Graybar Electric Supply, Mount Vernon Avenue, Pomona, CA, USA
Latest report:
An employee tested positive for coronavirus
3 years ago •reported by user-rrmff754
Graybar in Pomona Ca had an employee test positive for corona Virus. Employer didn't inform staff till there shift was over. Staff was inform to come back to work the next day at 4am. When staff returned there was no sign of cleaning or sanitizing. They did
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not sanitize facility properly. Still left empty cups, soda cans, and trash was full at the employees desk whom tested positive for Covid
1.1K
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Covid cases in my area are high, Rolla, MO, USA
4 months ago •reported by user-cvttz511
Covid number are spiking in the area, especially in the FedEx and UPS terminal, Missouri S&T and Rolla public school's.
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costco optical lab employees are using and selling drugs in the lab
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Papa johns is not protecting their employees from COVID, Papa Johns Pizza, 9123 N Loop 1604 W, San Antonio, TX 78249, United States
8 months ago •reported by user-xwnh6111
Papa johns is not protecting their employees from COVID. I just got COVID and strep tested and it came back positive for both. They immediately told me to come back to work. This is completely unsanitary and unsafe for employees and customers. They are not following protocols
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due COVID -19 and are disregarding everything just to have the correct amount of staffing.
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Possible COVID-19 Symptoms, Cook Out, West Cumberland Street, Dunn, NC, USA
1 year ago •reported by user-rdqk1975
I started feeling symptoms yesterday morning after eating at this location in Dunn. The location was very dirty and none of the people wore masks. I have had to cancel my driver's test, dentist appointment, doctor's appointment and several other events.
| Symptoms: Other
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Lockport CARES, Lockport CARES, Inc, Genesee Street, Lockport, NY, USA
1 year ago •reported by user-fmqy4141
I was staying at a shelter in Lockport Cares and there was a Christian pastor at the shelter. Guess again. I dialed an ubulanxe to go to the hospital because my teeth were bleeding.and I was coughing up blood. The woman told me I should not stay
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at Lockport Cares because I called an ambulance to go to the hospital.
I assume Lockport cares is possibly food poisoning people. Lockport cares gives you bag lunches , breakfast and dinner.
For 2 nights there is always corn or brownies during Bible study at 8pm at night.
I'm not allowed back because I claaid they were food poisoning people
I told the police when I dialed the ambulance.
My blood sugar was low and I was coughing up blood and my teeth were bleeding.
Warning. Lockport Cares does food poisoning
Also there is a hazard for COVID 19. The manager allows COVID 19 positive to stay there without mandatory mask
You are not required to wear mask indoors.amd of you are positive for covid 19, you are not required to wear a mask. There is a woman positive for covid 10 not wearing a mask everyday spreading her disease. Lockport Cares allows kids and married couples to stay the night also.
Lockport cares should be shut down for biohazard. Covid positive wear no masks. A mask is not required for covid positive people.
Warning. | Symptoms: Cough
I assume Lockport cares is possibly food poisoning people. Lockport cares gives you bag lunches , breakfast and dinner.
For 2 nights there is always corn or brownies during Bible study at 8pm at night.
I'm not allowed back because I claaid they were food poisoning people
I told the police when I dialed the ambulance.
My blood sugar was low and I was coughing up blood and my teeth were bleeding.
Warning. Lockport Cares does food poisoning
Also there is a hazard for COVID 19. The manager allows COVID 19 positive to stay there without mandatory mask
You are not required to wear mask indoors.amd of you are positive for covid 19, you are not required to wear a mask. There is a woman positive for covid 10 not wearing a mask everyday spreading her disease. Lockport Cares allows kids and married couples to stay the night also.
Lockport cares should be shut down for biohazard. Covid positive wear no masks. A mask is not required for covid positive people.
