Create a Report
Please provide report title
Please provide location
Please provide details
Get alerts and updates for your case!
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
Add Photo/Video
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 to process your report.


Email us at support@safelyhq.com if you have questions.

Report by
Loading...
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)

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

Goodbye! and best wishes in your recovery

2 employees tested positive for Covid-19, Walmart Distribution Center,2650 US-395, Hermiston, OR 97838

2 years ago

2650 U.S. 395, Hermiston, 97838 Oregon, United States

2 employees tested positive for Covid-19 at Walmart Distribution Center in Umatilla County. Investigation Start Date: 2021-04-26, with the most recent onset of: 2021-07-30 New Cases of: 2

Source: www.oregon.gov

10


Related Reports

Nestlé USA has announced a recall of 440,500 Starbucks-branded ceramic mugs due to safety concerns. The mugs, which have a metallic coating, pose a burn and laceration hazard if microwaved or filled with extremely hot liquid. The company has reported 12 incidents of the mugs overheating or... See More breaking, resulting in 10 injuries. Nestlé USA is currently working closely with the U.S. Consumer Product Safety Commission on this recall.

The recalled mugs were sold in two sizes, 11 oz. and 16 oz., as part of four different gift sets during the 2023 holiday season. They were distributed at Target, Walmart, and Nexcom (military retail outlets) across the U.S. from November 2023 to January 2024. The recall does not affect any other Nestlé USA or Starbucks-branded products.

- Starbucks Holiday Gift Set with 2 Mugs (11 oz.). Retailer: Target.
- Starbucks Classic Hot Cocoa and Ceramic Mug (16 oz.). Retailers: Walmart, Nexcom.
- Starbucks Peppermint and Classic Hot Cocoa Ceramic Mug (16 oz.). Retailer: Target.
- Starbucks Holiday Blend Coffee and Mug (16 oz.). Retailers: Walmart, Nexcom.

In case you experience harm from this product, it is important to report it. It can help to detect & resolve issues and prevent others from being harmed, and it enables better surveillance. If symptoms persist, seek medical care.

Source: nestleusa.com
See Less
304


I received the package from Katie Sanchez, 135 Raritan Center Pkwy, Edison, NJ. Package was addressed to a name I don't know but at my address. I did not order anything from Walmart or Amazon. Package contained a pillow in the shape of a flower, appears to be gently used. See Less
304


Brassica Pharma Pvt. Ltd. is voluntarily recalling the Eye Ointment products listed below with expiration dates ranging from February 2024 to September 2025. The products are being recalled due to a lack of sterility assurance. These products were distributed nationwide to wholesalers, retailers, and via the product... See More distributors, Walmart, CVS, and AACE Pharmaceuticals Inc. To date, Brassica Pharma Pvt. Ltd. has not received any reports of adverse events up to 16th February 2024 related to this recall.

For those patients who use these products, there is a potential risk of eye infections or related harm. These products are intended to be sterile. Ophthalmic drug products pose a potentially heightened risk of harm to users because drugs applied to the eyes bypass some of the body’s natural defenses.

The affected products are:
- Product Name: Equate Lubricant Eye Ointment (Mineral Oil 42.5%, White Petrolatum 57.3%, Lanolin Alcohols), Package Description: 3.5-gram tube, packaged in a cardboard box, Brand Name: Equate, NDC: 79903-026-35, UPC Code: 681131395298.
- Product Name: Equate Stye Lubricant Eye Ointment (Mineral Oil 31.9%, White Petrolatum 57.7%, Microcrystalline Wax, Stearic Acid, Wheat Germ Oil), Package Description: 3.5-gram tube, packaged in a cardboard box, Brand Name: Equate, NDC: 79903-028-35, UPC Code: 681131395304.
- Product Name: CVS Health Lubricant Eye Ointment (Mineral Oil 31.9%, White Petrolatum 57.7%, Microcrystalline Wax, Stearic Acid Wheat Germ Oil, Package Description: 3.5-gram tube, packaged in a cardboard box, Brand Name: CVS Health, NDC: 76168-707-35, UPC Code: 050428634141.
- Product Name: Lubricant PM Ointment, Package Description: 3.5-gram tube, packaged in a cardboard box, Brand Name: AACE Pharmaceuticals, NDC: 71406-124-35, UPC Code: 371406124356.
For Lot number and expiry dates, you can visit the link below.

