Adventist Health,1000 4th St, Tillamook, OR 97141
Latest report:
14 employees tested positive for Covid-19
2 years ago
14 employees tested positive for Covid-19 at Adventist Health in Tillamook County. Investigation Start Date: 9/2/2021, with the most recent onset of: 9/22/2021 New Cases of: 14
Source: www.oregon.gov
Source: www.oregon.gov
15
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Covid cases in my area are high, Rolla, MO, USA
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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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user-tnvv1773
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
…
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,
…
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
I recieved a package that I did not order., Tillamook, OR, USA
9 months ago •reported by user-prgn4337
I dont even know what these 3 items are. Some sort of buckle is my guess.
15
After the water samples tested negative and were verified by county environmental health the boil notice is lifted effective 2:41pm June 13th.
Source: www.tillamookcountypioneer.net/fairview-water-district-boil-notice-is-no-longer-in-effect-6-13-2023/
Published: 2023-06-13
Source: www.tillamookcountypioneer.net/fairview-water-district-boil-notice-is-no-longer-in-effect-6-13-2023/
Published: 2023-06-13
15
On Wednesday, March 15, 2023, at approximately 2:30 p.m. a 3rd party directional boring contractor drilled into a 12” ductile iron water main located at the intersection of 11th Street and Pacific Avenue. This resulted in a massive water leak that caused localized flooding and the closure
…
of 11th Street from Pacific Avenue to Laurel Avenue. Accordingly, the City worked with the State Health Authority and County Health Department to issue a boil water notice to the affected customers in that area.
Source: www.tillamookcountypioneer.net/city-of-tillamook-continued-emergency-road-closure-at-11th-boil-water-order-for-area/
Published: 2023-03-17
Source: www.tillamookcountypioneer.net/city-of-tillamook-continued-emergency-road-closure-at-11th-boil-water-order-for-area/
Published: 2023-03-17
15
43 employees tested positive for Covid-19 at Tillamook County Creamery Association in Tillamook County. Investigation Start Date: 13/12/2021, with the most recent onset of: 17/02/2022 New Cases of: 43
Source: www.oregon.gov
Source: www.oregon.gov
15
7 employees tested positive for Covid-19 at Tillamook County Creamery Association in Tillamook County. Investigation Start Date: 13-12-2021, with the most recent onset of: 21-01-2022 New Cases of: 7
Source: www.oregon.gov
Source: www.oregon.gov
15
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Unordered Product, Tampa, FL 33675, USA
4 weeks ago •reported by user-wmrjn444
I received 1 bottle containing 1oz of powder (did not open bottle)with a ship date of 3/5 and 1 bottle shipped 3/11 that I did not order. Called phone number 800-609-4174. Female answered phone but said she only speaks Spanish and she hung up. Immediately called back.
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She answered and I gave her my name & address and again she hung up. Immediately placed call #3 and inquired if anyone at her site spoke English ' again she hung up. I made one more call and left my phone number ' again another hang up. In process of reviewing all credit card charges. Tampa, FL, USA
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I received a product called Verti that I did not order and now sent another one, Tampa, Florida, USA
4 weeks ago •reported by user-wcdv4959
It came from Fulfilment Cemter
I got this package 2 weeks ago and another today I can't track where it came from
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522
Tejocote Dietary Supplements - recalled because it contains toxic yellow oleander, USA
5 days ago •source www.fda.gov
Recall notice
Global Mix, Inc. of New York, is recalling tejocote products to include the following brands: Eva Nutrition, Science of Alpha, Niwali, NWL Nutra. The recalled products are labeled as tejocote root but are toxic yellow oleander. The recalled products were distributed in the following states: AL, AK,
…
CA, CO, CT, DE, FL, GA, HI, ID, IL, IA, IN, KS, KY, LA, MD, MA, MI, MN, MS, MO, MT, NE, NV, NM, NC, NY, NJ, ND, OH, OK, OR, PA, SC, TN, TX, UT, VA, WA, WV, WI, and WY through website. The recalled products were also sold via the below websites via courier direct delivery and mail order. Etsy, amazon, eva-nutrition, tejocotemexican, niwali, scienceofalpha. The recalling firm has not received any reported of illness.
