porterville, 840 S Jaye St, Porterville, California 93257, USA

Holiday Inn Express & Suites Porterville, 840 S Jaye St, Porterville, California 93257, USA

August 20, 2020 12:00 PM

“3203(a)(4) The employer is not ensuring sanitation practices are being performed. Housekeeping is working with very limited PPE. The employer is telling housekeeping staff they are to use only three pairs of gloves per day. Employees clean toilets, microwaves and coffee pots with the same pair of gl... See Moreoves in several rooms, without allowing a glove change. The employer may have failed to evaluate the hazard of not following CDC guidelines amidst the COVID-19 pandemic; those guidelines are outlined on the dir.ca.gov and www.osha.gov websites.

Alleged Hazards: 1, Employees Exposed: 1
Source: Osha.gov | Receipt Date: 2020-05-07
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Reported By SafelyHQ.com User

Recent Interesting Reports

December 23, 2020 10:00 PM

“Company name: Shane Erickson, Inc. DBA Innovative Marketing Consultants
Brand name: IMC
Product recalled: Wash-Free Hand Sanitizer
Reason of the recall: Undeclared Methanol
FDA Recall date: December 23, 2020
Recall details: Shane Erickson, Inc. is voluntarily recalling lot 2020/05/11 and MFG:... See More2020/05/10 L/N: 20200510-3 of imc Wash-Free Hand Sanitizer 50 ml, 100 ml, 300 ml and Wash Free Hand Sanitizer 300 ml lot 2020/05/11 and Thrifty White Pharmacy Wash-Free Hand Sanitizer 300 ml lot 2020/05/11 listed in the table below to the consumer level. The products are being recalled due to the potential presence of methanol (wood alcohol).

Risk Statement: 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 accidentally 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, Shane Erickson, Inc. has not received any reports of adverse events related to the product(s) of this recall. Recalled Products:

- IMC Wash-Free Hand Sanitizer 50 ml, 1.7 oz (8 19845 00597 8). Lot: 43962. Expiration date: 45056
- IMC Wash-Free Hand Sanitizer 100 ml, 3.4 oz (8 19845 00598 5). Lot: MFG: 2020/05/10 L/N: 20200510-3. Expiration date: N/A
- IMC Wash-Free Hand Sanitizer | Wash-Free Hand Sanitizer | Thrifty White Pharmacy Wash-Free Hand Sanitizer 300 ml, 10.14 oz (8 19845 00599 2). Lot: 43962. Expiration date: 45056

The product is used as a hand sanitizer for handwashing to decrease bacteria on the skin when soap and water are not available. All products are packaged in a plastic bottle. The 50 ml are in a HDPE opaque white bottle with a blue cap, the 100 ml is in a clear PET bottle with a clear cap and the 300 ml are in a clear PET bottle with a black pump. The product can be identified by checking the product size, UPC details, lot number and expiration date on the bottle containing the product. The product can also be identified by this information on the back label: Made in China, Distributed by IMC 4284 Shoreline Dr, Spring Park, MN 55384, YUEWEIXIAOZHENGZI (2020) - 04 - No. 0023.

Some of the product has custom front labels (see examples below) the back label on the custom labels have the same identification information as previously mentioned above. The hand sanitizer was distributed Nationwide in the USA to wholesale and retail customers.

Shane Erickson, Inc. is notifying its distributors and customers by mail/email and is arranging for the return of all recalled products. Consumer, distributors, and retailers that have product, which is being recalled, should stop use or distribution and return to place of purchase. Consumers with questions regarding this recall can contact Shane Erickson, Inc. by phone at 952.252.1254 [Call: 952.252.1254] or email sales@imcsuccess.com Monday through Friday from 8:00 am to 5:00 pm Central Time Zone.

Check the full recall details on fda.gov

Source: FDA
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Reported By SafelyHQ.com User

January 14, 2021 8:47 PM

“The owner refused to wipe down the countertop or the card swipe after me requesting him to do so after several people using it. I want everyone to refrain from going to this station since he does nothing to protect people during covid 19 See Less
Reported By SafelyHQ.com User

January 14, 2021 10:51 PM

“Same thing happened to me ordered this product got the chain had to go back and purchase the saw. It says it a Stihl in a nice case and it come in a box unknown name. False fake advertising from start to finish. Playing games on getting answers from them on why this is not the product I ordered. 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

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 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 8, 2021 6:01 PM

“Company name: Fresenius Kabi USA
Brand name: Fresenius Kabi
Product recalled: Ketorolac Tromethamine Injection, USP, 30 mg/mL
Reason of the recall: Presence of particulate matter
FDA Recall date: January 08, 2021
Recall details: Fresenius Kabi USA is voluntarily recalling a single lot of Ketoro... See Morelac Tromethamine Injection, USP, 30 mg/mL, 1 mL fill in a 2 mL amber vial to the user level due to the presence of particulate matter. Particulate matter was found in reserve sample vials. No adverse event reports have been received for the recalled lot, which was produced and sold in 2019.

Administration of products containing particulate matter could obstruct blood vessels and result in local irritation of blood vessels, swelling at the site of injection, a mass of tissue that could become inflamed and infected, blood clots traveling to the lung, scarring of the lung tissues, and allergic reactions that could lead to life-threatening consequences.

Ketorolac Tromethamine, a nonsteroidal anti-inflammatory drug, is indicated for the short-term (up to 5 days in adults) management of moderately severe acute pain that requires analgesia at the opioid level. The total combined duration of use of oral Ketorolac Tromethamine and Ketorolac Tromethamine Injection should not exceed 5 days. Listed below is a table of the recalled lot distributed nationwide in the United States to wholesalers, distributors, hospitals, and pharmacies between March 28, 2019 and September 3, 2019.

Product Name/Product size: Ketorolac Tromethamine Injection, USP, 30mg / mL, 1 mL fill in a 2 mL amber vial
NDC Number: 63323-162-01
Product Code: 160201
Batch Number: 6121083
Expiration Date: 02/2021
First Ship Date: 03/28/2019
Last Ship Date: 09/03/2019

Fresenius Kabi is notifying its distributors and customers by letter and asking customers and distributors to check their stock immediately and to quarantine and discontinue the use and distribution of any affected product. Distributors should notify their customers and direct them to quarantine and discontinue distributing or dispensing the affected lot, and to return the product to Fresenius Kabi.

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 5, 2021 9:18 AM

“On 12/6/20, I had ordered 2 chainsaws as Christmas gifts for $65.97, but only received 2 vinyl pouches containing the chains to the saws. I contacted the seller to find out when I could expect the delivery on the saws, along with any tracking info they could provide on the items. A few days later th... See Moreey contacted me by email saying for me to check my order details, what I had ordered was the chains, and if I wanted the saws they were $89.99 each. So since I paid through PayPal, I will be reporting the issue and trying to retrieve my monies back. See Less
Reported By SafelyHQ.com User

January 4, 2021 10:32 PM

“Totally false advertising. I order two chainsaws and got two open 26" chains with straps on both ends. Not happy. This advertising was misleading and took over 30 days to receive this product in the mail. I am totally dissatisfied with this purchase and company. See Less
Reported By SafelyHQ.com User