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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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Product: Pizza

Updated: July 12, 2020 12:00 PM

July 12, 2020 12:00 PM

“Multiple employees at White House Pizza in Garfield County have tested positive for Covid-19. The restaurant is part of an active outbreak of at least 95 people.

Source: coloradoan.com See Less
Reported By SafelyHQ.com User

Employee test positive for Covid-19, Buffalo Pizza & Ice Cream Co, 2600 21st St, Sacramento, CA 95818, USA

Buffalo Pizza & Ice Cream Co, 2600 21st St, Sacramento, CA 95818, USA

July 12, 2020 12:00 PM

“An employee at Buffalo Pizza & ... See Moretitle="Product: Ice Cream">Ice Cream Co. at 2600 21st St. in Sacramento tested positive for COVID-19 on July 9.


Source: sacbee.com See Less
Reported By SafelyHQ.com User

July 8, 2020 12:00 PM

“An employee from Caliente Pizza’s Mt. Lebanon location has tested positive for Coronavirus. It is unknown when the employee worked last, but If you visited the restaurant recently, please report it and a ... See Moreny other location that you visited.


Source: pittsburgh.cbslocal.com
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Reported By SafelyHQ.com User

July 9, 2020 11:32 AM

“I’ve never been served a raw pizza like I was served a raw chicken sandwich See Less
Reported By SafelyHQ.com User

July 6, 2020 12:00 PM

“An employee at Buddy's Pizza in Portage tests positive for COVID-19 on July 3.

Source: cw7michigan.com See Less
Reported By SafelyHQ.com User

Employee test positive for Covid-19, Aldo’s Pizza Pies - Downtown, 100 S Main St, Memphis, TN 38103, USA

Aldo’s Pizza Pies - Downtown, 100 S Main St, Memphis, TN 38103, USA

July 6, 2020 12:00 PM

“A Packed House Productions (PHP) employee that visited the following restaurants - Aldo’s Pizza Pies, Bardog Tavern, Slider Inn and Momma’s - has tested positive for COVID-19. All restaurants are temporar ... See Moreily closed.

Source: wreg.com
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Reported By SafelyHQ.com User

Employee test positive for Covid-19, Firo Fire Kissed Pizza, 3902 Northwest Cache Road, Lawton, OK, USA

Firo Fire Kissed Pizza, 3902 Northwest Cache Road, Lawton, OK, USA

July 6, 2020 12:00 PM

“An employee at Firo Fire Kissed Pizza located at 3902 Cache Road in Lawton tested positive for the coronavirus.

Source: swoknews.com See Less
Reported By SafelyHQ.com User

Employee test positive for Covid-19, Grotto Pizza, Wyoming Valley Mall, Wilkes-Barre Township, PA 18702, United States

Grotto Pizza, Wyoming Valley Mall, Wilkes-Barre Township, PA 18702, United States

July 2, 2020 12:00 PM

“A wait staff member at Grotto Pizza in Wilkes-Barre Township tested positive for COVID-19.

Source: timesleader.com See Less
Reported By SafelyHQ.com User

July 2, 2020 12:00 PM

“Two wait staff members at Grotto Pizza in Harveys Lake tested positive for COVID-19.

Source: timesleader.com See Less
Reported By SafelyHQ.com User

July 1, 2020 12:00 PM

“An employee at Northwest Pizza Company in Hayden tests positive for coronavirus

Source: krem.com See Less
Reported By SafelyHQ.com User

Recent Interesting Reports

May 26, 2020 9:34 PM

“Wifey wants to thank you for the raw chicken sandwich and upcoming bout of diarrhea. PukeCity See Less
Reported By SafelyHQ.com User

July 8, 2020 4:00 PM

“Company name: CME America
Brand name: BodyGuard
Product recalled: Infusion System Administration Set (infusion set)
Reason of the recall: Use of the pump system potentially could cause over-infusion or under-infusion of therapy
FDA Recall date: July 08, 2020
Recall details: PRNewswire/ - CME Am ... See Moreerica, a wholly owned subsidiary of BD (Becton, Dickinson and Company), announced a voluntary recall for all CME America BodyGuard® Infusion System Administration Sets (infusion sets) used with the company's BodyGuard® infusion pumps—that were distributed beginning May 2016 (see complete impacted product list below).  This action was initiated on June 16, 2020. As part of CME America's commitment to quality, following the previously announced recall (April 27, 2020) of the BodyGuard® Infusion Pump Systems, the company conducted additional flow-rate accuracy testing.

