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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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Turkey

Updated: May 10, 2020 12:00 PM

May 10, 2020 12:00 PM

“Fenerbahçe was forced to cancel training sessions for Friday after an employee of the club tested positive for COVID-19.

The results from Thursday showed someone working at the team's premises was positive for COVID-19.

A second employee is also suspected of having the virus.

Source: https:... See More//www.dailysabah.com See Less
Reported By SafelyHQ.com User

Team employee tests positive for COVID -19, Zühtüpaşa, Fenerbahçe Şükrü Saraçoğlu Stadyumu, Recep Peker Cd. No.2, 34724 Kadıköy/İstanbul, Turkey

Zühtüpaşa, Fenerbahçe Şükrü Saraçoğlu Stadyumu, Recep Peker Cd. No.2, 34724 Kadıköy/İstanbul, Turkey

May 8, 2020 12:00 PM

“A Fenerbahçe employee working at the team's premises has tested positive for COVID -19

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

April 29, 2020 12:00 PM

“I have some mild symptoms of coronavirus. See Less
Reported By SafelyHQ.com User

March 10, 2020 9:29 AM

“6 sailors suspected cases Source: turkishmaritime.com.tr See Less
Reported By SafelyHQ.com User

Recent Interesting Reports

October 28, 2020 10:00 PM

“Company name: Whole Foods Market
Brand name: Whole Foods Market
Product recalled: Macaroni and Cheese products
Reason of the recall: Undeclared egg
FDA Recall date: October 28, 2020
Recall details: Whole Foods Market is voluntarily recalling select prepared Macaroni & Cheese products from store... See Mores across five states because they contain undeclared egg. People who have an allergy or severe sensitivity to egg run the risk of serious or life-threatening allergic reaction if they consume these products.

The affected products were sold at Whole Foods Market stores in Maryland, New Jersey, Pennsylvania, Virginia and Washington, D.C. The product was sold in plastic containers and in family-style meal kits with Whole Foods Market scale labels in the prepared foods department, available both hot and refrigerated. The product was also available from the chef’s case counter and from Whole Foods Market online and catering menus. The affected products can be identified by the following information. All affected product has been removed from store shelves. No allergic reactions have been reported to date.

- Macaroni & Cheese, chef’s case. Product Code (begins with) M: 286501. Best by 10/28/2020
- Macaroni & Cheese, packaged. Product Code (begins with) M: 263608. Best by 10/27/2020
- Macaroni & Cheese, online and catering. Product Code (begins with) M: 114449 | 109866. Best by 10/23/2020
- Rotisserie Chicken Meals with Mac & Cheese and Broccoli, packaged. Product Code (begins with) M: 261596 | 261580 | 261590 | 261601 | 261608 | 261616. Best by 10/26/2020
- Fried Chicken Meal with Mac & Cheese, packaged. Product Code (begins with) M: 247257. Best by 10/25/2020
- Fried Chicken Meal with Mac & Cheese, packaged on hot bar. Product Code (begins with) M: 237444. Best by 10/24/2020
- Chicken Rustico Romano Chef Plate with Mac & Cheese and Broccoli, packaged. Product Code (begins with) M: 241442. Best by 10/28/2020
- Chicken Breast Chef Plate with Mac & Cheese and Broccoli, packaged. Product Code (begins with) M: 299430. Best by 10/28/2020
- BBQ Turkey Meatballs Chef Plate with Mac & Cheese and Green Beans, packaged. Product Code (begins with) M: 241464. Best by 10/28/2020
- Roasted Turkey Chef Plate with Mac & Cheese and Broccoli, packaged. Product Code (begins with) M: 242019. Best by 10/28/2020

Customers who purchased this product at Whole Foods Market can bring a valid receipt into stores for a full refund. Consumers with additional questions can call 1-844-936-8255 between the hours of 7:00 a.m. and 10:00 p.m. CST, Monday through Friday, or 8:00 a.m. and 6:00 p.m. Saturday through Sunday.