Warning. | Symptoms: Cough
36
Detect, Inc. Over the counter Covid-19 Test - recalled due to may give false negative results, USA
1 year ago •source www.fda.gov
Recall notice
Detect, Inc. is voluntarily recalling specific lots of the Detect Covid-19 Test™, their molecular, over-the-counter test used to identify SARS-CoV-2 (the virus that causes Covid-19) in self-collected nasal swabs. The recall affects a total of 11,102 tests shipped to customers from July 26th, 2022 through August 26th,
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2022. The test was granted Emergency Use Authorization (EUA) from the U.S. Food and Drug Administration (FDA) on October 28, 2021. To date, Detect has not received any reports of false negative results related to the affected lots and is issuing this recall out of an abundance of caution.
There is an increased chance that the tests from the lot numbers listed below may give false negative results. Detect has conducted a thorough investigation to identify this issue and has made the decision to conduct a voluntary recall for these lots. The reliability of positive test results is not affected.
Below is a list of the affected lots. The lot number can be found on the side of each test box along with the Use By date.
Lot Number: HB264, Use By Date: 1/1/2023, Number of Tests Shipped: 7,382
Lot Number: HY263, Use By Date: 1/1/2023, Number of Tests Shipped: 1,800
Lot Number: HY264, Use By Date: 1/1/2023, Number of Tests Shipped: 1,920
There is an increased chance that the tests from the lot numbers listed below may give false negative results. Detect has conducted a thorough investigation to identify this issue and has made the decision to conduct a voluntary recall for these lots. To date, Detect has not received any reports of false negative results related to the affected lots and is issuing this recall out of an abundance of caution. The reliability of positive test results is not affected.
Detect is notifying all customers and distributors affected by the recall. Anyone in possession of any unused tests from the affected lots should dispose of the tests. The outer packaging is recyclable while all the test components can be discarded as regular trash. Detect Hubs are not affected by the recall and do not need to be discarded.
Test users who attempt to use recalled tests will be notified in the Detect App™ that the test has been recalled and may not be used.
Detect, Inc. will issue a refund* for the affected tests (as verified by Detect) upon customers’ acknowledgement of receipt of the recall-related communication and confirmation that any affected tests in possession have been disposed of.
Company name: Detect, Inc.
Brand name: Detect
Product recalled: Over the counter Covid-19 Test
Reason of the recall: There is an increased chance that the tests from the lot numbers listed below may give false negative results
FDA Recall date: December 12, 2022
Source: www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/voluntary-recall-three-detect-covid-19-test-lots
There is an increased chance that the tests from the lot numbers listed below may give false negative results. Detect has conducted a thorough investigation to identify this issue and has made the decision to conduct a voluntary recall for these lots. The reliability of positive test results is not affected.
Below is a list of the affected lots. The lot number can be found on the side of each test box along with the Use By date.
Lot Number: HB264, Use By Date: 1/1/2023, Number of Tests Shipped: 7,382
Lot Number: HY263, Use By Date: 1/1/2023, Number of Tests Shipped: 1,800
Lot Number: HY264, Use By Date: 1/1/2023, Number of Tests Shipped: 1,920
There is an increased chance that the tests from the lot numbers listed below may give false negative results. Detect has conducted a thorough investigation to identify this issue and has made the decision to conduct a voluntary recall for these lots. To date, Detect has not received any reports of false negative results related to the affected lots and is issuing this recall out of an abundance of caution. The reliability of positive test results is not affected.
Detect is notifying all customers and distributors affected by the recall. Anyone in possession of any unused tests from the affected lots should dispose of the tests. The outer packaging is recyclable while all the test components can be discarded as regular trash. Detect Hubs are not affected by the recall and do not need to be discarded.
Test users who attempt to use recalled tests will be notified in the Detect App™ that the test has been recalled and may not be used.
Detect, Inc. will issue a refund* for the affected tests (as verified by Detect) upon customers’ acknowledgement of receipt of the recall-related communication and confirmation that any affected tests in possession have been disposed of.
