Report by
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
NOTICE: For Coronavirus (COVID-19) information, alerts sign up, and to report your case go to https://safelyhq.com/tag/coronavirus-covid-19
Additional 2 employees confirmed positive for Covid-19, Teufel Holly Farms, 35600 NW Zion Church Rd, Cornelius, OR 97113, USA
Teufel Holly Farms, 35600 NW Zion Church Rd, Cornelius, OR 97113, USA
November 26, 2020 12:00 PM
“Additional 2 employees confirmed positive for Covid-19 at Teufel Holly Farms, Inc in Washington County. Investigation Start Date: 10/29/2020 , with the most recent onset of: 10/31/2020 New Cases of: 2
Source: www.oregon.gov See Less”
Helpful
Additional 5 employees confirmed positive for Covid-19, Target Distribution Center, 875 Beta Dr SW, Albany, OR 97321, USA
Target Distribution Center, 875 Beta Dr SW, Albany, OR 97321, USA
November 26, 2020 12:00 PM
“Additional 5 employees confirmed positive for Covid-19 at Target Distribution Center in Linn County. Investigation Start Date: 9/14/2020 , with the most recent onset of: 11/14/2020 New Cases of: 5
Source: www.oregon.gov See Less”
Helpful
Active Covid-19 outbreak of 6 employees, Swire Coca-Cola USA, 9750 SW Barber St, Wilsonville, OR 97070, USA
Swire Coca-Cola USA, 9750 SW Barber St, Wilsonville, OR 97070, USA
November 26, 2020 12:00 PM
“Active Covid-19 outbreak of 6 employees at Swire Coca-Cola USA in Clackamas County. Investigation Start Date: 11/05/2020 , with the most recent onset of: 11/16/2020 New Cases of: 6
Source: www.oregon.gov See Less”
Helpful
Active Covid-19 outbreak of 7 employees, Smith Frozen Foods, Inc., 101 E Depot St, Weston, OR 97886, USA
Smith Frozen Foods, Inc., 101 E Depot St, Weston, OR 97886, USA
November 26, 2020 12:00 PM
“Active Covid-19 outbreak of 7 employees at Smith Frozen Food in Umatilla County. Investigation Start Date: 11/17/2020 , with the most recent onset of: 11/11/2020 New Cases of: 7
Source: www.oregon.gov See Less”
Helpful
Additional 5 employees confirmed positive for Covid-19, Skyline Homes Inc, 550 SW Booth Bend Rd, McMinnville, OR 97128, USA
Skyline Homes Inc, 550 SW Booth Bend Rd, McMinnville, OR 97128, USA
November 26, 2020 12:00 PM
“Additional 5 employees confirmed positive for Covid-19 at Skyline Homes, Inc in Yamhill County. Investigation Start Date: 11/5/2020 , with the most recent onset of: 11/15/2020 New Cases of: 5
Source: www.oregon.gov See Less”
Helpful
Additional 2 employees confirmed positive for Covid-19, Roseburg Forest Products Co, 451 N Cedar Point Rd, Coquille, OR 97423, USA
Roseburg Forest Products Co, 451 N Cedar Point Rd, Coquille, OR 97423, USA
November 26, 2020 12:00 PM
“Additional 2 employees confirmed positive for Covid-19 at Roseburg Forest Products in Coos County. Investigation Start Date: 10/29/2020 , with the most recent onset of: 11/18/2020 New Cases of: 2
Source: www.oregon.gov See Less”
Helpful
Additional 3 employees confirmed positive for Covid-19, Rosboro, 2509 Main St, Springfield, OR 97477, USA
Rosboro, 2509 Main St, Springfield, OR 97477, USA
November 26, 2020 12:00 PM
“Additional 3 employees confirmed positive for Covid-19 at Rosboro Company, LLC in Lane County. Investigation Start Date: 11/3/2020 , with the most recent onset of: 11/16/2020 New Cases of: 3
Source: www.oregon.gov See Less”
Helpful
An additional 1 employee confirmed positive for Covid-19, Plycem USA, 1200 Ave G, White City, OR 97503, USA
Plycem USA, 1200 Ave G, White City, OR 97503, USA
November 26, 2020 12:00 PM
“An additional 1 employee confirmed positive for Covid-19 at Plycem USA LLC in Jackson County. Investigation Start Date: 11/2/2020 , with the most recent onset of: 11/6/2020 New Cases of: 1
Source: www.oregon.gov See Less”
Helpful
Additional 5 employees confirmed positive for Covid-19, Planasa Oregon Operations, 8383 Short Rd, Klamath Falls, OR 97603, USA
Planasa Oregon Operations, 8383 Short Rd, Klamath Falls, OR 97603, USA
November 26, 2020 12:00 PM
“Additional 5 employees confirmed positive for Covid-19 at Planasa Oregon Operations, LLC in Klamath County. Investigation Start Date: 10/1/2020 , with the most recent onset of: 11/16/2020 New Cases of: 5
Source: www.oregon.gov See Less”
Helpful
Additional 2 employees confirmed positive for Covid-19, Pacific Coast Fruit Company, 201 NE 2nd Ave, Portland, OR 97232, USA
Pacific Coast Fruit Company, 201 NE 2nd Ave, Portland, OR 97232, USA
