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Ordered 2 GTA chainsaws and got 2 chainsaw blades, Auburn, NY, USA
December 27, 2020 3:02 PM
Auburn, 13021 New York, United States
False advertising misleading GTA 26 was ordered only received blades pictures of item was not item that I received
January 18, 2021 1:56 PM
“I ordered the hand held cutter and received something not related to my order. Take them DOWN NOW ”
Scurry, TX, USA
January 19, 2021 2:01 PM
“Purchased a Stihl wood cutter, received some off brand. Cannot get in touch to return for a refund. Definitely a scam. Sad that i don't want to order off of Face Book any more. ”
Evansville, IN, USA
January 19, 2021 5:06 PM
“Ordered chainsaw....only received a chain. Take this sight off pinterest. They're frauds. ”
Laurel, MT, USA
January 19, 2021 9:02 PM
“I pd for and did not receive 2 battery operated chain saws for both brothers for CHRISTMAS waited and seen where the money was taken from my account, NEVER RECEIVED THEM. SCAMMERS. NEVER AGAIN WILL I TRUST THIS CO. ”
Los Angeles, CA, USA
January 21, 2021 7:07 PM
“I saw an ad for a blackcass hand held chainsaw. What arrived was only a chain. Never received anything else ”
Ordered Stihl and Dewalt battery operated Chainsaws and only received chains and blades, Waikoloa, HI, USA
Waikoloa, HI, USA
January 22, 2021 11:04 PM
“I ordered and paid for:
2 Stihl Battery operated Chainsaws and 1 Dewalt battery-operated Zigsaw for Christmas gifts. After almost 2 months, I received 2 chains and a couple of zigsaw blades!!!!
Big scam. ”
Walmart, 505 Touring Dr, AUBURN, IN, 46706, USA
January 21, 2021 12:00 PM
“Employees not wearing masks.
Source: Osha.gov | Receipt Date: 2020-10-27 ”
Dairy Queen, 1018 W 7th St, AUBURN, IN, 46706, USA
January 21, 2021 12:00 PM
“Employees are testing positive for Covid-19. Employer not quarantining exposed employees. Employer only allowing time off if employees test positive for Covid-19
Source: Osha.gov | Receipt Date: 2020-12-07 ”
Interior Wood Design, 334 Sacramento Street, AUBURN, CA, 95603, USA
January 14, 2021 12:00 PM
“3203(a)(4)(6): Employer is not enforcing any COVID-19 requirements. Employees and contractors do not wear face mask, no one is required to do temperature checks prior to reporting to work. Common tools are not disinfected. 4184(a): Rover "A" Computer Control Router (CNC) -- was modified and guards w... ere removed but never installed.
Source: Osha.gov | Receipt Date: 2020-11-17 ”
FRED MEYER STORES INC, 801 Auburn Way N, AUBURN, WA, 98002, USA
January 14, 2021 12:00 PM
“The employer was aware of positive COVID 19 employee illnesses in the store but did not implement additional controls. Other employees were not made aware of possible COVID 19 exposures at the store. Extra sanitizing measures have been inconsistent; regular hourly cleaning is inconsistent due to lac... k of sanitizers and cleaners.
Source: Osha.gov | Receipt Date: 2020-05-05 ”
Recent Interesting Reports
Symptoms: Headache Chills Fatigue Joint Pain Muscle Pain Soreness
Sevierville, TN, USA
January 22, 2021 1:14 PM
“Moderna first vaccine 12/23/20. Arm felt sore a little worse than a tetanus shot. Felt pretty fatigued the next two days afterwards. Second Moderna vaccine 01/20/21. Arm felt sore pretty much within a couple of hours. The next day had hot/cold chills, muscle/joint pain and headache. The 2nd day my... injection site was red/warm to touch and has spread quite a bit. Showed the Covid screeners and they said that this is common after the 2nd shot. Took Tylenol and will continue to watch. ”
January 14, 2021 11:44 AM
“I wonder how many people were duped by this disreputable company! Guess I should know better than to order from a company I know nothing about! Shame on them for taking hard earned money during this day and time. And shame on Facebook for allowing them to advertise. ”
SuperFresh Glen Rock, Lincoln Avenue, Glen Rock, NJ, USA
January 3, 2021 5:22 AM
“I bought 9lives canned cat food and 3 of 4 cans had been expired from 11/11/19. Their store is not offering refunds but if I had not looked at the date my cats would have got sick ”
Goodman, MO, USA
January 8, 2021 12:49 PM
“On December 14, 2020 I ordered the Blackcass battery operated chainsaw. On January 8, 2021 I received a chain with two handles attached. ”
January 23, 2021 5:18 PM
“I lost $240k on Luckin Coffee, all my life savings. Now I'm broke af. I believed luckin was growing strong and becoming the next asia starbucks. I didn't know they could cheat on balance sheet, and had no idea about VIE structure and that a company can just fail in 3 months. From Nov to Jan did a 30... 0% gain. I was just late to the party and entered at the wrong time, and played really badly.... I learned the lesson the hard way and I'm gonna just invest in etfs, gold and bonds for the rest of my hopefully long but quite useless life.
