Boil Water Advisory Lifted, Commerce Charter Township, MI, USA

2 years ago

Boil Water Advisory Lifted, Commerce Charter Township, MI, USA

Commerce Charter Township, Michigan, United States

Homeowners in Novi, Walled Lake, Commerce Township, and Farmington Hills have been advised that they no longer are advised to boil their water after the massive water main break at 14 Mile and Drake on Sunday.

Source: www.fox2detroit.com/news/novi-lifts-boil-water-advisory-after-water-main-break
Source publication date: 2021 11 03

#boilwateradvisorylifted #commercechartertownship #michigan #us

Related Reports

A
The Kansas Department of Health and Environment (KDHE) has rescinded a boil water advisory for the City of Kensington public water supply system located in Smith County. The advisory was issued because of a line break resulting in a loss of pressure in the system.

Source: hayspost.com/posts/8fbc6104-34cb-441f-b230-dcd3f2cfc977See More

Published: 2024-04-13
See Less

#boilwateradvisorylifted #kensington #kansas #us

A
A Boil water order has been lifted in Taylorville after water main repairs were made. The affected areas include 200 - 400 blocks of Pawnee Street, 200 - 600 Blocks of Wyandotte Street, 300 - 400 E Franklin Street, and 300 - 400 E Adams Street.

Source: … See More See Less

#boilwateradvisorylifted #pawneestreet #taylorville #illinois #us

A
Water in the city of Amsterdam is once again safe to drink. A boil water advisory had been in place since a water main break on Monday 8th. The advisory stayed through Wednesday morning, while testing was done.

Source: wnyt.com/capital-region-news/boil-water-advisory-lifted-in-amsterdam/
Published: 2024-04-10 See Less

#boilwateradvisorylifted #amsterdam #newyork #us

A
Thousands of households in Southeast Michigan are currently experiencing power outages due to severe storms that hit the area on Thursday. The outages are expected to continue until Friday morning. Utility companies have deployed their Storm Response Teams to restore power as quickly and safely as possible. … See More
It is important for residents to exercise caution during this time and stay at least 25 feet away from any downed power lines, as they are live and potentially dangerous. According to the latest updates from the utility company’s outage center, over 40,500 DTE Energy customers are currently without power as of 4:20 p.m.

Outage link: outage.dteenergy.com/map
Source: www.energyportal.eu/news/tracking-thousands-of-dte-energy-power-outages-in-metro-detroit/71655/
Published: 2023-07-20
See Less

#poweroutage #dteenergy #commercechartertownship #michigan #us

A
More than 20,000 are without power after winds as high as 50 mph blew through portions of Michigan. A large DTE outage between Clinton Township and Sterling Heights left over 2,500 customers without power. Two more outages affecting 1,500 to 2,500 people each were in North Brand … See More
Township and Hamtramck. Medium-sized outages affecting between 500 and 1,500 DTE customers hit Center Line, Detroit, Commerce and Goodland Township.

Outage link: outage.dteenergy.com/map
Source: www.detroitnews.com/story/news/local/michigan/2022/12/15/wind-advisory-issued-for-parts-of-michigan/69729975007/
Published: 2022-12-15
See Less

#poweroutage #dteenergy #commercechartertownship #michigan #us #ham #chi-chis

Recent Interesting Reports

T

An package from Heather s Motty, Union City, NJ, USA

3 weeks ago •reported by user-tjkd2133

I received a package from Heather s Motty Union City NJ today I have no idea what it is & no memory of ordering anything from them.

#unorderedpackage #delivery #unioncity #newjersey #us

D

user-dqfx6869

I ordered and received a product but when plugged into HDMI nothing happened, I would like to get my
Money back

C

user-cvgc6761

Got the same thing ,you plug it into HDMI?

In direct response to the Nurse Assist, LLC voluntary product recall initiated on November 6, 2023, for saline and sterile water medical products, Medline Industries, LP initiated a nationwide recall on November 15, 2023, for its Medline and Centurion branded convenience kits containing Nurse Assist 0.9% Sodium … See More
Chloride Irrigation USP and Sterile Water for Irrigation USP. The Nurse Assist recall was issued due to the potential for a lack of sterility, which could result in non-sterile products. Medline Industries, LP has received one adverse event associated with product manufactured by Nurse Assist.

Water-based medical products that are non-sterile and potentially contaminated could cause serious or life-threatening infections, including bloodstream, urinary tract, open wound/soft tissue, and respiratory infections. Patients who are elderly, critically ill, have weak immune systems (including newborn infants, pregnant women, and cancer patients), or have chronic diseases are particularly at risk of infection. However, other patients could also develop infections after exposure to contaminated water-based medical products.

The recall affects Medline and Centurion convenience kits that may be used at home by patients, caregivers, and home health providers, as well as convenience kits that may be used in medical settings for surgery or other medical procedures. Recalled kits include, but are not limited to, wound care kits, tracheostomy kits and catheter kits. A detailed list of recalled Medline and Centurion convenience kits, as well as an example of product labeling, can be found in the link below.

Consumers who have recalled product should stop using the product and contact Medline immediately.

Medline Industries, LP notified its direct distributors and consumers of the Nurse Assist recall by First Class Mail and email on 11/16/23, upon receipt of initial recall notification from Nurse Assist. Customers who received the recalled product were given instructions to quarantine all affected products immediately and provide Medline with a response regarding the affected quantity on hand. Upon confirmation of the affected quantity, Medline provided customers with over-labels to place on the affected inventory, with instructions for staff to remove the affected component before using the kit. The recall notification also instructed distributors and those who resold or transferred affected product to another company or individuals to notify their customers of this recall notification.

In case you experience 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. If symptoms persist, seek medical care.

Company name: Medline Industries, LP
Brand name: Medline and Centurion
Product recalled: Convenience kits
Reason of the recall: The potential for a lack of sterility
FDA Recall date: April 08, 2024

Source: www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/medline-industries-lp-issues-nationwide-recall-convenience-kits-containing-nurse-assist-09-sodium
See Less

#medicaldevices #recall #us

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 … See More
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
See Less

#recall #drugs #us

Create a Report

Please provide report title
Please provide location
Please provide details

Get alerts and updates for your case!

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

Skip this step

Add photos or video

We recommend photos and videos to help explain your report

Add Photo/Video
Skip this step

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

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.

Report by

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
Last 30 days