Create a Report
Please provide report title
Please provide location
Please provide details
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.
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.

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

McDonald's, 481 Hyde Park Rd, Leechburg, PA 15656, USA

Latest report: April 16, 2020 12:00 PM
#coronaviruscovid19 #481hydeparkroad #leechburg #pennsylvania #unitedstates
HZ

McDonald’s Closes After Worker Tests Positive for COVID-19

2 years ago

A McDonald’s in Westmoreland County is temporarily closed after a worker tested positive for coronavirus. The worker is now self-quarantining.

Source: pittsburgh.cbslocal.com See Less
364


Related Reports

Multiple employees(3) at WALGREENS in RIO RANCHO, NM tested positive for Covid-19 and the company is on the Rapid Response COVID-19 Watchlist Event Date: 08/15/2022,

Source: env.nm.gov See Less
487


Multiple employees(2) at WALGREENS in LAS CRUCES, NM tested positive for Covid-19 and the company is on the Rapid Response COVID-19 Watchlist Event Date: 08/15/2022,

Source: env.nm.gov See Less
145


An employee(1) at WALMART NEIGHBORHOOD MARKET in LAS CRUCES, NM tested positive for Covid-19 and the company is on the Rapid Response COVID-19 Watchlist Event Date: 08/15/2022,

Source: env.nm.gov See Less
145


Multiple employees(4) at WALMART SUPERCENTER in LOS LUNAS, NM tested positive for Covid-19 and the company is on the Rapid Response COVID-19 Watchlist Event Date: 08/15/2022,

Source: env.nm.gov See Less
487


Multiple employees(2) at WALMART SUPERCENTER in ALBUQUERQUE, NM tested positive for Covid-19 and the company is on the Rapid Response COVID-19 Watchlist Event Date: 08/15/2022,

Source: env.nm.gov See Less
487


Multiple employees(2) at WHATABURGER in LAS CRUCES, NM tested positive for Covid-19 and the company is on the Rapid Response COVID-19 Watchlist Event Date: 08/15/2022,

Source: env.nm.gov See Less
145


It looks they are all hitting expiry, packets i had in the house, and have seen while shopping. Not sure if it means that they will be less reliable, or not work at all. Either way, not good timing heading into fall, where covid may flare up again. See Less
7.1K


Went to take COVID rapid test that were mailed out to our house by the government. Noted expiration date. The test was expired. Unable to use See Less
246


MA
M.......7
Would never use EVER
Reply 2 weeks ago
I got this covid booster, and flu shot at the same time. Zero side effects so far, and I am on day 3 now. I assume by now I am in the clear. The picture says moderna, but he assured me it was the pfizer. See Less
1.7K


1) In the basement, the unfinished remolding has exposed the underground lifted pipes and when it rains the floor floods. There is black mold growing in the basement and smells of mildew. Employees are experiencing nasal irritation and headaches. 2) The basement has never been cleaned nor... See More has the remolding been completed. 3) The employer is not following CDC's Interim Guidance for Businesses and Employers Responding to Coronavirus Disease 2019. Employees are not wearing facial coverings or practicing social distancing. 4) There are no barriers between the employee and customers to reduce the exposure of COVID-19.

Alleged Hazards: 4, Employees Exposed: 5
Source: Osha.gov | Receipt Date: 2021-08-11
See Less
364


Recent Interesting Reports

I received an order I had placed and paid for the product as well as postage that had a fraudulent postage label and was I required to pay an additional $4.80 to accept the package. See Less
2.1K


Salon Technologies International. Inc. is voluntarily recalling one lot of Antica Ocean Citron Hand Sanitizer (alcohol) Gel 65%, Lot 1166A. Expiration 6/18/2023 to the consumer level. Firm lab testing has found the product to contain benzene. Benzene is classified as a human carcinogen. Exposure to benzene can... See More 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 which can be life-threatening.

Salon Tech International, Inc. has not received any reports of adverse events related to this recall. The product is used to help reduce bacteria, that potentially can cause disease, when soap and water are not available. 512 bottles of Antica Ocean Citron Hand Sanitizer (alcohol) Gel 65%, Lot 1166A, Expiration 6/18/2023 was distributed in the Seattle, Washington area.

Salon Technologies International. Inc. has notified its distributors by email and is arranging for return of all recalled products. Consumers that have product which is being recalled should stop using and return unused product to where it was obtained.

In case you experienced 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.

