Create a Report
Please provide report title
Please provide location
Please provide details
Get alerts and updates for your case! Your contact information is not shown on the website.
This information is not shown on the website. We can notify you of updates, and may contact you for more information to help resolve or follow up on your issue.
Please provide email or phone
Please provide email or phone

We do not show your email or contact info

Please accept our Terms & Conditions
Add photos or video
We recommend photos and videos to help explain your report
Use camera
Select from library
Email or SMS copy of report
Enter below to get emailed a copy of your report, or sms a link to your report
Please provide email or phone
Please provide email or phone
Please accept our Terms & Conditions
Thank you for your report!
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)
Visit our learn pages for more helpful information or, email us: support@safelyhq.com
Goodbye! and best wishes in your recovery
Please provide location
Please provide location
Please provide report title
Please provide details
Please accept our Terms & Conditions
Get alerts and updates for your case! Your contact information is not shown on the website.

This information is not shown on the website. We can notify you of updates, and may contact you for more information to help resolve or follow up on your issue.

or
Please provide email or phone
Thank you for your report!

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)

If your report is poison related call 1-800-222-1222 for a free consultation with a live medical poisoning expert

Visit our learn pages for more helpful information or, email us: support@safelyhq.com

Goodbye! and best wishes in your recovery

Fayette County High School, 1 Tiger Trail, Fayetteville, GA 30214, USA

Total all time reports:  1
Latest report: April 15, 2020 12:00 PM
School food service worker tests positive for COVID-19, Fayette County High School, 1 Tiger Trail, Fayetteville, GA 30214, USA

School food service worker tests positive for COVID-19

April 15, 2020 12:00 PM

“A Fayette County High School food service department employee that was preparing and distributing meals tested positive for COVID-19 on April 10th.

Source: cbs46.com See Less
Reported By SafelyHQ.com User

Related Reports

August 9, 2020 12:00 PM

“A staff members at The Deck at Pere Marquette Park at 1601 Beach St. tested positive for COVID-19 at the end of July.

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

August 9, 2020 12:00 PM

“An employee at a Dairy Queen in West Duluth, located at 4431 Grand Ave tested positive for COVID-19 on Friday August 7.

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

Employee test positive for Covid-19, Hunter Lake Elementary School, 909 Hunter Lake Dr, Reno, NV 89509, USA

Hunter Lake Elementary School, 909 Hunter Lake Dr, Reno, NV 89509, USA

August 9, 2020 12:00 PM

“A Hunter Lake Elementary School staff member in Reno tested positive for COVID-19 on August 7.

Source: mynews4.com See Less
Reported By SafelyHQ.com User

Five confirmed cases of Covid-19, The Crossing at Union Cross Church, 1650 Pecan Ln, Winston-Salem, NC 27107, USA

The Crossing at Union Cross Church, 1650 Pecan Ln, Winston-Salem, NC 27107, USA

August 9, 2020 12:00 PM

“Three children and two staff members at the Crossing at Union Cross Church's Preschool Afterschool program in Kernersville have tested positive for Covid-19. All cases stem from exposure at the vacation bible school.

Source: wfmynews2.com See Less
Reported By SafelyHQ.com User

Employee test positive for Covid-19, Polson School District Superintendent, 111 4th Ave E, Polson, MT 59860, USA

Polson School District Superintendent, 111 4th Ave E, Polson, MT 59860, USA

August 9, 2020 12:00 PM

“An employee at the Polson School District summer meal program tested positive for COVID-19 on July 28

Source: See Less
Reported By SafelyHQ.com User

August 9, 2020 12:00 PM

“80 workers at O'Briens Fine Food in Co Kildare have tested positive for Covid-19.

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

August 9, 2020 12:00 PM

“A Broward school district employee at the K.C. Wright administrative building in Fort Lauderdale tested positive for the new coronavirus on August 7.

