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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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Restaurant

Updated: January 15, 2021 5:16 PM

Northern Lights Pizza - No masks, Northern Lights Pizza, Southwest 9th Street, Des Moines, IA, USA

Northern Lights Pizza, Southwest 9th Street, Des Moines, IA, USA

January 15, 2021 5:16 PM

“Customer here. Walked in to pick up my pizza NONE of the employees including the owner had a mask on. Working in close proximity as well. See Less
Reported By Iwaspoisoned.com User

MASKLESS CASHIER DRIVE THRU WINDOW, Dairy Queen (Treat), E Queen Creek Rd, Gilbert, AZ 85297, United States

Dairy Queen (Treat), E Queen Creek Rd, Gilbert, AZ 85297, United States

January 15, 2021 4:33 PM

“The middle aged woman cashier in the drive thru window on Friday, January 15, 2021 at around 2:15pm was maskless. This is not acceptable. She was exposing everyone in the drive thru because she wasn’t wearing a mask. She was handling both food and money. See Less
Reported By Iwaspoisoned.com User

Covid-19 OSHA Complaint, BURGERVILLE LLC, 818 Harrison Ave, CENTRALIA, WA, 98531, USA

BURGERVILLE LLC, 818 Harrison Ave, CENTRALIA, WA, 98531, USA

January 14, 2021 12:00 PM

“A sick employee continued to work until testing Covid-19 positive. Coworkers informed Management of the sick employee, Management did nothing to rectify the situation. Management did not inform employees that their coworker was Covid-19 positive. Social distancing measures are not taken seriously. B... See Moreurgerville 818 Harrison Ave Centralia, Wa 98531


Source: Osha.gov | Receipt Date: 2020-12-01
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Reported By Iwaspoisoned.com User

Covid-19 OSHA Complaint, PAN WASHINGTON LLC, 915 Se 164th Ave, VANCOUVER, WA, 98683, USA

PAN WASHINGTON LLC, 915 Se 164th Ave, VANCOUVER, WA, 98683, USA

January 14, 2021 12:00 PM

“All employees and guests are at risk of contracting COVID-19 as the business is not enforcing face coverings, not blocking off tables that are not socially distanced, and allowing more than 25% of capacity.


Source: Osha.gov | Receipt Date: 2020-07-23 See Less
Reported By Iwaspoisoned.com User

Covid-19 OSHA Complaint, L & S RESTAURANTS INC, 626 S Hill Park Dr, PUYALLUP, WA, 98373, USA

L & S RESTAURANTS INC, 626 S Hill Park Dr, PUYALLUP, WA, 98373, USA

January 14, 2021 12:00 PM

“Alleged Hazards: - One employee tested positive for COVID-19 and the employer has not informed other employees they may have been exposed. - The employer is not disinfecting the restaurant after finding out about the positive case


Source: Osha.gov | Receipt Date: 2020-11-05 See Less
Reported By Iwaspoisoned.com User

Covid-19 OSHA Complaint, Reiner Inc, 1032 Nw Galveston Ave, BEND, OR, 97701, USA

Reiner Inc, 1032 Nw Galveston Ave, BEND, OR, 97701, USA

January 14, 2021 12:00 PM

“Serious

Alleged Hazards: 1,
Source: Osha.gov | Receipt Date: 2020-11-12 See Less
Reported By Iwaspoisoned.com User

Covid-19 OSHA Complaint, Dancing Beans Coffee LLC, 225 SE 5th St, MADRAS, OR, 97741, USA

Dancing Beans Coffee LLC, 225 SE 5th St, MADRAS, OR, 97741, USA

January 14, 2021 12:00 PM

“Serious

Alleged Hazards: 1,
Source: Osha.gov | Receipt Date: 2020-10-24 See Less
Reported By Iwaspoisoned.com User

Covid-19 OSHA Complaint, Pinocchio's Pizza Inc, 1795 E Main St, COTTAGE GROVE, OR, 97424, USA

Pinocchio's Pizza Inc, 1795 E Main St, COTTAGE GROVE, OR, 97424, USA

January 14, 2021 12:00 PM

“Serious

Alleged Hazards: 1,
Source: Osha.gov | Receipt Date: 2020-10-13 See Less
Reported By Iwaspoisoned.com User

Covid-19 OSHA Complaint, Pieology Pizzeria, Springfield, Springfield, OR 97477, United States

Pieology Pizzeria, Springfield, Springfield, OR 97477, United States

January 14, 2021 12:00 PM

“Serious

Alleged Hazards: 1,
Source: Osha.gov | Receipt Date: 2020-08-10 See Less
Reported By Iwaspoisoned.com User

Covid-19 OSHA Complaint, Papa John's Pizza, 6372 SW Capitol Hwy, Portland, OR 97201, USA

Papa John's Pizza, 6372 SW Capitol Hwy, Portland, OR 97201, USA

January 14, 2021 12:00 PM

“Serious

Alleged Hazards: 2,
Source: Osha.gov | Receipt Date: 2020-12-01 See Less
Reported By Iwaspoisoned.com User

Recent Interesting Reports

January 7, 2021 1:49 PM

“BlackCass. I ordered a hand-held saw and received only an extra chain. Can I get a refund? See Less
Reported By SafelyHQ.com User

January 14, 2021 8:51 PM

“I am a teacher and am authorized to get the Moderna vaccine. I made an appointment in Ridgewood 2 days ago. Appoint was at 5:20 but didn't get my shot until 7:40. The lines are extremely long at night. But the nurse said they are empty in the morning. Once you get inside it is very fast, everyone is... See Morevery helpful and you can sign up for your second vaccine. They make you wait 15 mins to make sure you're ok before you leave. I have no side effects from the shot and feel fine. See Less
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 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 1, 2021 9:01 PM