This testing revealed that some infusion sets do not meet the ±5% delivery accuracy for the system or the ±13% accuracy identified in the earlier recall notification (bd.com Therefore, the use of the pump system potentially could cause over-infusion or under-infusion of therapy and patient harm. Based on those test results CME America is providing additional information and customer actions regarding its previous recall to include all infusion sets used with the BodyGuard® infusion pump distributed beginning May 2016.

CME America has defined four categories of impacted infusion sets based on delivery inaccuracy variability, two of which (Category A and B) can continue to be used in accordance with the instructions in the recall letter (bd.com CME America also announced on April 27, 2020, the decision to suspend distribution of the BodyGuard® infusion pumps and to remove all existing products from the U.S. market. CME America will work with customers to address the latest expanded infusion set recall and will continue to maintain continuity of care during the COVID-19 pandemic. Until such time that the BodyGuard® pumps have been removed from the market, CMEA will supply accessories and infusion sets in "Category A" and "Category B" to support the infusion pumps, and customers can continue to use the products in accordance with the Operator's Manual and the additional mitigations outlined in the customer letter.

Affected Product Types:

- BodyGuard BodySet
- BodyGuard Microset with Needleless Adaptor
- BodyGuard Microsets
- BodyGuard Microset w/ Non-Vented Spike Connector
- BodyGuard set with Female Luer
- BodyGuard Microset w/ 0.2 mic filter and lower y-site with female luer
- BodyGuard Microsets with Filter
- Standard BodySet with Needleless Connectors
- BodyGuard Microset with Filter and Manual Priming Valve
- CMExpress Microbore Sets
- BodyGuard Microset with Male Luer Connectors
- CMExpress Needleless Y Site Microbore Set

Check the full recall details on fda.gov

Source: FDA
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Reported By SafelyHQ.com User

April 12, 2020 12:00 PM

“Details: McPherson County says the employee was not showing symptoms while on the clock, but started to feel sick and left work for the day.

Dillons says it's supporting the employee with emergency paid leave and discussed sanitation efforts it immediately took after learning of this case.

Rep ... See Moreort: 4/10/2020
Source: kwch.com
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Reported By SafelyHQ.com User

May 15, 2020 11:00 AM

“Company name: Summitt Labs
Brand name: KORE ORGANIC
Product recalled: Watermelon CBD oil tincture
Reason of the recall: Contains lead
FDA Recall date: May 15, 2020
Recall details: Summitt Labs is voluntarily recalling Batch#730 Lot#K018 of KORE ORGANIC Watermelon CBD Oil Tincture, 30 ml bottle ... See More, 15mg 450x to the consumer level. The Florida Department of Agriculture and Consumer Services tested a random sample and found the product to contain lead levels at 4.7 ppm. When informed of this, Summitt Labs issued an immediate voluntary recall and started an internal investigation. As part of this investigation Summitt Labs had a sample from Batch #730 Lot #K018 tested at an ISO/IEC accredited lab. Lead results were 500 ppb (.5ppm), which is within the legal limits as defined by the State of Florida. However, based on the test from the Florida Department of Agriculture and Consumer Services, Summitt Labs initiated, and will complete, a full recall of Batch #730 Lot #K018 in full cooperation with the FDA and Florida Department of Agriculture and Consumer Services.

Summitt Labs is an inspected and licensed facility under the Florida Department of Food and Agriculture and Consumer Services to produce products containing CBD but the Federal Food and Drug Administration does not consider CBD to be a legal drug or dietary supplement. Ingestion of KORE ORGANIC Watermelon CBD Oil Batch #730 Lot #K018 containing lead could result in high lead exposure. According to the Florida Department of Health, acute lead poisoning could have signs and symptoms including but not limited to; Pain, Muscle Weakness, Paresthesia, Abdominal Pain, Nausea, Vomiting, Diarrhea, Constipation, Poor appetite, Weight Loss, Symptoms associated with encephalitis, Metallic taste in the mouth, Shock, Hemolysis, and Kidney Damage. To this date, Summitt Labs has not had a call, complaint or report of any adverse effect from the use of this product.