November 26, 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: 11/15/2020 New Cases of: 2
Source: www.oregon.gov See Less”
Helpful
Recent Interesting Reports
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 See Less”
Helpful
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 See Less”
Helpful
1 person found this review helpful
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”
Helpful
5 people found this review helpful
Walmart Supercentre, Boulevard Maloney Ouest, Gatineau, QC, Canada, Walmart Supercentre, Boulevard Maloney Ouest, Gatineau, QC, Canada
Walmart Supercentre, Boulevard Maloney Ouest, Gatineau, QC, Canada
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”
Helpful
2 people found this review helpful
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”
Helpful
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”
Helpful
Covid-19 OSHA Complaint, Campbell City Hall, 70 North 1st Street, Campbell, CA 95008, USA
Campbell City Hall, 70 North 1st Street, Campbell, CA 95008, USA
November 25, 2020 12:00 PM
“Potential concern regarding implementing Center for Disease Control (CDC), Local Health Department and Cal/OSHA Guidance on Requirements to Protect Workers from Coronavirus to prevent the spread between person-to-person and close contact (within about 6 feet) while working and enforce wearing of fac... See Moree covering by all employees. Title 8 CCR Sections 3203 & 3380
Alleged Hazards: 1, Employees Exposed: 1
Source: Osha.gov | Receipt Date: 2020-11-05 See Less”
Helpful
Covid-19 OSHA Complaint, Ann Arbor Comprehensive Treatment Center, 522 S Maple Rd, Ann Arbor, MI 48103, USA
Ann Arbor Comprehensive Treatment Center, 522 S Maple Rd, Ann Arbor, MI 48103, USA
November 10, 2020 12:00 PM
“1) The employer is not following the ¿Stay Home¿ Executive Order in place. The company that owns the Ann Arbor Comprehensive Treatment Center, Acadia Healthcare, has not taken any measures to allow counselors to work from home. The counselors are mostly doing teletherapy but these employees are stil... See Morel required to be physically present in the clinic 40 hours a week and do face-to-face intakes and appointments with patients who do not have a phone. The employer has not implemented restrictions for limiting staff onsite and employees are not allowed to work remotely. This violates the "Promote remote work to the fullest extent possible" and "Restrict the number of workers present in-person on the job" sections of the Executive Order. On any given day there are five counselors working, receptionist, supervisor, clinic director, 2-3 nurses, and a part-time doctor. These employees are all required to be present in the building. 2) The receptionist does not wear a mask, nurses ran out of masks, and approximately 100 daily patients are not provided masks. Employees have been reusing the same (disposable) mask for weeks. 3) The patients do not practice the 6-foot social distancing rule. 4) A new patient tested positive for the coronavirus and is currently in the hospital. This patient was in the building for several hours on April 7, 2020. This building is not that big, and this patient was in the lobby, restroom, lab, dosing booth, doctor's office, and a smaller office to do paperwork.
Source: Osha.gov | Receipt Date: 2020-04-10 See Less”
Helpful
Covid-19 OSHA Complaint, Hope Network Center for Autism - East Lansing, 2875 Eyde Pkwy, East Lansing, MI 48823, USA
Hope Network Center for Autism - East Lansing, 2875 Eyde Pkwy, East Lansing, MI 48823, USA
November 10, 2020 12:00 PM
“The employer has a lax policy on maintaining employee health when exposed to infection. Three employees have become infected with Covid-19 as a result of management not enforcing safety standards with clientele. There are only twelve of us employees at this site, total.
Source: Osha.gov | Rece... See Moreipt Date: 2020-09-18 See Less”
Helpful
Additional 12 employees confirmed positive for Covid-19, OrePac Building Products, 30170 SW Ore Pac Ave, Wilsonville, OR 97070, USA
OrePac Building Products, 30170 SW Ore Pac Ave, Wilsonville, OR 97070, USA
November 12, 2020 12:00 PM
“Additional 12 employees confirmed positive for Covid-19 at OrePac Building Products in Clackamas County. Investigation Start Date: 10/30/2020 , with the most recent onset of: 11/3/2020 New Cases of: 12
Source: www.oregon.gov See Less”
Helpful