Source: Reddit ”
Indianapolis, IN, USA
January 5, 2021 5:07 PM
“I ordered a Skil handheld battery operated chainsaw and after several weeks received a pocket chainsaw in a small pouch. Never in any of the advertisements for the chainsaw that I ordered were there pictures of the pocket chainsaw I received. I even used PayPal to protect myself. This is clearly a... scam and they need to be held accountable. This was Christmas present for someone and not only was it late, now it's not even what I ordered!! ”
Paroex Chlorhexidine Gluconate Oral Rinse, 4 oz and 16 oz - recalled due to Potential contamination with Burkholderia lata, USA
December 28, 2020 8:00 PM
“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: December 28, 2020
Recall details: Schaumburg, Illinois, Sunstar Americas, I... nc. (SAI) is voluntarily recalling Paroex® Chlorhexidine Gluconate Oral Rinse USP, 0.12% products bearing an expiration date from 12/31/2020 – 9/30/2022 to the consumer level. This product may be contaminated with the bacteria Burkholderia lata. This is an expansion of the recall initially announced on October 27, 2020. 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, 29 adverse events have been reported to SAI related to this recall. Affected patients tested positive for Burkholderia lata infections, typically found in sputum cultures while under treatment for other serious medical conditions. Use of the contaminated product on patients with pre-existing respiratory conditions, including those infected with Covid-19, is particularly unsafe.
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 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 firstname.lastname@example.org 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 follow below:
-Paroex® Chlorhexidine Gluconate Oral Rinse USP, 0.12% Size/ Form: 16 fl.oz. Amber Bottles. NDC #: 052376-021-02. Product Code: 1789P. Lots Recalled: ALL LOTS with expiration date from Dec. 31, 2020 through Sep. 30, 2022
- Paroex® Chlorhexidine Gluconate Oral Rinse USP, 0.12% Size/ Form: 4 fl.oz. Amber Bottles NDC #: 052376-021-04. Product Code: 1788P. Lots Recalled: ALL LOTS with expiration date from Dec. 31, 2020 through Sep. 30, 2022.
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. Complete and submit the report Online Regular Mail or Fax: Download form or call 1- 800-332-1088 to request a reporting form, then complete and return to the address on the pre-addressed form, or submit by fax to 1-800-FDA-0178. Sunstar is committed to delivering safe, fully compliant products of the highest quality and is taking necessary steps to prevent future occurrence of this issue. 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 ”
December 31, 2020 11:24 AM
“Responding to an add on facebook I ordered and paid for a battery powered chainsaw on Dec. 13. I then received a confirmation email. On Dec. 30 I received an envelope the size of a cigarette pack containing a manual chainsaw. Where are the fact checkers when you need them? ”
Blackcass pruner. Only received chain as did many others, apparently. Very deceptive advertising., Edgewater, FL, USA
Edgewater, FL, USA
January 1, 2021 8:08 AM
“Ordered Stihl pruner from Blackcass. 2020 Hot Selling GTA 26 Battery Powered Wood Cutter $29.99. Says style Outdoor Portable Carbon Steel Chain. I assumed this meant the chain was carbon steel. Ad goes on to list what's included. You can view their ads online. Received the chain only. When I contac... ted company, they informed me I had only ordered the chain. Who buys just the chain? I am finding others who are experiencing the same issue. Disputing through PayPal also. Feel this is quite the scam. ”
Fresenius Kabi USA Ketorolac Tromethamine Injection, USP, 30 mg/mL - recalled due to Presence of particulate matter, USA
January 8, 2021 6:01 PM
“Company name: Fresenius Kabi USA
Brand name: Fresenius Kabi
Product recalled: Ketorolac Tromethamine Injection, USP, 30 mg/mL
Reason of the recall: Presence of particulate matter
FDA Recall date: January 08, 2021
Recall details: Fresenius Kabi USA is voluntarily recalling a single lot of Ketoro... lac Tromethamine Injection, USP, 30 mg/mL, 1 mL fill in a 2 mL amber vial to the user level due to the presence of particulate matter. Particulate matter was found in reserve sample vials. No adverse event reports have been received for the recalled lot, which was produced and sold in 2019.
Administration of products containing particulate matter could obstruct blood vessels and result in local irritation of blood vessels, swelling at the site of injection, a mass of tissue that could become inflamed and infected, blood clots traveling to the lung, scarring of the lung tissues, and allergic reactions that could lead to life-threatening consequences.
Ketorolac Tromethamine, a nonsteroidal anti-inflammatory drug, is indicated for the short-term (up to 5 days in adults) management of moderately severe acute pain that requires analgesia at the opioid level. The total combined duration of use of oral Ketorolac Tromethamine and Ketorolac Tromethamine Injection should not exceed 5 days. Listed below is a table of the recalled lot distributed nationwide in the United States to wholesalers, distributors, hospitals, and pharmacies between March 28, 2019 and September 3, 2019.
Product Name/Product size: Ketorolac Tromethamine Injection, USP, 30mg / mL, 1 mL fill in a 2 mL amber vial
NDC Number: 63323-162-01
Product Code: 160201
Batch Number: 6121083
Expiration Date: 02/2021
First Ship Date: 03/28/2019
Last Ship Date: 09/03/2019
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 the affected lot, 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 ”