The product labels states that benefits may include, Anxiety Relief, Pain Reduction, Mood Enhancer, Restful Sleep and may Alleviate Stress. The product is packaged in 30 milliliter bottles; which could come in 9 count displays in Kraft paper packaging. The affected Kore Organic Watermelon CBD Oil lots include Batch#730 Lot#K018. The Product can be identified by the Kore Organic Logo and Kraft Paper Packaging on the 30 milliliter bottle. The product was distributed nationwide by Wholesalers (I.E. Nirvana Kulture and North East Rally), Samples by Sales Personnel, Tradeshow Samples, and by Summitt Labs. Summitt Labs is notifying its distributors and customers by email, phone, and personal visits to ensure the return of all recalled product.

Consumers, distributors and retailers that have Kore Organic Watermelon CBD Oil Batch #730 Batch #K018, which is being recalled, should stop using the product. Any consumer with Lot #K018 Batch #730 should return this product to the place of purchase for a full monetary refund. If that is denied, please contact Summitt Labs at the above number for refund information and any other information regarding 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.

Check the full recall details on fda.gov

Source: FDA
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Reported By SafelyHQ.com User

June 5, 2020 9:34 AM

“They ignoring customers and giving us raw chicken. See Less
Reported By SafelyHQ.com User

June 22, 2020 11:34 AM

“Thanks for serving my cousin some raw chicken meat! One bite of raw ... See Moreelyhq.com/product/chicken#scroll" title="Product: Chicken">chicken meat wont hurt right? See Less
Reported By SafelyHQ.com User

July 13, 2020 5:32 AM

“I am so disgusted. Raw chicken 🥴🥴🥴🥴 See Less
Reported By SafelyHQ.com User

May 7, 2020 1:00 PM

“Company name: Becca Cosmetics
Brand name: Becca Cosmetics
Product recalled: Light Shifter Brightening Concealer
Reason of the recall: Potential Mold
FDA Recall date: May 07, 2020
Recall details: Company Announcement Out of abundance of caution, and in line with its commitment to consumer sat ... See Moreisfaction and safety, Becca Cosmetics is voluntarily recalling all shades of its Light Shifter Brightening Concealer because a brownish-black material identified as a common household mold was found on the sponge-tip applicator of some units. While this is unlikely to cause serious injury there is a potential risk of temporary skin and/or eye allergy and irritation.

To date, no adverse reactions or injuries have been reported. This product was manufactured in the United States and distributed nationwide. The below are the details of the product affected by this recall. No other Becca Cosmetics products are affected by this issue.

- Product Name: Becca Cosmetics Light Shifter Brightening Concealer
- Batch: 0030A, 9308A, 0052A, 0052C, 9291A, 9309A, 0036A, 0037A, 0038A, 0038B, 0041A, 9289A, 0062A, 0062B, 0062C, 9283A, 9284A, 9287A, 9288A
- Size: 3.2 mL (only size available)
- Product Description: Concealer wand with silver overlay, and a white secondary carton
- UPC: 9331137030037, 9331137030044, 9331137030051, 9331137030068, 9331137030075, 9331137030099, 9331137030082, 9331137030105

If you have this product, please stop using it and contact the place of purchase regarding a refund. 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

June 22, 2020 11:32 AM

“⁩ bought from this branch and in date to the 24th! Slices are slimy before finding it in really badly undercooked inside! Having suffered with E. coli a few years ago I am not prepared to go through that again 🤷‍♀️🤷‍♀️ See Less
Reported By SafelyHQ.com User

April 23, 2020 8:51 AM

“At least 6 employees at this location have tested positive for COVID 19. 5 other area awaiting results. If you were at this location within the last 2 weeks, please call Metro Health to report it. See Less
Reported By SafelyHQ.com User