Company name: Salon Technologies International Inc.
Brand name: Antica Farmacista
Product recalled: Ocean Citron Hand Sanitizer
Reason of the recall: Product contains benzene
FDA Recall date: September 19, 2022

Source: fda.gov
See Less
1.6K


Family Dollar is initiating a voluntary retail level product recall of certain products regulated by the U.S. Food and Drug Administration (FDA) that were stored and inadvertently shipped to certain stores on or around May 1, 2022 through June 10, 2022 due to product being stored outside... See More of labeled temperature requirements.  This notice covers the recall of Over-the-Counter Medical Devices. An earlier notice issued July 21, 2022 covered a related recall of Over-the-Counter Pharmaceutical Products. To date, Family Dollar has not received any consumer complaints or reports of illness related to this recall.  This recall is being conducted out of an abundance of caution.

- Recalled products:

900260 900260 CLEARBLUE SMART COUNTDOWN PRGNCY TST 1CT
900794 900794 LS SKYN NON LATEX LUBRICATED CONDOM 3CT
901260 901260 VERIQUICK PREGNANCY TEST 1CT
902343 902343 FIRST RESPONSE 2 CT
903409 903409 SKYN ORIGINAL NON LATEX CONDOM 12CT
903415 903415 SKYN ELITE NON LATEX CONDOM 12CT
939504 939504 VERIQUICK PREGNANCY TEST 1 CT
900752 900752 AT HOME MARIJUANA TEST STRIP
902816 902816 TROJAN ULTRA RIBBED LUBED 3CT
903756 903756 VERIQUICK PREGNANCY TEST 2 CT
999763 999763 TROJAN ULTRA THIN CONDOM LATEX 3CT
998221 998221 SKYN ELITE LARGE NON LATEX CONDOM 12CT
998869 998869 PREFERRED UTI TEST 1 CT
900265 900265 LIFESTYLES ULTRA SENSITIVE CONDOMS 12CT
900531 900531 CLEAR EYES CONTCT LENS DRPS LBRCTNG .5FO
999009 999009 B L BIOTRU MULTI PURPOSE SOLUTION 4 FLOZ
902274 902274 GS SALINE SOLUTION 12FL OZ
901443 901443 KY JELLY LUBRICANT 2 FL OZ
901960 901960 OPTI FREE REPLENISH MULTI PURPOSE 2 OZ
999801 999801 SIMPLY SALINE NASAL MIST 3.1 OZ
900457 OPTI FREE PURE MST DSINFCTNG SLTN 4FL OZ
902139 902139 DENTEMP ONE STEP .077OZ
906018 906018 FIXODENT ORG CREAM 2.4OZ
998762 998762 DRTALBOT TDDLR TTHPSTE BRSH TUTTI FRUTTI
905076 905076 CURAD STRNG WATRPRF STRIP 1IN 20CT
906312 906312 GS DENTURE CLEANSER GRN TAB 40CT
999619 999619 FIXODENT ADH CREAM ULTRA MAX HOLD 2.2OZ
999037 999037 CURAD FIRST AID KIT
903377 903377 POLIGRIP POWER MAX HOLD 2.2OZ
999417 999417 NEW SKIN LIQUID BANDAGE CLEAR .3FL OZ
900737 900737 TRVL KIT TOTHBRSH CAP PASTE IN POUCH 1CT
901239 901239 FIXODENT ORG CREAM TRAVEL .75OZ
906131 906131 POLIDENT DENTURE CLNS TAB 28CT
900334 900334 POLIGRIP ADH CREAM FREE 2.4OZ
906023 906023 GS DENTURE CLEAN OVRNT TAB 40CT
901634 901634 POLIDENT DENTURE CLEANSERS 84 CT
901777 901777 POLIDENT OVERNIGHT WHITENING TAB 28CT
906402 906402 FIXODENT ADH CREAM WITH SCOPE 2OZ
999632 999632 POLIGRIP EXTRACARE ADHESIVE CREAM 2.2OZ
900085 900085 SUPER POLIGRIP ADH CREAM .75OZ
900723 900723 POLIGRIP DENTURE ADHESIVE ORIGINAL 2.4OZ

This recall goes to the retail store level. Not all of the products listed were sent to all stores. Family Dollar has notified its affected stores asking them to check their stock immediately and to quarantine and discontinue the sale of any affected product. Customers that may have bought affected product may return such product to the Family Dollar store where they were purchased without receipt. 

