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Boil Water Advisory, Woodward Ct, Lehigh Acres, FL 33936, USA
1 month ago
Woodward Court, Lehigh Acres, 33936 Florida, United States
The Florida Governmental Utility Authority (FGUA) issued a Precautionary Boil Water Notice Advisory for Lehigh Acres system customers Friday. A scheduled shutdown at 1297 Woodward Court required the shutdown area to expand due to a valve failure. According to FGUA, approximately 300 customers residing on Woodward Court from Beth Stacy to Westminster Street N., including Broad Street N., Vineyard Street, Westley Street, Westminster Street W., Broad Street W., and Sunshine Way may have experienced low pressure or no water.
Published: 2022 04 22
Sauquoit residents who live on Paris Hill Road from Oneida Street to the Paris Hill tank are under a boil water advisory until further notice.
A boil water notice has been issued for the city of Buffalo Gap. According to city officials, the notice is in effect for the old Aqua Source customers in the Buffalo Gap area until further notice.
The Slate Springs Water Association in Monroe County has issued a Boil Water Notice until further notice for all of its customers.
A boil water notice has been issued by the Arnold Line Water Association. The notice is expected to affect around 330 customers around the Shears Road Apartments, West Lane, North Lane and South Lane; Hillcrest Drive, including the Magnolia Apartments and Weathersby Road from Lowes to the... intersection of Shears Road and Hillcrest Drive.
11 hours ago
Residents in Ridgetop, Tennessee are urged to boil their water due to it potentially being contaminated with fecal coliform or E. coli.
A boil water order was put into effect at 10:30 a.m., Friday, May 27, for the Parthenon Water Association for its customers on Gum Springs Road, Smith Mountain Road, Lone Beech Road and Murray Road. The order is due to tank maintenance work.
Recent Interesting Reports
4 weeks ago
I ordered something from MI that went to the teterboro distribution center after passing through the metro NY center, which makes no sense since the final destination is in NY. It has been sitting there for 4 days with no movement. I’m getting really nervous about whether... my package will arrive. I need what’s in that box. No response to my inquiries thus far.
I order an Africa fabric from amazon. it was sent to the USPS Avenel NJ location via SF Express. my package was scanned in that facility at 9.05am on 4/11/2022 until now 4/29/2022 my package is seating in that facility. I have no information. Why is my package not being delivered?
1 week ago
I have had two packages that have 'gone missing' with USPS and have now had to refund customers. The packages never seem to leave NJ and both contained the same single items (a CD). The first small media mail package was sent on March 15th, 2022 -->... Departed post office in Pitman, NJ on Mar 15 --> arrived at South Jersey NJ Distribution Center March 15 @ 3:54pm --> March 19th - In transit to next facility and no updates after that. During April: spent a few calls completing the 'missing mail' forms both electronically and speaking to 'investigators' who promise to call back. When I receive call-backs it's to say that my missing mail electronic form 'wasn't fully filled out' or that 'the missing report action has not been updated' or that they are 'now pushing it forward.' No notifications from the USPS since then. My second package that I am going to have to refund the customer for was another small media mail package with CD sent April 25th 2022 --> USPS in possession from Sewell NJ --> April 25 2022 Departed Post Office Sewell NJ --> April 29 2022 "In transit, arriving late". It is now May 17th and still no package to the customer.
2 weeks ago
I just opened My package and the sunglasses are in many pieces broken and I wanted to wear them next week on My trip to Annapolis to see My Granddaughter Graduate the Naval Academy
Heartland farms about dog food I purchased. I bought the big bag of heartland farms dog food yesterday and tonight my dogs got sick and got diarrhea | Symptoms: Diarrhea
Driver completely destroyed my yard as well as my cement planter that is my property marker. They decided to use my yard as a short cut through to the main road. They took out my cement planter in the process. It had a flagged reflector so there... was absolutely no reason they could of not seen it there. When approaching the van, they decided to hop back into the van and sped off while destroying my yard in the process. They endangered my mothers safety when she went to approach the situation. Their reckless driving is a safety concern and could of caused my mother bodily harm
Teva Pharmaceuticals USA has initiated a voluntary nationwide recall of a single lot of Anagrelide Capsules, USP 0.5 mg (Lot number GD01090), to the consumer level in the United States. This voluntary recall was initiated due to dissolution test failure detected during routine stability testing. No other... lots are impacted.
The recalled product is:
Anagrelide Capsules, USP 0.5 mg
Lot # GD01090
Exp. Date 05/2022
Administration of this product with lower dissolution – taking longer to dissolve once ingested -- may result in decreased effectiveness or ineffectiveness of the drug to exert its platelet-reducing effect. Failed dissolution can result in a slower rate and extent of drug release leading to less anagrelide available in the body. For seriously ill patients with elevated platelet counts, less available anagrelide in the body could increase the risk of clotting (blood coagulation), and clotting or bleeding events such as a heart attack or stroke, which could be life-threatening. To date, Teva has not received any product quality complaints or adverse event reports, of this nature, for the recalled lot.
Anagrelide capsules are indicated for the treatment of patients with thrombocythemia, secondary to myeloproliferative neoplasms, to reduce the elevated platelet count and the risk of thrombosis and to ameliorate associated symptoms including thrombo-hemorrhagic events. Information about the affected lot is listed in the table below. It is packed in bottles with 100 Capsules. Teva distributed 4224 bottles nationwide from 07-30-2020 through 09-02-2020 to its wholesale, distributor and retail customers under the label for Teva Pharmaceuticals USA, Inc.
Company name: Teva Pharmaceuticals USA
Brand name: Teva
Product recalled: Anagrelide Capsules
Reason of the recall: Dissolution Test Failure
FDA Recall date: May 23, 2022
Last thing eaten was a sandwich at a Law Enforcement Appreciation meeting. 5/19/2022 in Englewood Fl. Next day feeling very sick, felt cold but no fever., then vomitting, heavy trembling, somewhat incoherent. | Symptoms: Vomiting, Shaking
St. Paul, Minnesota, Fagron Inc. (“Fagron”) is voluntarily recalling two lots of SyrSpend SF Cherry to the hospital, pharmacy, and distributor level out of an abundance of caution. The affected lots are potentially contaminated with Burkholderia gladioli.
Burkholderia gladioli is an opportunistic pathogen most commonly affecting patients... with respiratory disease. Patients with compromised immune systems such as those with Cystic Fibrosis are at higher risk. Burkholderia gladioli also can cause complications after transplants. Exposure to contaminated product could lead to adverse events, which could be severe for at-risk individuals.
Fagron has received three complaints regarding an undesirable smell associated with the product. To date, Fagron has not received any reports of adverse events related to the product being recalled. Fagron sells this product for the extemporaneous compounding of prescriptions for oral dosing. The affected lots with expiration dates are listed below.
Item number: 805359
Size: 500 mL
NDC number: 51552-1123-5
Expiration date: 08/31/2024
Item number: 802496
Size: 4 L
Expiration date: 08/31/2024
Fagron has already notified its distributors and customers by phone, e-mail, and/or letter and is arranging for return of all recalled products. Hospitals, pharmacies, and distributors that possess affected product should quarantine this material and await further instructions from Fagron or Fagron’s recall coordinator. Please immediately discontinue use or distribution of the recalled product. Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to taking or using this product.
This recall is being conducted with the knowledge of the U.S. Food and Drug Administration.
Company name: Fagron Inc.
Brand name: Fagron
Product recalled: SyrSpend SF 500mL and 4L
Reason of the recall: Potential contamination with Burkholderia gladioli
FDA Recall date: May 02, 2022