Brassica Pharma Pvt. Ltd. Is notifying its distributors AACE Pharmaceuticals Inc and its retailers Walmart and CVS. These distributors shall be further notifying the wholesalers and retailers via mail of this recall and arranging for return of all impacted products listed above. Consumers, distributors and retailers that have any product which is being recalled should cease distribution of the product. Consumers should stop using the recalled Eye Ointment and may return any of the above listed products to the place of purchase.

In case you experience harm from this product, it is important to report it. It can help to detect & resolve issues and prevent others from being harmed, and it enables better surveillance. If symptoms persist, seek medical care.

Company name: Brassica Pharma Pvt. Ltd.
Brand name: Multiple brands
Product recalled: Eye ointment products
Reason of the recall: Due to Potential Lack of Sterility Assurance.
FDA Recall date: February 26, 2024

Source: fda.gov
See Less
303


San Luis, AZ, G.A. Mart dba H&Natural, is voluntarily recalling 2 lots of H&NATURAL TejoRoot, 10g pills, and 2 lots of H&NATURAL Brazil Seed, .167g Seeds to the consumer level. The products have been found via random FDA testing to contain yellow oleander, a poisonous plant native... See More to Mexico and Central America. H&NATURAL TejoRoot and H&NATURAL Brazil Seed were distributed Nationwide to via internet on their site, Amazon.com, and Walmart.com. The company has received one report of gastrointestinal illness, including painful symptoms in conjunction with internal bleeding in connection with H&NATURAL TejoRoot, and has not received any reports of adverse events in connection with H&NATURAL Brazil Seed.

Risk Statement: Ingestion of yellow oleander can cause neurologic, gastrointestinal, and cardiovascular adverse health effects that may be severe, or even fatal. Symptoms may include nausea, vomiting, dizziness, diarrhea, abdominal pain, cardiac changes, dysrhythmia, and more.

The recalled dietary supplements can be identified by the H&NATURAL logo and the following descriptions:
- Tejo Root, Raiz de Tejocte, H&Natural, Healthy, and Natural, Dietary Supplement, 10g pills, is packaged in a box or bottle, with UPC (196852946921)
- Brazil Seed Pure Natural Semilla de Brasil, H& Natural, Healthy and Natural, 0.167g seeds, packaged in a box or bottle, with UPC (195893047529) (196852820641) (195893698721) (195893236893)(196852134618) (195893336975)

Recalled lots are labeled with the following expiration dates, 3/24 and 5/24.

Consumers that have the recalled H&NATURAL TejoRoot or H&NATURAL Brazil Seed lots should stop using the products. 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.

In case you experience harm from extraneous materials, it is important to report it. It can help to detect & resolve issues and prevent others from being harmed, and it enables better surveillance. If symptoms persist, seek medical care.

Company name: G.A. Mart dba H&Natural
Brand name: H&Natural
Product recalled: Brazil Seed Pure Natural Semilla de Brasil & Tejo Root, Raiz de Tejocte
Reason of the recall: Product contains yellow oleander, a poisonous plant
FDA Recall date: February 23, 2024

Source: fda.gov
See Less
303


I ordered a 4XL Tshirt from Walmart.com and received a size Large Tshirt from Charles Kosanke in Katy, TX. This shirt was NOT what I ordered. I've reported it with Walmart.com and the seller with no response. See Less
2


An early morning power outage occurred near the surrounding area of East Main Street on Monday, Sept. 4. According to the Umatilla Electric Cooperative website, the power outage began around 1:57 a.m. and was reported to have fully restored power of all homes and businesses affected by... See More the outage at 11:28 a.m.

