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Scotts Valley, California, United States
Updated: December 5, 2020 12:00 PM
Bay Photo Lab, 920 Disc Drive, SCOTTS VALLEY, CA, 95066, USA
December 5, 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... e covering by all employees. Title 8 CCR Sections 3203 & 3380
Alleged Hazards: 1, Employees Exposed: 1
Source: Osha.gov | Receipt Date: 2020-11-10 ”
Recent Interesting Reports
Pittsburgh, PA, USA
January 19, 2021 10:19 PM
“My puppy Angus, at age 5 months, ate a small amount of a dream bone on Jan 9, 2020 in the afternoon, and then started crying and pacing, not eating any more. About 5 pm, he refused to eat, and went to lie down in his bed, not begging at our table while we ate. He seemed stiff, and lay down with his... neck stretched out. Soon he was unresponsive and glassy-eyed, and stiff as a board. I took him to the Emergency vet, who did not think that there was any obstruction, and while at the vet's he improved, so I brought him home for observation. The vet said that it could be the onset of a neurological condition, or something in the Dreambone. He recovered, is now 18 months (it is more than a year later) and has never had a similar episode. By a process of elimination, it is probable that the Dreambone caused this reaction, and that it wasn't lethal because he only ate a small amount. ”
Long Island City, Queens, NY, USA
January 14, 2021 8:51 PM
“I am a teacher and am authorized to get the Moderna vaccine. I made an appointment in Ridgewood 2 days ago. Appoint was at 5:20 but didn't get my shot until 7:40. The lines are extremely long at night. But the nurse said they are empty in the morning. Once you get inside it is very fast, everyone is... very helpful and you can sign up for your second vaccine. They make you wait 15 mins to make sure you're ok before you leave. I have no side effects from the shot and feel fine. ”
January 4, 2021 11:00 AM
“Company name: Essaar Inc.
Brand name: Soho Fresh
Product recalled: 70% Rubbing Alcohol
Reason of the recall: Contaminated with Methanol
FDA Recall date: January 04, 2021
Recall details: Company Announcement Essaar Inc. is voluntarily recalling lot 200528303 of Soho Fresh 70% Rubbing Alcohol... in 33.81 oz. clear plastic bottles to the consumer level. FDA analysis of the product revealed it is contaminated with methanol. 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, Essar Inc. has not received any reports of adverse events related to this recall. The product is used as an external purpose use rubbing alcohol and is packaged in 33.81 oz. clear plastic bottles with lot number 200528303 and UPC 7502268987367.
Soho Fresh was distributed nationwide to retail stores. Essaar Inc. is notifying its distributors and customers by email and mail and is arranging for the return of all recalled product to Essaar Inc. Consumers that have product which is being recalled should stop using and discard or return to place of purchase or to Essaar Inc. contacting via email or phone or mailing address mentioned above for arrangements of return. Consumers who have purchased this product should not open the package or use the contents. Instead, they should return the product to the location of purchase for a full refund or call Essaar Inc. at 201-647-7606 Monday to Friday 9am to 5pm, Eastern Standard Time. Essaar Inc. can also be reached via email at email@example.com.
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. 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
This recall is being conducted with the knowledge of the U.S. Food and Drug Administration. FDA’s update
Check the full recall details on fda.gov
Source: FDA ”
Orlando, FL, USA
January 4, 2021 10:32 PM
“Totally false advertising. I order two chainsaws and got two open 26" chains with straps on both ends. Not happy. This advertising was misleading and took over 30 days to receive this product in the mail. I am totally dissatisfied with this purchase and company. ”
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 ”
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!! ”
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. ”
Tracy, CA, USA
January 21, 2021 4:42 PM
“I fed both my dogs a chicken wrapped dream ”
January 23, 2021 3:32 PM
“Luckin Coffee is a coffee retailer founded in 2017 based in Xiamen, the People’s Republic of China. Luckin Coffee owns and operates stores selling food and beverages, as well as a mobile application for food and beverage purchases.
On May 17, 2019, Luckin Coffee conducted an Initial Public Offer... ing (“IPO”) of its ADSs.
On January 31, 2020, Muddy Waters Research published a report stating that Luckin Coffee had fabricated portions of its financial statements beginning in the third quarter of 2019, citing “smoking gun evidence” such as thousands of hours of store video, customer receipts, and monitoring of the Company’s mobile application data. On this news, the price of Luckin Coffee ADSs fell from $36.40 per share on January 30, 2020, to $32.49 per share on January 31, 2020.
On February 3, 2020, Luckin issued a press release denying Muddy Waters’s allegations. The Company “categorically denie[d] all allegations in the [Muddy Waters] Report” and assured investors that the “methodology of the Report is flawed, the evidence is unsubstantiated, and the allegations are unsupported speculations and malicious interpretations of events.”
On April 2, 2020, contrary to its previous denials, Luckin Coffee disclosed that it had conducted an internal investigation and had found that Luckin Coffee’s Chief Operating Officer Jian Liu and several of his direct reports had fabricated over $300 million of sales beginning in the second quarter of 2019. On this news, the price of Luckin Coffee ADSs fell from $26.20 per share on April 1, 2020 to $6.40 per share on April 2, 2020 – a decline of over 75%.
Luckin Coffee ADSs have now been delisted from trading on the NASDAQ. ”
January 17, 2021 11:59 PM
“The FSA announced the recall of several dog food products by Mars Petcare UK because they may contain high levels of vitamin D which exceed the maximum permitted intake.
FSA advises pet owners that if they have bought any of the following dog food products, you should stop feeding them to your do... g and contact Mars Petcare Customer Service at 0800 013 3131. If you have concerns that your pet may be showing symptoms of illness after eating one of the affected products, please contact a veterinarian.
- CHAPPIE Complete Chicken & Wholegrain Dry Dog Food (3kg). Batch code: 045F9MIN05. Best before: 44692
- PEDIGREE Mixer Adult Dry Dog Original (3kg). Batch code: 046E9MIN05 | 046F9MIN05 | 048A9MIN05. Best before: 12 February 2022 | 20 February 2022 | 22 February 2022
- PEDIGREE Mixer Adult Dry Dog Food Original (10kg). Batch code: 046E9MIN08 | 047C9MIN08. Best before: 12 February 2022 | 17 February 2022
- PEDIGREE Adult Complete Dry Dog Food with Chicken & Vegetables (12kg). Batch code: 046C9MIN08 | 046D9MIN08 | 046E9MIN08. Best before: 10 February 2022 | 11 February 2022 | 12 February 2022
- PEDIGREE Adult Complete Dry Dog Food with Chicken & Vegetables (2.6kg). Batch code: 045F9MIN05 | 047A9MIN05. Best before: 06 February 2022 | 15 February 2022
High levels of vitamin D fed to a pet over a short period (weeks/months) should not cause undue concern. Over a longer period of feeding, ingestion of elevated levels can lead to potential dog health issues. Vitamin D, when consumed at very high levels, can lead to serious health issues in dogs including renal dysfunction.
Check the full recall details on the FSA website food.gov.uk
Source: FSA ”