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Domino's Pizza Fairfield Victoria, 306 Station St, Fairfield VIC 3078, Australia

Total all time reports:  1
Latest report: May 17, 2020 12:00 PM
#coronaviruscovid19 #dominospizza #306stationstreet #fairfield #victoria #australia
JV

Store closed due to possible COVID-19 exposure

1 year ago

A Domino’s restaurant in Melbourne’s north is currently closed for 2 weeks after possible exposure to COVID-19.

Source: news.com.au See Less
266


Related Reports

A power outage Wednesday morning in central and west Fairfield left nearly 2,835 homes and businesses in the dark, with another 100 customers without power in Vacaville.
The largest outage in Fairfield was reported shortly after 9 a.m.
An outage that affected 25 businesses along the west... See More side of Oliver Road was reported at approximately 9:05 a.m. Power was restored there about 90 minutes later.

Source: dailyrepublic.com
Source publication date: 2021 10 20
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1. Employees are suffering from musculoskeletal disorders due to loading and unloading blood collection equipment from the trucks and also with assisting patients on and off the tables. 2. Employees have not received adequate ergonomic training. 3. Employees utilized chemical to clean equipment and patient collection tables... See More have not received adequate training. 4. Employees have received needle sticks from equipment used in blood draws. 5. Employer has not performed a hazard assessment for employee exposed to patient to determine COVID exposure. 6. Employer has not provided proper PPE and training to employee for COVID exposure. 7. Employer is not properly recording COVID illness in the OSHA 300 logs. 8. Employee is not following CDC guidelines related to COVID precautions such as not being able to socially distance and are working in unventilated indoor spaces. 9. Employees are not being notified when they are exposed to donors/coworkers under investigation for COVID. 10. Employer is not ensuring that contracted cleaning services are properly disinfecting the worksites per the CDC guidelines.


Source: Osha.gov | Receipt Date: 2021-02-05
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1. The employer did not ensure to conduct a workplace-specific identification of all areas, interactions and activities that could potentially expose employees to COVID-19 hazards. T8 CCR 3205(c)(2)(D). 2. The employer did not ensure that unvaccinated employees are furnished with respirators upon employee requests in accordance with... See More section 5144(c)(2). T8 CCR 3205(c)(7)(D)(2).

Alleged Hazards: 2, Employees Exposed: 1
Source: Osha.gov | Receipt Date: 2021-07-13
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1) Employees are not quarantining after exposure to COVID-19. On or about 07/19/2021, a classroom was sent home due to a positive COVID-19 case however the employees exposed were not quarantining. 2) Students are allowed to enter the school with symptoms of COVID-19 exposing employees to the... See More disease. 3) Social distancing among employees and students is not maintained.

Alleged Hazards: 3, Employees Exposed: 2
Source: Osha.gov | Receipt Date: 2021-07-22
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The employer did not ensure to exclude unvaccinated employees who were exposed to a COVID-19 case from the workplace until the requirements of subsection (c)(10) are met. T8 CCR 3205(c)(9)(B).

Alleged Hazards: 1, Employees Exposed: 1
Source: Osha.gov | Receipt Date: 2021-08-03 See Less
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1. The employer did not ensure to clean and disinfect areas, materials and equipment used indoors by a COVID-19 case if the area is to be used by another employee within 24 hours. T8 CCR 3205(c)(7)(B)(2). 2. The employer did not ensure to make COVID-19 testing available... See More to employees in the exposed workgroup immediately upon being covered by this section. T8 CCR 3205.1(c)(2)(A). 3. The employer did not ensure that employees in the exposed workgroup wear facial coverings when indoors, outdoors and when closer than 6 feet from other persons. T8 CCR 3205.1(d)(1). 4. The employer did not ensure to exclude unvaccinated employees who were exposed to a COVID-919 case from the workplace until the requirements of subsection (c)(10) are met. T8 CCR 3205(c)(9)(B). 5. The employer did not ensure that facial coverings were provided and worn by all unvaccinated employees at the Fairfield store location. T8 CCR 3205(c)(6)(A). 6. The employer did not ensure that employees who were exposed to a known COVID-19 case during the high-risk exposure period were given notification of the exposure within one business day. T8 CCR 3205(c)(3)(3).