Company name: Detect, Inc.
Brand name: Detect
Product recalled: Over the counter Covid-19 Test
Reason of the recall: There is an increased chance that the tests from the lot numbers listed below may give false negative results
FDA Recall date: December 12, 2022
Source: www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/voluntary-recall-three-detect-covid-19-test-lots
305
a package that was not deliverd and they say it was, Rancho Jurupa Place, Pomona, CA, USA
2 months ago •reported by user-wxtwd114
i didnot receive my package through a lot of emails with euphoria-serenade they claim it was.they claim it was at the post office and sent me a label that is not a legit label per usps. this label has your address as sender usps does not have this item in there system
1.1K
QVC marketplace scam, Pomona, CA, USA
6 months ago •reported by user-xcmn8717
Ordered 4 chairs and didn’t receive. Two months later I contacted them and they said it was delivered. Time and date they said it was delivered I was home and Ring didn’t capture anything.
Customer service offered 50% back. I refused. Next day the offered 60%. Again …
Customer service offered 50% back. I refused. Next day the offered 60%. Again …
I refused. Then they offered 75% back.
Again I refused and said if I didn’t get full credit or the chairs I was calling my credit card company. Then they said they’ll credit full amount but it will take 2 weeks. They now had my money almost 3 months. I called credit card and disputed the charges said I never received it.
Do not fall for this scam!
Again I refused and said if I didn’t get full credit or the chairs I was calling my credit card company. Then they said they’ll credit full amount but it will take 2 weeks. They now had my money almost 3 months. I called credit card and disputed the charges said I never received it.
Do not fall for this scam!
702
Fraud, East Phillips Boulevard, Pomona, CA, USA
7 months ago •reported by user-cwwz7268
I did not order anything from this organization. I looked up the address and it is a now defunct landscaping company. The item I received was three small bottles of snail cream. The name on the return address is Paulette Douglas. I do not see on any
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my credit cards or bank account that anything was charged to me.
702
Unordered Package, 1313 East Phillips Boulevard, Pomona, CA 91766, USA
7 months ago •reported by user-yjqm6166
I received a ring in red box I did not order.THere is no receipt .
703
Ring I did not order, 1313 Phillips Boulevard, Pomona, CA 91766, USA
7 months ago •reported by user-dgbzw845
I received a GRA Moissanite ring that I did not order. It came from the same person that everyone else is getting one from. This is a different CA address though. Paulette Douglas, 1313 E Phillips Dr., Pomona, CA 91766
Im in Hope, Michigan, USA
Im in Hope, Michigan, USA
703
anonymous33258
I just got the same exact thing. Today. 8/22/23 Same name and address. I'm in MN.
- 7 months ago
- Reply
P
user-pcqqd856
received the same thing 8/17/23 and didn't order this...live in Greenville, SC. Been waiting for a bunch of items purchased through bed/bath and beyond out of business...thru a subsite, turns out it's coming from china, and my delivery info said the 45 items I ordered delivered and not 1 was a ring. scam...
- 7 months ago
- Reply
anonymous34145
I’m thinking that’s what has happened to me also. Ordered BBB and got a ring.
- 7 months ago
- Reply
anonymous34259
We also ordered through a BBB close out site and we received a ring today.
- 7 months ago
- Reply
anonymous34363
I too received a ring yesterday, and a cable cord today! No more discount ordering on the internet!
- 7 months ago
- Reply
anonymous34364
I placed an order what I thought was through Judy Blue and I received this same ring no clothing from 21460 YellowBrick Rd Walnut CA 91789
- 7 months ago
- Reply
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user-bxqjv545
I got the same ring but from a different address: 44211 Yucca Ave, Lancaster, CA, USA Yoshi Deals. I didn't order this.
- 2 weeks ago
- Reply
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3 days ago •reported by user-jbndt873
I ordered a plasma lighter that cost a lot of money, and also prepaid five dollars for the warranty for the plasma lighter I was supposed to get. Instead, I got a simple, butane torch lighter.