Source: sun-sentinel.com See Less
Reported By SafelyHQ.com User

Employee test positive for Covid-19, Joaquin Superintendent Office, 11109 U.S. 84, Joaquin, TX 75954, USA

Joaquin Superintendent Office, 11109 U.S. 84, Joaquin, TX 75954, USA

August 9, 2020 12:00 PM

“A Joaquin Independent School District employee tested positive for COVID-19 on Friday August 7 and multiple other employees are self-quarantining.

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

Employee test positive for Covid-19, The Catholic Diocese of Evansville, 4200 N Kentucky Ave, Evansville, IN 47711, USA

The Catholic Diocese of Evansville, 4200 N Kentucky Ave, Evansville, IN 47711, USA

August 9, 2020 12:00 PM

“A staff member at a Catholic Diocese of Evansville school tested positive for Covid-19 on August 8. The school the employee worked at was not identified.

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

Employee test positive for Covid-19, Cuyahoga Heights Schools, 4820 E 71st St, Cleveland, OH 44125, USA

Cuyahoga Heights Schools, 4820 E 71st St, Cleveland, OH 44125, USA

August 9, 2020 12:00 PM

“A trades crew member for the Heights Schools tested positive for COVID-19 last week on July 30.

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

Recent Interesting Reports

March 25, 2020 12:41 PM

“The company’s Soho location closed earlier this week. The employee who tested positive for COVID-19 was last in the Soho store on Tuesday, March 17, according to a company spokesperson. It’s still up-in-the-air when the Soho Trader Joe’s will reopen, but standard protocol is to close at least three ... See Moredays for cleaning.

“Out of an abundance of caution, we have temporarily closed the store for thorough cleaning and sanitization. As soon as the store has been fully cleaned and restocked, we plan to reopen,” Trader Joe’s said in an announcement on their website.
Source: ny.eater.com
See Less
Reported By SafelyHQ.com User

July 15, 2020 11:32 AM

“got a family dinner last night. 1 of the meals (chicken tenders) was under cooked very pink, so it wasn't eaten. Please make sure your cooks know raw ... See Moresafelyhq.com/product/chicken#scroll" title="Product: Chicken">chicken is a "no no". See Less
Reported By SafelyHQ.com User

July 22, 2020 6:01 PM

“Company name: Fresenius Kabi USA
Brand name: Fresenius Kabi
Product recalled: Dexmedetomidine Hydrochloride Injection, 200 mcg/50 mL
Reason of the recall: Cross contamination with lidocaine
FDA Recall date: July 22, 2020
Recall details: Fresenius Kabi USA is voluntarily recalling two lots of De ... See Morexmedetomidine 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 the possibility of a trace amount of lidocaine present in these two lots and our investigation indicates that this issue is limited to these two product lots. This recall is being performed to the user level.

To date, no adverse drug experience reports have been received for either of the lots being recalled by Fresenius Kabi. Administration of Dexmedetomidine HCl containing trace amounts of lidocaine to a patient with lidocaine allergy, however, could result in anaphylaxis, a potentially life-threatening condition. 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. Below there is a list of the recalled lots distributed nationwide to wholesalers, distributors, hospitals, and pharmacies between June 3, 2019 and April 8, 2020, as well as a copy of the label:

Product Name/Product size: 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: 6121853 - 6122207
Expiration Date: 05/2021 - 06/2021
First Ship Date 06/03/2019 - 12/04/2019
Last Ship Date: 03/12/2020 - 04/08/2020

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 any affected lots, 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
See Less
Reported By SafelyHQ.com User

June 4, 2020 12:03 PM

“Saturday June 6 in Tustin, Ca
At 4pm Mitchell and Newport
Meeting is at old Taco Bell 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
See Less
Reported By SafelyHQ.com User

May 20, 2020 10:00 PM

“Company name: Biota Biosciences, LLC
Brand name: Biota Biosciences
Product recalled: Cannabidiol (CBD) Complex, Curcumin Complex, Cannabidiol + Curcumin
Reason of the recall: Unapproved new drug
FDA Recall date: May 20, 2020
Recall details: Biota Biosciences is voluntarily recalling the followi ... See Moreng lots in the table below of Cannabidiol (CBD) Complex, Curcumin Complex, and Cannabidiol + Curcumin Injectables to the customer level. These injectable products are being recalled because they were marketed without FDA approval. The products claims on our website make these products unapproved new drugs. Further, the products are misbranded because the labeling fails to bear adequate directions for use.

