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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: Fruit

Updated: October 22, 2020 7:00 PM

October 22, 2020 7:00 PM

“Company name: COMERCIAL MEXICANA INNTERNATONAL INC
Brand name: TROPIQUE
Product recalled: ASSORTED FRUIT JELLY BAG & JELLY ANIMAL JAR
Reason of the recall: Potential Choking Hazard
FDA Recall date: October 22, 2020
Recall details: FDA Announcement Comercial Mexicana International Inc. in... See MoreBethpage New York is recalling the product because it may pose a choking hazard. Small jelly cups containing seaweed extract (carrageenan) has been identified as a potential choking hazard in children No incidents of consumers choking have been reported to date in connection with this problem. The potential choking hazard was discovered during a routine inspection by the New York State Department of Agriculture and Markets, Food Safety and inspection. The recalled jelly cups were sold in NY, NJ, CT, PA retail stores. The recall products are:
Check the full recall details on fda.gov
Source: FDA
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Reported By SafelyHQ.com User

October 21, 2020 12:00 PM

“Additional 4 employees confirmed positive for Covid-19 at Pacific Coast Fruit in Multnomah County. Investigation Start Date: 6/22/2020 , with the most recent onset of: 10/5/2020 New Cases of: 4

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

October 21, 2020 12:00 PM

“Unknown number of employees() at NORTHERN EDGE NAVAJO CASINO in FRUITLAND, NM tested positive for Covid-19. Event Date: 10/19/2020, RR-4421

Source: env.nm.gov See Less
Reported By SafelyHQ.com User

October 14, 2020 12:00 PM

“Active Covid-19 outbreak of 6 employees at Diamond Fruit Growers in Hood River County. Investigation Start Date: 10/7/2020 , with the most recent onset of: 10/7/2020 New Cases of: 6

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

Covid-19 OSHA Complaint, Harrah's Lake Tahoe, 15 U.S. 50, Stateline, NV 89449, United States

Harrah's Lake Tahoe, 15 U.S. 50, Stateline, NV 89449, United States

October 13, 2020 12:00 PM

“1. Hot water is not available for employees to wash their hands with that work in McLennan's Sports Bar. There has been no hot water for the last two months.
2. Bartenders working in McLennan's Sports Bar are standing/working in approximately 1 inch of water on a daily basis.
3. Mold is growin... See Moreg on the orange painted wall inside McLennan's Sports Bar. Every so often, the employer paints over the mold, but does not remove it. Employees are developing respiratory issues due to working around the mold.
4. Plug in fans are used in McLennan's Sports Bar due to poor ventilation. In turn, the fans are displacing and blowing the mold into the air resulting in employees developing respiratory issues.
5. Draught beer dispensers are not working properly resulting in the harborage of fruit flies and other insects.
6. The employer has not established work practices to ensure employees can effectively socially distance when working in public spaces to help prevent the spread of COVID-19.

Alleged Hazards: 6,
Source: Osha.gov | Receipt Date: 2020-09-10
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Reported By SafelyHQ.com User

October 12, 2020 12:00 PM

“An employee of the Fruit Basket Marketplace on Granite Street recently became symptomatic and tested positive for the coronavirus and anyone who was in the store between Oct. 2 and Oct. 11 was possible exposed.

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

October 1, 2020 12:00 PM

“3 individuals at Mountain Man Nut & Fruit Co. in Douglas county tested positive for Covid-19. The outbreak began on 9/25/20

Source: colorado.gov See Less
Reported By SafelyHQ.com User

September 17, 2020 12:00 PM

“Additional 1 employees confirmed positive for Covid-19 at Willamette Valley Fruit Company in Marion County. Investigation Start Date: 8/4/20 , with the most recent onset of: 8/31/20 New Cases of: 1

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

September 12, 2020 9:00 AM

“Report date: Sep 8, 2020
16. Food-contact surfaces: cleaned & sanitized
- comments: observed ice machine bin a little dirty located in bar area. Instructed to clean, sanitize and maintain at all times.

21. Proper hot holding temperatures
- comments: observed approximately 2. 5lbs of cooke... See Mored grilled chicken located in hot hold unit in chicken/salad prep area at improper hot holding during time of inspection. Noted temperature of mixed chicken parts ranging from 109. 5f-118. 0f. Instructed to hold all hot held food items at 135. 0f or higher at all times. Manager discarded voluntarily during this time. Priority violation. 7-38-005. Citation issued.

36. Thermometers provided & accurate
- comments: unable to locate thermometers in all cold hold units on premise to show internal temperatures of equipment. Must provide and maintain.