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Unordered delivery, 2800 North Franklin Road, Indianapolis, IN 46219, USA
2 weeks ago •reported by user-gwxgr728
I received a small package in the mail from them today. I didn't order it. I don't really even know what it is. It appears to be some kind of necklace that I would never wear much less order. Apparently, this was what I got instead of
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a Air Bed Self-Inflating Queen Size Air Mattress with Bilt-in Frame, pump and wheeled Case. Tracking number on the package matched the one attached to that item.
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Didn't get what I paid for, Princeton, IL, USA
3 weeks ago •reported by user-vjcyr133
I was supposed to receive a pallet of goods and I got 1 pair of wireless earbuds
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Honeywell Non-Sterile Eyewash Cartridge - recalled due to Non-compliance, USA
1 week ago •source www.fda.gov
Recall notice
Honeywell Safety Products USA, Inc. is voluntarily recalling Fendall 2000 Non-Sterile Eyewash Cartridge for the Fendall 2000 Eyewash Station. This recall is being conducted at the industrial consumer level. Honeywell’s supplier of the Fendall 2000 Non-Sterile Eyewash Cartridge has been found to be non-compliant with current good
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manufacturing practice (cGMP) requirements. To date, Honeywell Safety Products USA, Inc. has not received any reports of adverse events related to this recall.
The Fendall 2000 Non-Sterile Eyewash Cartridge is used for flushing or irrigating the eye to reduce chances of severe injury caused by acid, alkali, or particulate contamination. Product is contained in a 25-liter Ethylene-vinyl acetate (EVA) bag that is designed for use with the Fendall 2000 Eyewash Station. Only the Fendall 2000 refill cartridges are subject to this review, no other eyewash products. The saline eyewash solution contains purified water, benzalkonium chloride, edetate disodium, sodium chloride, sodium phosphate diabasic, and sodium phosphate monobasic. It is not marketed as sterile.
- Fendall 2000 Non-Sterile Eyewash Cartridge. Manufacturer’s Product Number/ Catalog Number: 32-002050-0000. Manufacturing Dates: 11-Oct- 2021 through 21-Jun-2023. Expiration Date: 11-Oct-2023 through 21-Jun-2025. Region: USA. Quantity: 6,954.
- Fendall 2000 Non-Sterile Eyewash Cartridge. Manufacturer’s Product Number/ Catalog Number: 32-002050-0000. Manufacturing Dates: 11-Oct- 2021 through 21-Jun-2023. Expiration Date: 11-Oct-2023 through 21-Jun-2025. Canada. Quantity: 3,651
Honeywell Safety Products USA, Inc. is notifying its distributors and customers by email, telephone or certified mail and is requesting anyone with product in its inventory to destroy or dispose of all units subject to the recall. Customers / distributors / retailers that have Fendall 2000 Non-Sterile Eyewash Cartridges should stop selling, shipping, and using the product immediately and destroy or dispose of it. Customers with questions regarding this recall can contact Honeywell Safety Products USA, Inc. by telephone.
Risk Statement: Use of or exposure to the eyewash without seeking medical attention afterwards could result in a range of ocular infections such bacterial keratitis or endophthalmitis. Immunocompromised individuals, those sustaining ocular injuries that damage the corneal epithelium, and those sustaining penetrating ocular injuries are at higher risk of potential infection.
Company name: Honeywell Safety Products USA
Brand name: Fendall 2000
Product recalled: Non-Sterile Eyewash Cartridge
Reason of the recall: Non-compliance with current good manufacturing practice (cGMP) requirements.