Outage link: outageviewer.umatillaelectric.com
Source: hermistonherald.com
Published: 2023-09-04
See Less
10


1 employee tested positive for Covid-19 at Walmart Distribution Center in Umatilla County. Investigation Start Date: 26-04-2021, with the most recent onset of: 03-01-2022 New Cases of: 1

Source: www.oregon.gov See Less
10


Recent Interesting Reports

I received a bottle labeled Verti from “Fulfilment Center, 14100 McCormick Drive, Tampa, FL 33626.” I did not order it ! See Less
70


I got a small package containing an item I do not recognize or have any clue what it does. There is an on/off switch and two red lights come on. I felt a small pain in my head when they came on. I did a google lens search and could not find any information on it. See Less
9


I received a package UPS, USPS, lightweight package from Jane 371 Little Falls Rd. Suite 4 Cedar Grove, NJ 07009 UPS tracking number 9248790344491184000909****
At least that I’m aware I did not order. See Less
747


Endo International plc announced today that one of its operating companies, Par Pharmaceutical, Inc. (Par), is voluntarily recalling one lot of Treprostinil Injection 20mg/20mL (1mg/mL) to the consumer level. The product is being recalled due to the potential for the presence of silicone particulates in the product... See More solution. The lot was distributed nationwide to wholesalers and hospitals from June 16, 2022, through October 17, 2022. To date, Par has not received any reports of adverse events related to this recall.

Administration of an injectable product that contains particulate matter may result in local irritation or swelling in response to the foreign material. If the particulate matter reaches the blood vessels it can travel to various organs and block blood vessels in the heart, lungs, or brain which can cause stroke and even lead to death.

Treprostinil Injection is formulated for subcutaneous or intravenous infusion. The product is a prostacyclin vasodilator indicated for the treatment of pulmonary arterial hypertension to diminish symptoms associated with exercise and for patients who require a transition from epoprostenol to reduce the rate of clinical deterioration.

Treprostinil Injection 20mg/20mL (1mg/mL) is distributed in 20mL multidose vials as sterile solutions in water for injection, individually packaged in cartons under NDC #42023-206-01. Only Lot 57014, expiration date 04/2024 is affected by this recall. Vials from the affected lot bear the attached label.

Par is providing written notification to wholesale accounts and the hospital location that has received the affected lot and is arranging for the return of all existing inventory of Lot 57014 through Inmar, Inc. Wholesale distributors and hospital pharmacies that have the product being recalled should immediately discontinue the use and stop distribution immediately.

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.

In case you experience harm from this product, it is important to report it. It can help to detect & resolve issues and prevent others from being harmed, and it enables better surveillance. If symptoms persist, seek medical care.

Company name: Endo International, Par Pharmaceutical
Brand name: Par Pharmaceutical
Product recalled: Treprostinil 20mg/20mL Injection
Reason for the recall: Potential Presence of Silicone Particulate Matter
FDA Recall date: March 12, 2024

Source: fda.gov
See Less
303


I didn't order this Bee Venom from Geathers Fottys 3646 W. Wolcott Ave., Chicago, IL 60609 USA See Less


I ordered it once and they have kept sending it and charging my bank and I can’t seem to stop it.

ACV Fast Formula . I keep receiving keto ACV gummies and keep getting charged and there appears to be no way to stop them… my bank... See More says I have to try to contact them but there is no phone or e-mail … ony a Las Vegas P.O. Box 81078.. this has been going on See Less
1.4K


I received a package containing a pair of sunglasses that I didn’t order from: Heather’s Motty
2207 Summit ave. Union City NJ 07087 See Less
174


I received a package/ring that I never ordered, claiming it was a 1 carat. Asking me to scan the QR code to register it. I did not register it because I was afraid of being charged for something that I did not order or scared that if I did scan it, but location on my phone would be tracked. See Less
173


I received a package from 895 Meyerside Drive; Mississauga, Ont. L5T 1R8, but no phone number. It has my name, address and phone number on it. I noticed someone else on Reddit had received an unsolicited package from the same address. See Less
47


Last 30 days