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Power Outage, Portland, MI, USA

1 month ago

Portland, 48875 Michigan, United States

Planned 12 Hour City-Wide Power Outage set for October 15th

Source: theportlandbeacon.com
Source publication date: 2021 09 17

166


Related Reports

Power was restored for Duke Energy customers in the downtown Jeffersonville area after about a 45-minute outage Tuesday afternoon. About 4,000 Duke Energy customers in Jeffersonville lost their electricity about 3:30 p.m. Tuesday.

Source: newsandtribune.com
Source publication date: 2021 10 19 See Less


Dominion Energy’s outage map showed 6,237 outages at 2:30 p.m. An official with Dominion said all the power was restored in Norfolk before 3 p.m. The outage hit several neighborhoods, including parts of Lafayette-Winona, Lakewood, Fairmont Park, Ballentine Place and Coleman Place.

Outage link: outagemap.dominionenergy.com
Source: wavy.com ... See More Source publication date: 2021 10 19 See Less


A pair of power outages are once again impacting the Rough and Ready and Penn Valley areas Wednesday morning, according to PG&E’s online outage map.
Today, 2,109 PG&E customers were without power. Tuesday’s outages impacted the same number of customers in the same area, according to PG&E’s... See More map.
The outages were reported around 8 a.m.

Outage link: m.pge.com
Source: theunion.com
Source publication date: 2021 10 20
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Entergy announced a planned power outage for parts of Central City Wednesday. Areas around Martin Luther King Jr. Boulevard near the King Rampart Apartments will experience a power outage as workers upgrade circuits. The power outage is scheduled between 7 a.m. and 4 p.m.

Source: wdsu.com
Source... See More publication date: 2021 10 20 See Less


Colorado Springs Utilities worked to restore power to more than 1,300 residents who lost electricity Wednesday morning.
Neighborhoods between North Academy Boulevard, East Platte Avenue, Palmer Park Boulevard and North Circle Drive lost power shortly after 9:30 a.m. after a construction crew hit a power line in... See More the area.

Source: gazette.com
Source publication date: 2021 10 20
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A pair of power outages are once again impacting the Rough and Ready and Penn Valley areas Wednesday morning, according to PG&E’s online outage map.
Today, 2,109 PG&E customers were without power. Tuesday’s outages impacted the same number of customers in the same area, according to PG&E’s... See More map.
The outages were reported around 8 a.m.

Outage link: m.pge.com
Source: theunion.com
Source publication date: 2021 10 20
See Less


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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Central Maine Power is working to restore power in the Sebago area after a Maine Department of Transportation dump truck hit a CMP pole Wednesday morning on Peabody Pond Road.
As of 1:20 p.m., CMP reported about 90 customers still without power.

Source: newscentermaine.com
Source publication date:... See More 2021 10 20 See Less


A power outage affecting thousands of PG&E customers in Oakland on Wednesday was caused by rainy and windy weather in the area.
The outage was first reported at 10:49 a.m. and affected 3,935 customers at its peak.
The utility's outage map showed neighborhoods on both sides of... See More Broadway north of West MacArthur Boulevard affected by the outage.

Source: ktvu.com
Source publication date: 2021 10 20
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The power is out in several parts of Carmel, affecting a little over 2,000 people. PG&E said the power is going to be out until 5:30 p.m. today.

Outage link: m.pge.com
Source: kion546.com
Source publication date: 2021 10 20 See Less


Recent Interesting Reports

FROMM FAMILY FOODS is issuing a voluntary recall of approximately 5,500 cases of Fromm Shredded can Entrée dog food due to potentially elevated levels of Vitamin D.

Consumers should stop feeding the products listed below to their dogs. Potential adverse reactions could occur in all size dogs. ... See More No reports of illness or injury have been reported from consumers to date, however Fromm management has determined it is prudent to pull these four lots out of distribution.

Affected recalled products were distributed at neighborhood pet stores nationwide.