“Company name: Precision Dose Inc.
Brand name: GUM Paroex
Product recalled: Paroex Chlorhexidine Gluconate Oral Rinse, 15 mL unit dose cups
Reason of the recall: Potential contamination with Burkholderia lata
FDA Recall date: December 31, 2020
Recall details: Company Announcement Precision Dose,... See MoreInc. is voluntarily recalling all lots of Chlorhexidine Gluconate Oral Rinse USP, 0.12%, 15mL Unit Dose Cups bearing an expiration date from 1/31/2021 – 02/28/2022 (see specific lots below) to the consumer level. Precision Dose, Inc. was notified by the manufacturer of the product, Sunstar Americas, Inc., that this product may be contaminated with the bacteria Burkholderia lata.

From information provided by the manufacturer, Sunstar Americas, Inc., 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 pneumonia and bacteremia.

To date, no adverse events have been reported to Precision Dose, Inc. related to this recall. 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 the product impacted is:

- Distributed in cases each containing 3 shrink-wrapped plastic trays each with 10 unit dose cups, 30-pack. NDC 68094-028-62
- Distributed in cases each containing 10 shrink-wrapped plastic trays each with 10 unit dose cups, 100-pack. NDC 68094-028-61

Chlorhexidine Gluconate Oral Rinse was distributed nationwide in the USA to pharmaceutical wholesalers. Precision Dose, Inc. is notifying its consignees directly and is arranging for return of all recalled product. Patients, pharmacies, and healthcare facilities in possession of these products should stop using and dispensing immediately.

Consumers with questions regarding this recall can contact Precision Dose, Inc. at 1 (800) 397-9228 (Monday-Friday, 8:00 AM to 4:30 PM Central Time) or by email to customercare@precisiondose.com. Consumers should contact their physician or healthcare provider if they have experienced problems that may be related to using this drug product. Affected products and lot numbers follow below: AFFECTED LOTS-Chlorhexidine Gluconate Oral Rinse USP, 0.12%

Check the full recall details on fda.gov

Source: FDA
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Reported By SafelyHQ.com User

January 8, 2021 12:49 PM

“On December 14, 2020 I ordered the Blackcass battery operated chainsaw. On January 8, 2021 I received a chain with two handles attached. See Less
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 13, 2021 4:58 PM

“Yes my little Angie was given a dream bone on Sept 26, 2020 at 7:30 pm at 8:pm she threw up the dream bone and then a few times with fluid and then collapsed on the floor her jaw was tight. I grabbed her up and rushed her to the vet. She had been poisoned by the dream bones her favourite treat. S... See Morehe started hemorraging blood out her butt, after transfusion it stopped around 4.30 am sept 27th then they called me to say her heart stopped and they revived her and she was on a ventolator and when I got there awww so sad poor thing. She was now bleeding in her lungs OH MY GOD. She passed away that morning. I cried for 2 and a half hours in the room with her dead I just could not bear to leave her. The vet bill was over 2400 dollars and she was gone in 12 hours after eating that stupid dream bone. I still have the package of treats. I bought them at Walmart. She was not even 2 years old yet. See Less
Reported By SafelyHQ.com User

December 30, 2020 9:21 AM

“The FDA is alerting pet owners and veterinary professionals about certain Sportmix pet food products manufactured by Midwestern Pet Foods, Inc. that may contain potentially fatal levels of aflatoxin. As of December 30, 2020, 28 deaths and 8 illnesses in dogs that ate the recalled product have been r... See Moreeported. This is an ongoing investigation. Case counts and the scope of this recall may expand as new information becomes available.

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. Pets experiencing aflatoxin poisoning may have symptoms such as sluggishness, loss of appetite, vomiting, jaundice (yellowish tint to the eyes or gums due to liver damage), and/or diarrhea. In severe cases, this toxicity can be fatal. In some cases, pets may suffer liver damage but not show any symptoms.

Pet owners should stop feeding their pets the recalled products listed below and consult their veterinarian, especially if the pet is showing signs of illness. The pet owner should remove the food and make sure no other animals have access to the recalled product. Sanitize pet food bowls, scoops, and storage containers using bleach, rinsing well afterwards with water, and drying thoroughly. There is no evidence to suggest that pet owners who handle products containing aflatoxin are at risk of aflatoxin poisoning.

Midwest Pet Food, Inc. already recalled the following lots of Sportmix pet food products:
- Sportmix Energy Plus, 50 lb. bag. Lots: Exp 03/02/22/05/L2 | Exp 03/02/22/05/L3 | Exp 03/03/22/05/L2
- Sportmix Energy Plus, 44 lb. bag. Lot: Exp 03/02/22/05/L3
- Sportmix Premium High Energy, 50 lb. bag. Lot: Exp 03/03/22/05/L3
- Sportmix Premium High Energy, 44 lb. bag. Lot: Exp 03/03/22/05/L3
- Sportmix Original Cat, 31 lb. bag. Lot: Exp 03/03/22/05/L3
- Sportmix Original Cat, 15 lb. bag. Lots: Exp 03/03/22/05/L2 | Exp 03/03/22/05/L3

Check the full outbreak announcement on fda.gov

Source: FDA
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Reported By SafelyHQ.com User

January 4, 2021 11:39 PM

“I ordered this saw on December 13th, on December 15th I recieved a confirmation notice the my purchase was on its way, today January 4th 2021 in the mail all I recieved was a chain. Is this a scam or what,and where is the rest of my purchased SAW????? See Less
Reported By SafelyHQ.com User