36. Thermometers provided & accurate

38. Insects, rodents, & animals not present
- comments: observed approximately 100 small black live flies flying throughout chicken/salad/deli,sushi and bakery prep areas, on premise during time of inspection. They are as follows. . . In all said areas of facility on the walls, ceilings directly above prep tables, on in use surfaces of prep tables (must clean and sanitize), on exterior surfaces of refrigeration units, on all exposed handsinks, on fruit display casing where cantaloupe and watermelon are stored, and in bar area near both handsink, beer tap handles and on dried glassware. Instructed to contact pest control for service and locate the source. Must minimize small black live activity in facility prep areas. Priority foundation violation. 7-38-020 (a). Citation issued.

Source: chicago.gov
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Reported By SafelyHQ.com User

September 10, 2020 12:00 PM

“Additional 2 employees confirmed positive for Covid-19 at Pacific Coast Fruit in Multnomah County. Investigation Start Date: 6/22/2020 , with the most recent onset of: 9/3/2020 New Cases of: 2

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

Recent Interesting Reports

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
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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
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Reported By SafelyHQ.com User

November 23, 2020 2:00 PM

“Company name: Fusion Health and Vitality LLC
Brand name: CORE, Immune Boost
Product recalled: CORE essential nutrients and Immune Boost Sublingual Vitamin D3
Reason of the recall: Unapproved new drug
FDA Recall date: November 23, 2020
Recall details: Fusion Health and Vitality LLCis voluntaril... See Morey recalling all 2020 Lots of CORE essential nutrients and Immune Boost Sublingual Vitamin D3. CORE has been found to contain an unapproved food additive, hordenine HCl, rendering it adulterated. Immune Boost Labeling was found to contain statements that caused it to become and unapproved new drug under FDA labeling laws. Hordenine HCl is possibly unsafe when taken by mouth. Hordenine HCl might have similar stimulant effects and side effects such as rapid heart rate and high blood pressure.

Fusion Health and Vitality LLC has not received any reports of adverse events related to this recall.  Please review the attached photos for identification. We began shipping Core Essential Nutrients on 1/2/2020 and we began shipping Immune Boost Sublingual Vitamin D3 on 4/15/2020. Both products are packaged with labels which prominently display the product name.  CORE essential nutrients are found in a dark colored jar, in powdered format. 

This product was formulated to mix into a liquid before consumption. The Immune Boost sublingual was packaged in a 2 ounce bottle that came with a sublingual application dropper. Fusion Health and Vitality is notifying its customers by email and is arranging for return of all recalled products. Consumers that have product which is being recalled should stop using it and return it to Fusion Health and Vitality for destruction. Consumers with questions regarding this recall or how to return recalled product can contact Fusion Health and Vitality by calling 1-888-964-5327, 9am to 5pm, Monday Thru Friday, EST. 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.

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

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 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
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Reported By SafelyHQ.com User

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 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

Covid-19 OSHA Complaint, Commodore Homes of Indiana, 1902 Century Drive, Goshen, IN 46526, USA

Commodore Homes of Indiana, 1902 Century Drive, Goshen, IN 46526, USA

November 18, 2020 12:00 PM

“They are having employees go back to work that have tested positive for COVID-19 before they have completed quarantine. The employees returning to work who have tested positive are exposing other employees. They are threatening their jobs if they do not go back. They are not letting employees know w... See Morehich departments have tested positive. They have over 10 employees that have tested positive for COVID-19. The mudding department had employees test positive. They shut down the mudding department for 14 days but most of the employees had to come back after 5 days. They have had employees in the cabinet deptartment, the roof department, and the final department that tested positive and they have not shut down. Some employees have tested positive and they pointed them out and fired them. They do not always use safety nets while they are up on the roof, employees are not tied off when they are on the roof.


Source: Osha.gov | Receipt Date: 2020-06-26
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Reported By SafelyHQ.com User

Covid-19 OSHA Complaint, Quandel Group, 224 Wyoming Ave, Scranton, PA 18503, United States

Quandel Group, 224 Wyoming Ave, Scranton, PA 18503, United States

November 25, 2020 12:00 PM

“1) Several employees at the job site have tested positive for the corona virus. The GC is not taking steps to ensure the safety of the workers, including enforcing social distancing and the use of face coverings.


Source: Osha.gov | Receipt Date: 2020-10-26 See Less
Reported By SafelyHQ.com User

Covid-19 OSHA Complaint, Walmart Supercenter, 1807 West Craig Road, North Las Vegas, NV 89032, USA

Walmart Supercenter, 1807 West Craig Road, North Las Vegas, NV 89032, USA

November 10, 2020 12:00 PM

“1. Employees are concerned about a rotten egg smell emanating from the deli/bakery area. Employees have reported headaches after working in the area. HAZARD LOCATION: Deli and bakery area. 8/18/2020 JH

Alleged Hazards: 1,
Source: Osha.gov | Receipt Date: 2020-08-12 See Less
Reported By SafelyHQ.com User