Recalled Products include the following bearing below information. Product codes and expiration dates can be found on the bottom of the packaging.
Product Name: Eva Nutrition MexicanTejocote root, Serial No: 181121U, Mfg Date: 08/01/2023, Expiry Date: 06/2025
Product Name: Science of Alpha Mexican Tejocote root, Serial No: 181121U, Mfg Date: 08/01/2023, Expiry Date: 06/2025
Product Name: NWL Nutra Mexican Tejocote root, Serial No: 181121U, Mfg Date: 08/01/2023, Expiry Date: 06/2025
Product Name: Niwali Mexican Tejocote root, Serial No: 181121U, Mfg Date: 08/01/2023, Expiry Date: 06/2025
Per the safety alert update on 3/12/24, "The FDA continues to receive adverse event reports related to the products identified in this Safety Alert."
The recall was the result of a routine sampling program by the company which revealed that the finished products contained the yellow oleander. The company has ceased the production and distribution of the product as the company continues their investigation as to what caused the problem. Further the company is conducting comprehensive quality control and monitoring process.
Customers who have purchased these products should stop using them immediately and return them to the point of purchase for a full refund.
Ingestion of yellow oleander can cause neurologic, gastrointestinal, and cardiovascular adverse health effects that may be severe, or even fatal. Symptoms may include nausea, vomiting, dizziness, diarrhea, abdominal pain, cardiac changes, dysrhythmia, and more.
If you are experiencing symptoms after eating this product it is important to report it. It can help to detect & resolve outbreaks early and prevent others from being harmed, and it enables better surveillance. If symptoms persist seek medical attention.
Company name: Global Mix, Inc.
Brand name: Eva Nutrition, Science of Alpha, Niwali, NWL Nutra
Product recalled: Tejocote Dietary Supplements
Reason of the recall: Product contains toxic yellow oleander.
FDA Recall date: April 10, 2024
Source: www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/global-mix-inc-recalls-tejocote-products-because-possible-health-risk
Recalled Products include the following bearing below information. Product codes and expiration dates can be found on the bottom of the packaging.
Product Name: Eva Nutrition MexicanTejocote root, Serial No: 181121U, Mfg Date: 08/01/2023, Expiry Date: 06/2025
Product Name: Science of Alpha Mexican Tejocote root, Serial No: 181121U, Mfg Date: 08/01/2023, Expiry Date: 06/2025
Product Name: NWL Nutra Mexican Tejocote root, Serial No: 181121U, Mfg Date: 08/01/2023, Expiry Date: 06/2025
Product Name: Niwali Mexican Tejocote root, Serial No: 181121U, Mfg Date: 08/01/2023, Expiry Date: 06/2025
Per the safety alert update on 3/12/24, "The FDA continues to receive adverse event reports related to the products identified in this Safety Alert."
The recall was the result of a routine sampling program by the company which revealed that the finished products contained the yellow oleander. The company has ceased the production and distribution of the product as the company continues their investigation as to what caused the problem. Further the company is conducting comprehensive quality control and monitoring process.
Customers who have purchased these products should stop using them immediately and return them to the point of purchase for a full refund.
Ingestion of yellow oleander can cause neurologic, gastrointestinal, and cardiovascular adverse health effects that may be severe, or even fatal. Symptoms may include nausea, vomiting, dizziness, diarrhea, abdominal pain, cardiac changes, dysrhythmia, and more.
If you are experiencing symptoms after eating this product it is important to report it. It can help to detect & resolve outbreaks early and prevent others from being harmed, and it enables better surveillance. If symptoms persist seek medical attention.
Company name: Global Mix, Inc.
Brand name: Eva Nutrition, Science of Alpha, Niwali, NWL Nutra
Product recalled: Tejocote Dietary Supplements
Reason of the recall: Product contains toxic yellow oleander.
FDA Recall date: April 10, 2024
Source: www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/global-mix-inc-recalls-tejocote-products-because-possible-health-risk
303
Subgenix, Perkins Park Drive, Akron, OH, USA
2 weeks ago •reported by user-kcbc7682
I didn't order,came in a white bag.
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