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The city of Ivey was under a boil advisory for the areas around Morningside Drive and South Lakeview Drive. The boil advisory is due to a valve installation, which caused the water to have to be turned off in those impacted areas.
February 28, 2021 12:00 PM
“A boil water advisory was issued for Fort Lauderdale’s Victoria Park neighborhood on Feb 27.
Source: wsvn.com ”
Recent Interesting Reports
February 15, 2021 1:00 AM
“I ordered 2 chainsaws from an ad on the internet which popped up while playing cards on my phone from a web company called Blackcass.com. I thought that I was ordering rechargable woodcutter/chainsaws, but received two chains instead. They would not refund my money or allow me to return and get a re... fund. They said that I had ordered the chains when I only see a big picture of a chainsaw. Their website is misleading to say the least. I would say I was scammed. They also scam people on their website with another chainsaw they are selling that has the well known brand name of Stihl on the saw. Then they send you an off brand saw made in China. Fraud indeed! ”
February 5, 2021 8:50 PM
“I received my first vaccine at Alamodome on January 20 and will get second vaccine February 10. The Alamodome was very organized and the people who worked there very professional. I had no reactions to first shot which was Pfizer ”
February 13, 2021 3:46 PM
“I bit and bought a $30 GT A26 saw and found out after I had ordered it, that it was only a chain. I contacted the company and said I wanted to upgrade to the $60 chainsaw that was on their website and they said no problem & I would get the whole thing. I just received it and it is a completely diff... erent chainsaw and now the saw is not on their website anymore. Wondering how I can get my money back. ”
February 12, 2021 3:09 PM
“Blackcass, 2020 Hot Selling-GTA 26 Battery-Powerd Wood Cutter is what I ordered- said it was a stihl model- including case- did not recieve that- have an off brand no case :(not stihl gta-26 model ”
February 11, 2021 6:25 PM
“I did very well with my first shot of Moderna. I had no reaction except a very sore arm at the injection sight. ”
February 11, 2021 5:22 PM
“Got my second Moderna Covid-19 vaccine shot, no side effects this time. A little tired and thirsty but so far so good. ”
February 6, 2021 5:43 PM
“I have read the other reports and totally agree this is a scam. I thought I purchased the Stihl battery cutter shown with a hand saw in the bubble. It said $29.99 so that's what I sent. The orange handled saw arrived but not the cutter. I emailed the company and they said that was what I bought. I h... ad to click the cutter box it showed $89.99. I really liked what was advertised so I paid it. (The hand saw definitely wasn't worth $29.99 and I thought it was a gift for getting the cutter) When the cutter arrived, it was a cheap black handsaw. Came in a cardboard box not a nice carrying case. It had a small slip on guard but not the guard and shield as advertised. There was no chain saw oil. They both had charger base and battery. I emailed them back saying this was fraud. Jennifer from the company emailed back and said she was sorry about my being disappointed. I was not to send the product back. I was to send a picture of what I got, tracking number and SKU from box. I took these pictures and sent a picture of what I was promised. There was no SKU # on box. She emailed me back and said I should not return it because it could get lost going to Hong Kong and without the product there would not be a refund. She said it probably wouldn't pass customs. I should give it as a gift and person will really like it! I wrote to the Better Business Bureau and hope to find out next step. Her comments make me fearful to return. ”
March 3, 2021 8:00 PM
“Company name: Ridley Block Operations
Brand name: Ridley Block Operations
Product recalled: CRYSTALYX Sheep-lyx
Reason of the recall: Elevated levels of copper
FDA Recall date: March 03, 2021
Recall details: Ridley Block Operations is voluntarily recalling three batches of CRYSTALYX Sheep-lyx.... The product batches have been found to have elevated levels of copper, which is out of specification. With prolonged consumption, the affected product could potentially have adverse health effects on sheep. This recall relates only to CRYSTALYX Sheep-lyx with the following batch/lot numbers printed on the package:
- CRYSTALYX® Sheep-lyx™. B01769272. Item No./Product No: 7248. Package Info: 125# Block
- CRYSTALYX® Sheep-lyx™. B01769338. Item No./Product No: 7248. Package Info: 125# Block
- CRYSTALYX® Sheep-lyx™. B01769344. Item No./Product No: 7248. Package Info: 60# Block
No other batch/lot numbers or other Ridley Block Operations products are involved in this voluntary recall. Only the specific batches and lot numbers of CRYSTALYX Sheep-lyx listed above are impacted. No injuries or illnesses have been reported.