Alleged Hazards: 6, Employees Exposed: 1
Source: Osha.gov | Receipt Date: 2021-07-29
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The employer did not give an effective COVID-19 prevention program in that the employer did not ensure that COVID-19 precautions per the state executive and local public health department orders are being followed at the workplace in the following instances: 1. the employer did not give notice... See More within one business day of potential COVID-19 exposure to all employees who may have had COVID-19 exposure. 2. The employer did not implement cleaning of areas, material and equipment used by a COVID-19 case during the high-risk exposure period and disinfection if the area, material or equipment is indoors and will be used by another employee within 24 hours of the COVID-19 case. T8 CCR 3205(c)(7)(B)(2).

Alleged Hazards: 2, Employees Exposed: 1
Source: Osha.gov | Receipt Date: 2021-07-23
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Employees are not provided with personal protective equipment such as gloves and masks. Cleaning products for disinfecting are not provided by the employer.

Alleged Hazards: 2, Employees Exposed: 10
Source: Osha.gov | Receipt Date: 2021-04-02 See Less
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The employer did not maintain an effective COVID-19 prevention program in that the employer did not ensure that COVID-19 precautions per the state executive and local public health department orders are being followed at the workplace in the following instances: 1. The employer did not ensure personal... See More identifying information of COVID-19 cases or persons with COVID-19 symptoms shall be kept confidential. T8 CCR 3205(c)(3)(C). 2. The employer did not provide face coverings and ensure they are worn by employees. T8 CCR 3205(c)(7)(A). 3. The employer did not ensure that COVID-19 cases are excluded from the workplace until the return to work requirements of subsection (c)(11) are met. T8 CCR 3205(c)(10)(A).

Alleged Hazards: 3, Employees Exposed: 1
Source: Osha.gov | Receipt Date: 2021-03-18
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A deep cleaning was not conducted following worker's testing positive for COVID-19. After workers tested positive for COVID-19 and stayed home for two weeks, one employee re-tested positive and continues to see patients in the office.

Alleged Hazards: 1, Employees Exposed: 15
Source: Osha.gov | Receipt Date:... See More 2021-02-09 See Less
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Recent Interesting Reports

Shipment was supposed to arrive Friday.  Now I received the following message : Your shipment has potentially been delayed due to emergency or other conditions at 6:46 pm on October 17, 2021. | Symptoms: Other See Less
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GR
Grinsler
Same here. Mine arrived at Teterboro 10/14 @ 3:35 pm. 10/17 update says "Processing Exception, Other Delay Your shipment has potentially been delayed due to emergency or other conditions at 6:50 pm on October 17, 2021."
Reply 1 week ago
MI
Mitch
Same very important documents are there What the hell is going on
Reply 5 days ago
Over recent weeks, SafelyHQ received a surge of reports from our community citing lost and delayed packages from the US Postal Service specifically citing packages that routed through Teterboro NJ Distribution Center. The New York Post - which follows and identifies signals from our community followed up... See More on our story and reported on it yesterday.

If you have any health, safety, or community issue, including issues with delivery services, report it to SafelyHQ. Reporting will help identify and bring attention to common problems that impact friends, family, and our communities at the local and national level.

Read the full NY Post story here: nypost.com
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98


Company name: Eli Lilly and Company
Brand name: Lilly
Product recalled: Glucagon Emergency Kit
Reason of the recall: Loss of potency
FDA Recall date: September 26, 2021
Recall details: Eli Lilly and Company (NYSE: LLY) is voluntarily recalling lot D239382D, Expiration April 2022, of Glucagon Emergency Kit... See More for Low Blood Sugar (Glucagon for Injection, 1 mg per vial; Diluent for Glucagon, 1 mL syringe), to the consumer/user level. Lilly is recalling lot D239382D to the patient level because of a product complaint reporting that the vial of Glucagon was in liquid form instead of the powder form.

