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825 West Roybal Drive, Las Vegas, New Mexico, United States
Updated: January 25, 2022 12:00 PM
3 months ago
Multiple employees(4) at YOLANDA VALDEZ in LAS VEGAS, NM tested positive for Covid-19 and the company is on the Rapid Response COVID-19 Watchlist Event Date: 01/26/2022,
Recent Interesting Reports
Something is very wrong with the billing periods as well as the billing, my bill are always through the roof & when I’m paid up they’re always sending outstanding bills & when I call they always claim I’m behind & that isn’t true every month my bill... is over three hundred but my monthly usage is only one hundred so how is this even possible, I need some help here please investigate fairly & truthfully someone, I and the others who are like me thank you so much, no one is above the law & no one should be taken advantage of.
I purchased 2 battery powered chainsaws on June 29, 2021. (The receipt is attached) What I received 6 to 8 weeks later was not what I have ordered. Both my receipts shows item description and booths says battery powered chainsaws ×2. Wheni have contacted the store they... kept telling me it was shipped and showed to be delivered. Picture of what I received is attached. Would you kindly explain to me if what I received is a battery powered chainsaw please let me know how to use it becaus I clearly cannot see battery or chain on it. Was all the pieces sent for it. Honestly it does not look anythin like chainsaw to me. But i do wear eyeglasses and have a disability. But still I kow what chainsaw looks like. Product from China - Hahdiy.
1 week 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
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.
Foldable Car Door Step Stand Pedal - Access to Vehicle's Top Roof Both Feet Stand Pedal Ladder for Most SUV Truck Jeep Black (Fit F150), United States
4 weeks ago
A product being advertised on Amazon and across social media, a detachable step plate that attaches to the latching mechanism of a vehicle and rests in the door jamb, has the potential to cause severe injury or death, damage to vehicles, and potential harm to bystanders. It... poses a major fall risk, braces against a part of the vehicle that can be damaged easily, can cause broken bones and the chance of slamming the head against the vehicle and ground causing severe injury, laceration, impaction, and death from the fall. It is a direct threat to the elderly, children, and the average targeted consumer. Under no circumstances is this product ok to be selling at all. That spot of your car is not mean to hold that much weight under those circumstances. Repeated stress on that weakens it. It also pulls it out of alignment in small increments causing progressive worsening of stressors on the door hinges, the weather stripping and seals on the door from extra pressure along the bottom, and potential problems with the locking mechanism so that one day when you think it's locked it won't be. Or the latch decided to not properly catch and opens while driving. Not to mention the lack of propper safety measures for yourself in this instance alone. The step plate can easily rotate under the foot and become dislodged due to stress on the locking mechanism and pressure on the door jamb where it's not intended to be placed. Not all vehicles have the same door jamb construction either making this even more of a risk that it doesn't rest in the same way on all vehicle models posing even more threat to the user and the property around them plus the vehicle.
Perhaps even more concerning is at least one model mentions that "The wide platform of the pedal offers plenty of stability, enough room for nearly both feet, and can safely hold up to 400lbs." NEARLY both feet. This is even more concerning as it tells the consumer that you can't fully rest your entire self safely on the product as they intend you to. You can't prevent a fall if you can't even fully stand on the step. It also fails to address what size foot it is referring to in the first place. Foot sizes vary greatly. This product and all others like it being sold are extremely dangerous and are putting lives at risk and utilizing a part of a vehicle in a way strictly forbidden by vehicle manufacturers for the safety of the consumer. This may even void the warranty of the vehicle in some cases of damage.
For an example of one of the offending products you can see the following listing on Amazon.com
Also note in this particular version that it states it sits even higher than others like it increasing the chance and risk involved as well. The trend of these devices on social media is alarming. And the threat is great.
See the following for an example on social media: facebook.com
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
It's a sexual supplement, called Captain Boss Bully Ruby 10000. My wife and I both took one each. We both started shaking horribly uncontrollably, our heads started throbbing, and we started sweating profusely. I started throwing up she didn't. Both of us had problems with our eyes.... Eyes were bloodshot red and super glassy. Don't know what's in those but it's nothing like the pink pussycat pill or the Rhino pills. | Symptoms: Nausea, Vomiting, Sweating, Shaking
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
Natural Organics, Inc., is voluntarily recalling four lots of NaturesPlus Keto Living Sugar Control Capsules 90 count, because it was found to contain gluten. People who have allergies to wheat or gluten run the risk of serious or life-threatening allergic reactions if they consume these products. There... have been no reported incidents of illness or adverse reactions in connection with these products to date.
Individuals with Gluten intolerance may experience minor to severe reactions after consuming this product. This could include upset stomach, diarrhea, fatigue, skin reactions and more. It was discovered during routine testing that the product contains gluten. It was subsequently discovered that a raw material that is normally gluten free tested positive for gluten.
Gluten is a general name for the proteins found in wheat (wheatberries, durum, emmer, semolina, spelt, farina, farro, graham, KAMUT® khorasan wheat and einkorn), rye, barley, and triticale – a cross between wheat and rye.
The listed products were distributed nationwide to consumers, retail stores and to the following foreign countries: Kenya, Spain, Trinidad, United Arab Emirates, and the United Kingdom. The capsules are packaged in white jars and black caps; with labels having orange, white and black print bearing the product codes, lot numbers and “Best By” or “BBE” (Best Before End) dates are printed on the bottom of the bottle.
The lots affected are:
- NATURES PLUS KETO LIVING SUGAR CONTROL CAPSULES, 90 CAPSULES, Product No. 82004, UPC Code 097467820043, Lots 1362073, Best By 10/2025 and 1365200, Best By 10/2025
- NATURES PLUS KETO LIVING SUGAR CONTROL CAPSULES, 90 CAPSULES, Product No. Ue82004, UPC Code 097467820043, Lots 1361754, BBE 10/2025 and 1364325, BBE 10/2025
Consumers who may have purchased affected lots of NaturesPlus Keto Living Sugar Control Capsules are advised to return them to the place of purchase. No other Natural Organics, Inc. products are affected by this recall. Natural Organics, Inc. has removed all affected products within existing inventory.
This voluntary recall is announced in accord with FDA guidelines. We are initiating recall notices to our accounts and consumers who received inventory of the recalled products with instructions for returning the recalled products and for notifying their customers of the recall. Consumers with questions may contact the company Monday – Friday, from 8:00 am to 4:30pm EDT.
Company name: NATURAL ORGANICS, INC
Brand name: NaturesPlus
Product recalled: Keto Living Sugar Control Capsules
Reason of the recall: Undeclared Gluten
FDA Recall date: May 06, 2022
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