Ridley Block Operations has notified its customers of this voluntary recall. Products matching these batch/lot numbers should be removed from distribution/inventory and discontinued from feeding. Customers are encouraged to call Ridley Block Operations customer service at 1-903-480-0021 (Monday – Friday, 8:00 a.m. - 4:00 p.m. CT) for instructions on what to do with affected product inventory.
Check the full recall details on fda.gov
Source: FDA ”
February 19, 2021 5:13 PM
“I choose not to get the injection because as a Big Pharma trained drug rep, realized Pfizer, Moderna, and AZ were only given Emergency’ FDA approval and skipped the animal trials. The jab offers NO immunity nor does it stop transmission; it is therefore NOT a vaccine. It is nothing more than Expe... rimental Biological Agent for a virus with a 99% survival rate (without any intervention. There are much saver therapeutics. He only benefit to the jab is a lessened symptom. The CDC updates the adverse events every Friday. As you can see from their last report, over 900 have already died and over 11,000 have sustained serious injuries.
The risk/return isn’t favorable. It takes about 7 yrs to develop a vaccine. This is way too soon. ”
February 3, 2021 1:00 PM
“Company name: Apotex Corp
Brand name: Apotex Corp.
Product recalled: Enoxaparin Sodium Injection, USP
Reason of the recall: Packaging error resulting in incorrect dosage listed
FDA Recall date: February 03, 2021
Recall details: Apotex Corp is voluntarily recalling two (2) batches of Enoxaparin... Sodium Injection, USP to consumer level due to a packaging error resulting in some syringes barrels containing 150 mg/mL markings (corresponding to 120 mg/0.8mL strength) instead of 100 mg/mL markings (corresponding to 100 mg/mL strength) on the syringe barrel and vice versa. The packaging error was discovered during a customer complaint investigation. To date, Apotex has not received any reports of adverse events related to use of these two batches. The affected product is manufactured by Gland Pharma Limited, Hyderabad, India.
Health Hazard Assessment: Incorrect syringe barrel marking could lead to miscalculation and inaccurate dose administration to patients. In one recalled batch (batch CS008, strength 100 mg/mL), if a consumer used a 150 mg/mL concentration packaged in a barrel corresponding to a l00 mg/mL concentration, patients could receive 3.75 mg of Enoxaparin, instead of 3 mg of Enoxaparin. In another recalled batch (batch CT003, strength 120 mg/0.8mL), if a consumer used a 100 mg/mL concentration packaged in a barrel corresponding to a 150 mg/mL concentration, patients would receive 2 mg of Enoxaparin rather than 2.5 mg of Enoxaparin. Accidental overdosage following administration of enoxaparin sodium injection may lead to bleeding complications. Alternative, if the dose administered is less than prescribed, the patient may be subject to developing some blood clotting conditions.
Enoxaparin Sodium injection is indicated for the prophylaxis of deep vein thrombosis (DVT), which may lead to pulmonary embolism (PE), Treatment of Acute Deep Vein Thrombosis, prophylaxis of ischemic complications of unstable angina and non-Q-wave myocardial infarction, when concurrently administered with aspirin and Treatment of Acute ST-Segment Elevation Myocardial Infarction.
The affected Enoxaparin Sodium Injection, USP can be identified by NDC numbers stated on carton and label of the product.
Product: Enoxaparin Sodium Injection, USP
Batch #: CS008
Strength: 100 mg/mL
Syringe Barrel Measurement Markings: 100 mg/mL
Pack Size: 10 x 1mL Single Dose Syringes
NDC NumberOn Carton: 60505-0795-4
NDC Number On label: 60505-0795-1
UPC Code on Carton: 360505079544
UPC Code on label: (01)10360505079510
Product: Enoxaparin Sodium Injection, USP
Batch # : CT003
Strength: 120 mg/0.8mL
Syringe Barrel Measurement Markings: 150 mg/ mL
Pack Size: 10 x 0.8 mL Single Dose Syringes
NDC NumberOn Carton: 60505-0796-4
NDC Number On label: 60505-0796-0
UPC Code on Carton: 360505079643
UPC Code on label: (01)10360505079602
The two (2) affected batches of Enoxaparin Sodium Injection, USP were distributed by Apotex nationwide in the USA to Wholesalers and Warehousing Chains. Apotex Corp. is currently notifying its affected direct account Wholesalers and Warehousing Chains, via mail (FedEx Standard Overnight) by mailing a recall notification letter and is arranging for return of all recalled product.
Check the full recall details on fda.gov
Source: FDA ”