FDA Recall date: April 05, 2024
Source: www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/honeywell-safety-products-usa-inc-issues-voluntary-worldwide-recall-honeywell-fendall-2000-non
The Fendall 2000 Non-Sterile Eyewash Cartridge is used for flushing or irrigating the eye to reduce chances of severe injury caused by acid, alkali, or particulate contamination. Product is contained in a 25-liter Ethylene-vinyl acetate (EVA) bag that is designed for use with the Fendall 2000 Eyewash Station. Only the Fendall 2000 refill cartridges are subject to this review, no other eyewash products. The saline eyewash solution contains purified water, benzalkonium chloride, edetate disodium, sodium chloride, sodium phosphate diabasic, and sodium phosphate monobasic. It is not marketed as sterile.
- Fendall 2000 Non-Sterile Eyewash Cartridge. Manufacturer’s Product Number/ Catalog Number: 32-002050-0000. Manufacturing Dates: 11-Oct- 2021 through 21-Jun-2023. Expiration Date: 11-Oct-2023 through 21-Jun-2025. Region: USA. Quantity: 6,954.
- Fendall 2000 Non-Sterile Eyewash Cartridge. Manufacturer’s Product Number/ Catalog Number: 32-002050-0000. Manufacturing Dates: 11-Oct- 2021 through 21-Jun-2023. Expiration Date: 11-Oct-2023 through 21-Jun-2025. Canada. Quantity: 3,651
Honeywell Safety Products USA, Inc. is notifying its distributors and customers by email, telephone or certified mail and is requesting anyone with product in its inventory to destroy or dispose of all units subject to the recall. Customers / distributors / retailers that have Fendall 2000 Non-Sterile Eyewash Cartridges should stop selling, shipping, and using the product immediately and destroy or dispose of it. Customers with questions regarding this recall can contact Honeywell Safety Products USA, Inc. by telephone.
Risk Statement: Use of or exposure to the eyewash without seeking medical attention afterwards could result in a range of ocular infections such bacterial keratitis or endophthalmitis. Immunocompromised individuals, those sustaining ocular injuries that damage the corneal epithelium, and those sustaining penetrating ocular injuries are at higher risk of potential infection.
Company name: Honeywell Safety Products USA
Brand name: Fendall 2000
Product recalled: Non-Sterile Eyewash Cartridge
Reason of the recall: Non-compliance with current good manufacturing practice (cGMP) requirements.
FDA Recall date: April 05, 2024
Source: www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/honeywell-safety-products-usa-inc-issues-voluntary-worldwide-recall-honeywell-fendall-2000-non
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Unordered Package, Hamilton Township, NJ, USA
4 days ago •reported by user-zcwn4673
I received this cleaning stuff in the mail that I didn't order
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ACQRA ALLINREADINSS SCAM, London, UK
3 weeks ago •reported by user-qtmgq271
I’m ordering an electric scooter on 26/12/2023 and till today 20/03/2024 I don’t receive nothing. I’m already paying for it £45.55.
My order nr. 202312264734****.
I’ll appreciate very much if you can help with that.
Many thanks !
My order nr. 202312264734****.
I’ll appreciate very much if you can help with that.
Many thanks !
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Online Scam, NJ, USA
1 week ago •reported by user-vqqn8125
I ordered a device for unlimited Internet and received a adapter of some some sort. It was from Heathers MOTTY 2207 Summit Ave. Union City NJ 07087. I ordered internet device to receive unlimited Internet. They sent an adapter.
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Shipment, 192-01 Northern Blvd, Flushing, NY, USA
1 week ago •reported by user-jckz3224
I received keto gummies that I did not order.
Please cancel all shipments immediately.
Please cancel all shipments immediately.
Earrings, 125 Jackson Ave, Edison, NJ 08837, USA
1 week ago •reported by user-gwwbn779
I received a US Postal Service ground advantage package containing small red gem earrings. I did not order these earrings. Return address is Emily Hunt, 125 Jackson Ave., Edison, NJ.
Z
user-zfyxb379
I received almost the same earrings with a green stone. Same return address. I did not order these.
- 1 week ago
- Reply
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