- Product Name: Cannabidiol(CBD)Complex / Strength(mg): 40 / Multiple Dose Vial Size: 10 mL / Lot: 2H071219P / Expiration: 07/12/2021

- Product Name: Cannabidiol(CBD)Complex / Strength(mg): 500 / Multiple Dose Vial Size: 10 mL / Lot: 10102019P / Expiration: 10/10/2021

- Product Name: Curcumin Complex / Strength(mg): 40 / Multiple Dose Vial Size: 10 mL / Lot: 2H071219CCD / Expiration: 07/12/2021

- Product Name: Curcumin Complex / Strength(mg): 500 / Multiple Dose Vial Size: 10 mL / Lot: 0712019CCD / Expiration: 07/12/2021

- Product Name: Cannabidiol + Curcumin / Strength(mg): 500 / Multiple Dose Vial Size: 10 mL / Lot: 10102019PC / Expiration: 10/10/2021

Risk Statement: Unapproved new drugs injected into the bloodstream for which safety and efficacy have not been established could pose a serious risk of harm to users because they bypass many of the body’s natural defenses against toxic ingredients, toxins, or dangerous organisms that can lead to serious and life-threatening conditions such as septicemia or sepsis. Biota Biosciences has not received any reports of adverse events related to this recall.

Risk Statement: Unapproved new drugs injected into the bloodstream for which safety and efficacy have not been established could pose a serious risk of harm to users because they bypass many of the body’s natural defenses against toxic ingredients, toxins, or dangerous organisms that can lead to serious and life-threatening conditions such as septicemia or sepsis. Biota Biosciences has not received any reports of adverse events related to this recall.

Cannabidiol (CBD) Complex was marketed to suppress pain and aid in the detoxification processes as a promising therapeutic for a wide array of disorders such as epilepsy, including many challenging neuropathy conditions. Curcumin Complex was marketed as a potent anti-inflammatory and antioxidant that may also help improve symptoms of depression and arthritis. Cannabidiol + Curcumin was marketed as a more efficient therapeutic effect. The product was sold to certified practitioners who further administer to customers. The product is packaged in 10 mL sterile vials. Products were distributed Nationwide in the USA and one consignee in New Zealand.

Water Soluble 40mg/10m products can be identified by the labels attached.

Water Soluble 500mg/10m products can be identified by the labels attached.

Check the full recall details on fda.gov

Source: FDA
See Less
Reported By SafelyHQ.com User

July 6, 2020 11:30 PM

“Company name: J. M. Smucker Company
Brand name: Natural Balance
Product recalled: Ultra Premium Chicken & Liver Paté Formula
Reason of the recall: Due to elevated levels of choline chloride
FDA R ... See Moreecall date: July 03, 2020
Recall details: The J. M. Smucker Company today announced a voluntary recall of one lot of Natural Balance® Ultra Premium Chicken & Liver Paté Formula canned cat food due to health concerns likely associated with elevated levels of choline chloride. Ingesting impacted product may cause nausea with excessive salivation, constricted pupils and poor vision, diarrhea or vomiting to more severe symptoms including difficulty walking, muscle shaking, tremors, irregular heartbeat, difficulty breathing, possible cardiac or respiratory failure and, in extreme situations, death. Pet parents are encouraged to contact their cat’s veterinarian immediately if their cat is displaying any of these symptoms.