This recall does not apply to Connecticut, Maine, Massachusetts, New Hampshire, Rhode Island, Vermont, Washington, Alaska, or Hawaii as Family Dollar does not have any stores in Alaska or Hawaii and no Family Dollar stores in any of the other states received any products subject to this recall. Customers should contact their physician or health care provider if they have experienced any problems that may be related to using these products.

Company name: Family Dollar
Brand name: Multiple brand names
Product recalled: Various OTC medical products
Reason of the recall: Product was stored outside of labeled temperature requirements.
FDA Recall date: September 16, 2022

Source: fda.gov
See Less
463


She began to have diarrhea 3 days ago after eating the first Dream bone. We didn't relate the problem. She got a second one the next day and the diarrhea continued for 3 days. Last night blood began to pour from her. Today they are trying to see where the bleeding is coming from to save her. | Symptoms: Diarrhea, Bloody Stool See Less
300


This package was delivered addresses to me, I didn’t order it but it came from an online seller at 1555 N. Chrisman Riad in Tracy, CA 95304 See Less
811


On 21 Sept we drove up to the Kirtland gate to enter Hanscom. My spouse needed to renew her dependent ID Card and was denied base access. We had to go enter the base at the Vandenberg gate to get her a base pass.(Strange Rule me being... See More a retired vet with a valid ID not being able to vouch for her). While at the Pass building my wife took a fall and injured her right arm and right leg causing a laceration and burses. No hand rail was present on the two steps at the pass office building. and the officers in the building only offered her a chair. She was bleeding from her arm so after receiving a pass I bandaged her from my first aid kit in our car.
Why wasn't there a hand rail at the steps and why was no first aid offered?
See Less
2.2K


East Windsor, New Jersey, Eugia US LLC (formerly AuroMedics Pharma LLC) has initiated a voluntary recall of lot number AC22006 of AuroMedics Acyclovir Sodium Injection 500 mg per 10 mL (50 mg/mL), 10 mL single dose vial to the consumer level from the U.S. market due to... See More a product complaint for the presence of a dark red, brown and black particulate inside the vial.

Risk Statement: The administration of an intravenous product containing particulates has the potential to result in inflammation, allergic reactions, or circulatory system complications which could be life-threatening. To date, Eugia US LLC has not received reports of any adverse events or identifiable safety concerns attributed to the product consumed for this lot.

AuroMedics Acyclovir Sodium Injection 500 mg per 10 mL (50 mg/mL), contains acyclovir, a synthetic nucleoside analog, active against herpes viruses. Acyclovir Sodium Injection is indicated for the treatment of initial and recurrent mucosal and cutaneous herpes simplex (HSV- 1 and HSV-2) in immunocompromised patients and initial clinical episodes of herpes genitalis in immuno-competent patients. It is packaged in a glass vial labeled with NDC 55150-154-10. The lot being recalled is AC22006 with an expiration date of 08/2023. Eugia US LLC shipped the entire lot to wholesalers nationwide from June 8, 2022, through June 13, 2022.

The product label is as shown below: Eugia US LLC is notifying its direct consignees by recall letters and is arranging for return/ replacement of all recalled products. Wholesale customers and health professionals that have the product lot which is being recalled should immediately place the recalled lot on hold.

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. This recall is being conducted with the knowledge of the U.S. Food and Drug Administration.  

In case you experienced 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.

Company name: Eugia US LLC
Brand name: Auromedics
Product recalled: Acyclovir Intravenous Product
Reason of the recall: Presence of a dark red, brown and black particulate inside the vial
FDA Recall date: September 27, 2022

Source: fda.gov
See Less
463


The package was empty inside. It contained simply bubble wrap on bothe sides, but no contents or paper. I just came home and opened my mailbox received my electric bill a couple of standard Flyers and this manila envelope from an online seller. I was not expecting... See More any packages and I have not ordered any packages. Due to my nervous nature as it is I got outside and ripped the top of the package open and held it away from my face and pinched it open to see no contents inside just the simple bubble wrap that is on the inside of the envelope. I left it outside and I'm about to dispose of it in the trash receptacle. I'm in Crawfordville, FL, USA See Less
3.0K


GA
anonymous7079
Us too
Reply 1 day ago
L8
anonymous7082
Received one today from same.
Reply 1 day ago
My sender sent it back there & I don’t know how to get in contact with the sender. See Less
7.1K


Last 30 days