The firm’s investigation indicates that the liquid in this Glucagon vial could be related to the manufacturing process. The use of the liquid form of this product may fail to treat severe low blood sugar due to loss of potency.

Risk Statement: Severe hypoglycemia in patients with diabetes, if not reversed, can potentially cause adverse health consequences ranging from transient, minor complaints to neurological damage, seizures, and even death if not promptly treated. Associated with the one product complaint, it was reported to Lilly that the involved patient experienced lack of drug effect and also reported subsequent seizures.

Glucagon Emergency Kit is used as an anti-hypoglycemic agent and a gastrointestinal motility inhibitor indicated for the treatment of severe hypoglycemia in pediatric and adult patients with diabetes mellitus. The product is packaged in a kit containing 1mg of freeze-dried (lyophilized) product in a 3 mL vial and a pre-filled diluent syringe. The affected Glucagon Emergency Kit lot is D239382D and the expiration date is April 2022 (label expiry date: 04 2022). The lot number can be found on the label of the kit as well as the vial (refer to the photos provided below – Appendix A). The lot was distributed nationwide to wholesalers and retailers.

Wholesalers and Distributors with an existing inventory of Glucagon Emergency Kit lot D239382D should cease distribution and quarantine the product immediately.

Instructions for Wholesalers and Pharmacists: If you have distributed the recalled product, please notify any accounts or additional locations which may have received product from the recalled lot from you. Please conduct a sub-recall to those accounts and communicate this recall information immediately.

Instructions for Consumers: Consumers in possession of Glucagon Emergency Kit lot D239382D should contact The Lilly Answers Center at 1-800-545-5979 for return and replacement instructions for the product (hours of operation are Monday- Friday, 9AM – 7PM EST) and should contact their health care provider for guidance. Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to taking or using this 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.

This recall is being conducted with the knowledge of the U.S. Food and Drug Administration. APPENDIX A The Lot Number is found on the kit and vial labels as can be seen in the example label below. 

Check the full recall details on fda.gov

Source: FDA
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I mailed out a Shutterfly book to my cousin in Fl, from where I live in NY on July 1st and the last known tracking of it was 4 days later in aTeterboro, NJ. It’s a bright orange package, you can’t miss! As of today Oct. 15th,... See More it’s still missing. In mid Sept. Shutterfly was nice enough to print a second book, which I had sent direct from Shutterfly to Fl. My cousin never got that book either. After contacting Shutterfly again, they were kind enough to send out a 3rd book, which she finally got. For the first package, I sent out, I put in a missing claim with USPS and continue to get emails saying they are still working on finding my missing package. What a joke. See Less
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Company name: Bryant Ranch Prepack
Brand name: Bryant Ranch Prepack
Product recalled: Methocarbamol 500mg
Reason of the recall: Bottles labeled as Methocarbamol 500mg tablets were found to contain Methocarbamol 750mg tablets.
FDA Recall date: October 19, 2021
Recall details: Burbank, CA, Bryant Ranch Prepack is voluntarily recalling... See More 1 lot of Methocarbamol 500mg, Tablets to the consumer level. The bottles labeled as Methocarbamol 500mg Tablets have been found to contain Methocarbamol 750mg Tablets.

Risk Statement: If a patient takes a 750mg Tablet of Methocarbamol instead of the prescribed 500mg Tablets, it potentially could result in Excessive Central Nervous System depression which may result in nausea, sedation, fainting, falls, seizure, coma, and death. Bryant Ranch Prepack has not received any reports of adverse events related to this recall.