Products are packaged in 12 oz. cans with Best By Date 08/2024. A full list of affected products is:
- Four-Star SHREDDED BEEF IN GRAVY ENTRÉE food for dogs, 12 cans per case, 11877, 12 oz. per can, UPC: 7270511876, Best By Date 082024
- Four-Star SHREDDED CHICKEN IN GRAVY ENTRÉE food for dogs, 12 cans per case, 11881, 12 oz. per can, UPC: 7270511880, Best By Date 082024
- Four-Star SHREDDED CHICKEN IN GRAVY ENTRÉE food for dogs, 12 cans per case, 11879, 12 oz. per can, UPC: 7270511878, Best By Date 082024
-Four-Star SHREDDED TURKEY IN GRAVY ENTRÉE food for dogs, 12 cans per case, 11883, 12 oz. per can, UPC: 7270511882, Best By Date 082024

Dogs ingesting elevated levels of Vitamin D may exhibit symptoms such as vomiting, loss of appetite, increased thirst, increased urination, excessive drooling, and weight loss. Vitamin D when consumed at very high levels can lead to serious health issues in dogs including renal dysfunction. Consumers who have dogs that have consumed any of the affected products and are exhibiting these symptoms should contact their veterinarian.

Check the full recall details on fda.gov

Company name: Fromm Family Foods
Brand name: Fromm Four-Star Nutritionals
Product recalled: Shredded Entrée canned dog food
Reason of the recall: Elevated levels of Vitamin D
FDA Recall date: October 01, 2021

Source: FDA
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95


Shipment arrived at Teterboro Center on 10/14. No movement since. Teterboro Center is located about 5 minutes from my house. 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." See Less
5.1K


Minneapolis, Minnesota, IntegraDose Compounding Services is voluntarily recalling nine lots, listed in the table below, of cefazolin 2 gram in 20 mL syringe for injection and two lots of cefazolin 3 gram in 100 mL 0.9% sodium chloride bag for injection due to a lack of sterility... See More assurance resulting from compounding in a newly installed biologic safety cabinet without completing dynamic smoke study testing.

Intravenous administration of a non-sterile drug could result in serious infections ranging from fever, chills, and malaise, to severe adverse events such as septicemia, bacterial meningitides, and wound infection which may be life-threatening. The possibility of a breach in sterility assurance in distributed products, while not confirmed, cannot be eliminated. No batches of the product have been identified as containing microorganisms. To date, IntegraDose Compounding Services has not received reports of any adverse events associated with this issue for these lots.

- Cefazolin 2 gram in 20 mL syringe for injection. (See link below for a detailed list of Lots)
- Cefazolin 3 gram in 100 mL 0.9% sodium chloride bag for injection. (See link below for a detailed list of Lots)

Cefazolin is an antibiotic and the products are packaged in zip-locking bags containing ten units. The lots were distributed nationwide in the USA to hospitals from 8/12/21 to 9/15/21. IntegraDose Compounding Services has initiated an investigation to determine the root cause and corrective and preventative actions.

IntegraDose Compounding Services has notified its direct customers via a recall letter and is arranging for the impacted product to be returned. Anyone with an existing inventory of the recalled lots should stop use and distribution and quarantine immediately.

Consumers with questions regarding this recall can contact IntegraDose Compounding Services by phone at (612-672-5216) on Monday - Friday, 8:00 AM – 4:00 PM CDT.

Company name: IntegraDose Compounding Services, LLC
Brand name: IntegraDose Compounding Services, LLC
Product recalled: Cefazolin
Reason of the recall: Lack of sterility assurance.
FDA Recall date: September 21, 2021

Check the full recall details on fda.gov

Source: FDA
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95


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
5.1K


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
17


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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This is the 2nd package that just arrives at teterboro and just stops moving what’s the point of charging for next day air if you can’t get it done .. worse thing about this is that’s it’s anxiety medication i desperately need See Less
5.1K


HA
Hate USPS
I wonder if we could all group together and file a class action lawsuit. I saw another post here with two tracking #s stuck from October 1st and Sept 28th that haven’t moved yet.
Reply 5 days ago
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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