If pet parents have any product matching the following description in their possession, they should stop feeding it to their cats and dispose of the product. This information can be found on the bottom of each can.

- Natural Balance® Ultra Premium Chicken & Liver Paté Formula canned cat food (5.5 oz). UPC: 2363353227. Lot code: 9217803. Best by: 08 04 2021

These products are most commonly sold in pet specialty retailers and online throughout the United States and Canada. No other Natural Balance® products are impacted by this recall.

The Company has received reports of adverse reactions. Pet parents that have questions or would like to report adverse reactions should call 888-569-6828, Monday through Friday, 8 a.m. – 5 p.m. ET or email anytime at info@naturalbalanceinc.com.

Check the full recall details on fda.gov

Source: FDA
See Less
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

Chicken from Costco is almost raw, Costco Wholesale, 16580 NW 59th Ave, Hialeah, FL 33014, United States

Costco Wholesale, 16580 NW 59th Ave, Hialeah, FL 33014, United States

May 6, 2020 9:35 PM

“Translation:
Honestly, I love Costco, and I'm not trying to put any employee in a bad light, especially in the chicken-rotisserie area. I have a picture of how red hot it is on a piece of ... See Morebtn-link" href="https://safelyhq.com/product/meat#scroll" title="Product: Meat">meat and blood on the bones. Chickens need more fire and cooking.

Original:
Con sinceridad, amo Costco, y no trato de poner en mal a ningun empleado en especial la zona de los asadores de pollo. Tengo la foto lo rojo vivo que esta en una parte de la carne y sangre en los huesos. Los pollos necesitan mas fuego y cocimiento. See Less
Reported By SafelyHQ.com User

August 5, 2020 12:36 AM

“Company name: Roque Plast S.A. de C.V.
Brand name: Command Brands
Product recalled: Hand Sanitizer
Reason of the recall: Methanol Contamination
FDA Recall date: August 04, 2020
Recall details: Roque Plast S.A. de C.V. is voluntarily recalling lots 200371-12, 200371OH-05, 170420OH-06, 170420OH-8 ... See Moremanufactured by Roque Plast S.A. de C.V. of Command Brands Gel AntiBac Instant Hand Sanitizer to the consumer level. This recall has been initiated due purported potential presence of methanol indicated by the Food and Drug Administration (FDA) when product was presented for import in the United States. Although, final official FDA analysis results and reports have not been received, out to the abundance of caution and as suggested by the FDA, Roque Plast S.A. de C.V. are recalling lots 200371-12, 200371OH-05,170420OH-06,170420OH-8.

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 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 Roque Plast S.A. de C.V. has not received reports of adverse events related to the products of this recall.

Recalled Products:
Name product: Command Brands Gel AntiBac Instant Hand Sanitizer
NDC: 50058-100-08
Package formats (sizes):  8.4 fl oz (250 mL)
Plastic bottleUPC: 8_52239_00689_2
Affected lot (numbers):  200371-12, 200371OH-05, 170420OH-06, 170420OH-8

The product is used as a hand sanitizer for hand washing to decrease bacteria on the skin when soap and water are not available. The products are packaged in an 8.4 fl oz (250 mL) PET or High-density polyethylene (HDPE) plastic bottle with UPC 8_52239_00689_2. The product is labeled with a red, blue and yellow stripes with the words Command Brands Gel AntiBac Instant Hand Sanitizer written in yellow and blue letters. The product was distributed nationwide throughout the United States.

Roque Plast S.A. de C.V. is notifying its customers/distributors by recall letter and consumers via this press release.  We are also notifying our distributors, who will help notify their customers by phone calls, emails, and/or mailed letters and is arranging for return of all recalled products.

Consumers, distributors, and retailers that have product which is being recalled should stop use or distribution and return to place of purchase. Consumers should contact their physician or healthcare provider if they experienced any problems that may be related to taking or using this product.

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
See Less
Reported By SafelyHQ.com User