Check the full recall details on fda.gov

Source: FDA
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Reported By SafelyHQ.com User

November 19, 2020 6:01 PM

“Company name: Fresenius Kabi USA
Brand name: Fresenius Kabi USA
Product recalled: Dexmedetomidine HCL in 0.9% Sodium Chloride Injection
Reason of the recall: Cross Contamination with Lidocaine
FDA Recall date: November 19, 2020
Recall details: Fresenius Kabi USA is voluntarily recalling a singl... See Moree lot of Dexmedetomidine HCl in 0.9% Sodium Chloride Injection, 200 mcg/50 mL (4 mcg /mL), 50 mL fill in a 50 mL vial. Fresenius Kabi initiated this recall due to a trace amount of lidocaine present in the lot. This recall is being performed to the user level. To date, no adverse drug experience reports have been received for the recalled lot. Administration of Dexmedetomidine HCl containing trace amounts of lidocaine to a patient with lidocaine allergy could result in a potentially life-threatening allergic reaction. 

Dexmedetomidine Hydrochloride in 0.9% Sodium Chloride Injection is approved for intravenous use and indicated for sedation of non-intubated patients prior to and/or during surgical and other procedures. Listed below is a table of the recalled lot distributed nationwide to wholesalers, distributors, hospitals and pharmacies between April 9, 2020 and April 13, 2020. An image of the label is also included below.

- Dexmedetomidine HCl in 0.9%. Sodium Chloride Injection, 200 mcg / 50 mL (4 mcg / mL), 50 mL fill in a 50 mL vial. NDC Number: 63323-671-50. Product Code: 671050. Batch number: 6123925. Expiration Date: 03/2022. First Ship Date: 04/09/2020. Last Ship Date: 04/13/2020

Fresenius Kabi is notifying its distributors and customers by letter and asking them 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 any affected lots, and to return the product to Fresenius Kabi.

Customers with questions regarding this recall may contact Fresenius Kabi at 1-866-716-2459 Monday through Friday, during the hours of 8:00 a.m. to 5:00 p.m. Central Time. Consumers should contact their physician or health care 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
See Less
Reported By SafelyHQ.com User

November 9, 2020 5:00 PM

“Company name: Lohxa, LLC
Brand name: Lohxa
Product recalled: Chlorhexidine Gluconate Oral Rinse USP, 0.12% Alcohol free
Reason of the recall: May be contaminated with Burkholderia lata
FDA Recall date: November 09, 2020
Recall details: Lohxa, LLC is voluntarily recalling Chlorhexidine Gluconat... See Moree Oral Rinse USP, 0.12% Alcohol free (NDC:70166-027-15) products bearing an expiration date from 01/31/21 – 03/31/21 (see specific lots below) to the consumer level. This product is sourced and repackaged from Sunstar Americas Inc. who has notified us the product may be contaminated with the bacteria Burkholderia lata.

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, no adverse events have been reported to Lohxa, LLC related to this recall.

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

- Chlorhexidine Gluconate Oral Rinse USP, 0.12% Alcohol free is distributed in cases each containing 50 unit dose cups. Each case contains a colored label around the lid and body of the case.

The product can be identified by as shown in the images below. Chlorhexidine Gluconate Oral Rinse USP, 0.12% Alcohol free was distributed to Nationwide to hospital pharmacies. Lohxa, LLC is notifying its direct customers by Fedex overnight mail, electronic mail, phone call 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 Lohxa, LLC by phone at 1-800-641-5564 or email info@lohxa.com on Monday-Friday from 8am-5pm EST. 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:

- Chlorhexidine Gluconate Oral Rinse USP, 0.12% Alcohol free, 15 mL (NDC:70166-027-15) LOT/ EXP: T09101A/01/2021 |T08292A/02/2021 |T10011A/02/2021 |M10193A/03/2021 |T10223A/03/2021