The product is used together with rest, physical therapy, and other measures for the relief of discomfort associated with acute, painful musculoskeletal conditions and is packaged in a white round bottle with a red and white label, which reads Methocarbamol 500mg packaged in counts of 30 (NDC:7133517952), 60 (NDC: 7133517954), and 90 (NDC:7133517957) pills. The affected Methocarbamol 500mg lots include the following Lot Number 163935/ Exp. Date 10/22. The product can be identified by red and white label with a yellow border at the top and bottom of the label, top of the label reads “Packaged by Bryant Ranch Prepack”, labels are pictured below. The Methocarbamol 500mg was distributed Nationwide to multiple physician offices.

Bryant Ranch Prepack is notifying its distributors and customers by letter and email and is arranging for return of all recalled products. Consumers that have the bottles labeled as Methocarbamol 500mg Tablets which is being recalled should stop using immediately and return to place of purchase and/or contact their physician. Distributors/Physicians should stop distribution and contact Bryant Ranch Prepack to return the product immediately.

Check the full recall details on fda.gov

Source: FDA
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97


I ordered a hand held battery powered mini chainsaw  in March this year but haven’t received it as yet but I got a wire cutting which is useless and I want my money returned as I think I have been very patient but nearly 6 months is... See More plenty of time to honor.

I have a copy of my receipt and confirmation and I also am sorry that this has been happening to other people  | Symptoms: Other
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I was a premium TokyoTreat subscriber for 6 months, 35$/month, I got only 2 boxes, first when I subscribed, last one after I unsubscribed. Looks like real scam to me, they steal my money See Less
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Bayer is voluntarily recalling all unexpired Lotrimin® AF and Tinactin® spray products with lot numbers beginning with TN, CV, or NAA, distributed between September 2018 to September 2021, to the consumer level due to the presence of benzene in some samples of the products. To date, Bayer... See More has no known reports of adverse events related to this recall.

Benzene is not an ingredient in any of Bayer Consumer Health products. It is important to note that Bayer’s decision to voluntarily recall these products is a precautionary measure and that the levels detected are not expected to cause adverse health consequences in consumers.

Benzene is classified as a human carcinogen. Exposure to benzene can occur by inhalation, orally, and through the skin. Depending on duration and level of exposure, it can result in cancers including leukemia, and blood cancer of the bone marrow, and blood disorders that can be life-threatening. Benzene is found in the environment from natural sources and human activity. Humans around the world are exposed to it from multiple sources and pathways, including inhalation, through the skin, and orally.

The affected Lotrimin® and Tinactin® spray products are over-the-counter antifungal products, sold individually or in combo packs.

The impacted products are:
- Lotrimin® Anti-Fungal (AF) Athlete's Foot Powder Spray
- Lotrimin® Anti-Fungal Jock Itch (AFJI) Athlete's Foot Powder Spray
- Lotrimin® Anti-Fungal (AF) Athlete’s Foot Deodorant Powder Spray
- Lotrimin® AF Athlete's Foot Liquid Spray
- Lotrimin® AF Athlete’s Foot Daily Prevention Deodorant Powder Spray
- Tinactin® Jock Itch (JI) Powder Spray
- Tinactin® Athlete’s Foot Deodorant Powder Spray
- Tinactin® Athlete’s Foot Powder Spray
- Tinactin® Athlete’s Foot Liquid Spray

Product images and information on which lot numbers fall under this recall are available at the link below. There are no issues of concern with Lotrimin®/Tinactin® creams, including Lotrimin® Ultra, or any other Bayer products.

The recalled products are all packaged in aerosol spray cans. The products were distributed in the U.S., Puerto Rico, Canada, and Mexico through a variety of retail channels.

Bayer is also notifying its distributors and retailers by letter and is arranging for returns of all voluntarily recalled products. Consumers who have the products that are being recalled should stop using them.

Check the full recall details on fda.gov

Company name: Bayer U.S. LLC
Brand name: Lotrimin® AF and Tinactin®
Product recalled: Over the Counter (OTC) antifungal spray products
Reason of the recall: Presence of benzene
FDA Recall date: October 01, 2021

Source: FDA
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1 Share


USPS lost yet another package at their Teterboro distribution center, reporting "Processing Exception Delay" with no way to know if it will be resolved or not. See Less
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