Power Outage, Springvale, San Antonio, TX 78227, USA

1 year ago

Power Outage, Springvale, San Antonio, TX 78227, USA

San Antonio, 78227 Texas, United States

As a cold front moved in, San Antonio firefighters and CPS Energy crews responded to electrical fires and power outages across the city. As of 7:30 a.m., 89 power outages were affecting more than 5,700 customers, and 14 electrical fires were reported by SAFD.

Outage link: outagemap.cpsenergy.com/
Source: www.ksat.com/news/local/2022/10/17/electrical-fires-power-outages-pop-up-around-san-antonio-amid-light-rain/
Published: 2022-10-17

#poweroutage #sanantonio #texas #us

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Outage link: www.consumersenergy.com/outagemap
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Yeah I'm very disappointed y'all charged way too much money I go spend about 85 bucks come home after work to my family to find that u forgot 2 quesadilla beef fajita plates So if You're going to be charging a lot of money for y'all's f****** … See More
food then own up to it instead of not giving a s*** cuz it's really f****** annoying and I'm pissed cuz this doesn't happen once I go there a lot cuz your food is good but y'all f****** too many f****** times Why don't you give people raises and stop hiring f****** rookie ass little kids It's annoying Now I got to go back pick up two f****** plates Like if I want to go f****** do that I'm f****** tired I work all day so what the f*** this is b*******.....
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V

user-vbcjd822

I hate all Manna Margie's restaurants! Way too expensive and their food is horrible! I stopped buying good from there years ago and have never returned! That's my way of boycotting there establishment!

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Hours after 2,500 customers were without power Tuesday morning, March 26, another major outage has struck more than 1,500 CPS Energy customers on the Northeast Side of San Antonio, namely in the Medical Center around the intersection of Babcock Road and Huebner Road, are without power Tuesday … See More
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Outage link: outagemap.cpsenergy.com/
Source: www.lmtonline.com/news/local/article/power-outage-san-antonio-19369765.php
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CPS Energy was reporting a power outage on the city’s West Side that left more than 2,500 customers without power early Tuesday morning, Mar 26. According to the CPS Energy outage map, power was restored around 6 a.m.

Outage link: outagemap.cpsenergy.com/
Source: www.ksat.com/news/2024/03/26/power-outage-reported-citys-west-side-early-tuesday-morning/
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#poweroutage #sanantonio #texas #us

Recent Interesting Reports

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user-dqfx6869

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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
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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
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