Check the full recall details on fda.gov

Source: FDA
See Less
Reported By SafelyHQ.com User

November 15, 2020 8:18 PM

“They are practically forcing people to put hand sanitizer on their hands even though they are not required to do so. I am allergic to some of the stuff because I don't know what's in their hand sanitizer and my hands got all cracked and chapped. They still practically forced people to do it even tho... See Moreugh there's no law. See Less
Reported By SafelyHQ.com User

October 28, 2020 11:00 AM

“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: October 28, 2020
Recall details: Sunstar Americas, Inc. (SAI) is voluntarily... See Morerecalling Paroex® Chlorhexidine Gluconate Oral Rinse USP, 0.12% products bearing an expiration date from 6/30/22 – 9/30/22 (see specific lots below) to the consumer level. This product may be contaminated with the bacteria Burkholderia lata.

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, no adverse events have been reported to SAI 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 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 by 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 are detailed in the link below.

Check the full recall details on fda.gov

Source: FDA
See Less
Reported By SafelyHQ.com User

They do not report positive COVID cases, In-N-Out Burger Distribution Center, Hamburger Lane, Baldwin Park, CA, USA

In-N-Out Burger Distribution Center, Hamburger Lane, Baldwin Park, CA, USA

October 31, 2020 12:15 AM

“I am a Butcher for the In N Out Meat Department in Baldwin Park. They do not report positive COVID cases. They just recently began social distance. Supervisor and managers and associates are covid positive or with symptoms. One associate has lost his sister to covid. He was never quarantined. In n o... See Moreut burger is responsible for a big part in the spread of the virus all across California. See Less
Reported By SafelyHQ.com User

November 12, 2020 12:00 PM

“Additional 1 employees confirmed positive for Covid-19 at Clint Newell Auto Group in Douglas County. Investigation Start Date: 10/31/2020 , with the most recent onset of: 11/5/2020 New Cases of: 1

Source: www.oregon.gov See Less
Reported By SafelyHQ.com User

Covid-19 OSHA Complaint, Salem Kidney Center, 2705 Boulder Park Court, Winston-Salem, NC 27101, USA

Salem Kidney Center, 2705 Boulder Park Court, Winston-Salem, NC 27101, USA

November 10, 2020 12:00 PM

“Employees could have been exposed to the COVID-19 virus in the workplace, due to employees not being informed when the first employee tested positive for the virus. The number of employees testing positive is increasing, yet employees with symptoms are still being told to come to work.


Source:... See MoreOsha.gov | Receipt Date: 2020-10-23 See Less
Reported By SafelyHQ.com User

Covid-19 OSHA Complaint, McHenry County Valley Hi Nursing Home, 2406 Hartland Rd, Woodstock, IL 60098, USA

McHenry County Valley Hi Nursing Home, 2406 Hartland Rd, Woodstock, IL 60098, USA

November 10, 2020 12:00 PM

“Kitchen: Employees are being exposed to COVID-19 while working in the facility. Employer has not implemented CDC guidelines, specifically requiring personal protective equipment be be worn (face masks and gloves). Applicable OSHA Standard: 5(a)(1) of the OSH Act and 29 CFR 1910.132. Kitchen: Employe... See Morees are exposed to wet and unsanitary floors creating slip and trip hazards. Applicable OSHA Standard: 29 CFR 1910.22

Alleged Hazards: 2, Employees Exposed: 1
Source: Osha.gov | Receipt Date: 2020-10-13
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Reported By SafelyHQ.com User

Covid-19 OSHA Complaint, Macy's, 2075 Festival Plaza Drive, Las Vegas, NV 89135, USA

Macy's, 2075 Festival Plaza Drive, Las Vegas, NV 89135, USA

November 10, 2020 12:00 PM

“1. Failure to comply with the mandate for persons/patrons to wear face coverings while in the Employer¿s business establishment. Staff is not requiring customers to wear facemasks. 2. The business is not limiting the number of customers that come in to the business. HAZARD LOCATION: Throughout the s... See Moretore 08/07/2020 KR

Alleged Hazards: 1, Employees Exposed: 1
Source: Osha.gov | Receipt Date: 2020-08-06
See Less
Reported By SafelyHQ.com User