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Ridley Block Operations 12% Protein Sheep feed - recalled due to Elevated levels of copper, USA

3 years ago

United States

Company name: Ridley Block Operations
Brand name: Ultralyx
Product recalled: 12% Protein Sheep feed
Reason of the recall: Elevated levels of copper
FDA Recall date: July 13, 2020
Recall details: No other products are affected Ridley Block Operations is voluntarily recalling Ultralyx® 12% Protein Sheep with batch number HB01679401. The product has been found to contain elevated levels of copper. With prolonged consumption, the affected product could potentially have adverse health effects on sheep, including reductions in daily gains, icterus, partially cirrhotic livers and hemoglobin-stained kidneys. Occasionally, death occurs in copper-toxic sheep.

This recall relates only to Ultralyx 12% Protein Sheep with the following batch numbers printed on the package:

- Product Name: Ultralyx 12% Protein Sheep
- Batch/Lot# : HB01679401
- Item No./Product No.: 24419
- Package Info.: 50# Block

Customers are asked to remove all product matching this batch number from distribution and inventory and discontinue feeding it immediately.

No other batch number or other Ridley Block Operations products are involved in this voluntary recall. Of the batch of twenty blocks included in the recall, two blocks remain in the marketplace.

Ridley Block Operations will continue to work closely with the Food and Drug Administration throughout the recall process. Our representatives are in direct communication with our customers to ensure the proper identification and removal of the impacted products.

Check the full recall details on fda.gov

Source: FDA

303


Related Reports

A previous version of this press release was issued on 12/22/2023. This press release was updated to include all states that may have received the recalled product lot numbers.

Blue Ridge Beef is expanding their recall to include additional lot numbers due to contamination of Salmonella and... See More Listeria monocytogenes. The products were distributed between 11/14/2023 – 12/20/2023. These products were packaged in clear plastic and sold primarily in retail stores located in the states of: CT, FL, IA, IL, MA, MD, MI, NC, NY, OH, OR, PA, RI, TN, VA & WI. No illnesses have been reported to date.

Salmonella and Listeria monocytogenes can affect animals eating the products and there is risk to humans from handling contaminated pet products, especially if they have not thoroughly washed their hands after having contact with the products or any surfaces exposed to these products.

Healthy people infected with Salmonella should monitor themselves for some or all of the following symptoms: nausea, vomiting, diarrhea or bloody diarrhea, abdominal cramping and fever. Rarely, Salmonella can result in more serious ailments, including arterial infections, endocarditis, arthritis, muscle pain, eye irritation, and urinary tract symptoms. Consumers exhibiting these signs after having contact with this product should contact their healthcare providers.

Pets with Salmonella and Listeria infections may be lethargic and have diarrhea or bloody diarrhea, fever, and vomiting. Some pets will have only decreased appetite, fever, and abdominal pain. Infected but otherwise healthy pets can be carriers and infect other animals or humans. If your pet has consumed the recalled product and has these symptoms, please contact your veterinarian.

On 12/15/2023 the firm was notified by the North Carolina Department of Agriculture and Consumer Services that one lot of each of the products were sampled and tested positive for Salmonella and Listeria monocytogenes. However, out of an abundance of caution the firm is recalling all lots with the used by dates between N24 1114 to N24 1224.

A list of the products is below:
- Product: Kitten Grind, Size: 2lbs, UPC: 8 54298 00101 6, All Lot #/Use By Dates Between: N24 1114 to N24 1224.
- Product: Kitten Mix, Size: 2lbs, UPC: 8 54298 00243 6, All Lot #/Use By Dates Between: N24 1114 to N24 1224.
- Product: Puppy Mix, Size: 2lbs, UPC: 8 54298 00169 6, All Lot #/Use By Dates Between: N24 1114 to N24 1224
The lot numbers and used by dates are located on the silver tabs at the end of the tubes.

Consumers who have purchased these products are urged to contact Blue Ridge Beef for a full refund and destroy the food in a way that children, pets, and wildlife cannot access.

Do not sell or donate the recalled products. Do not feed the recalled product to pets or any other animals. Wash and sanitize pet food bowls, cups, and storage containers. Always ensure you wash and sanitize your hands after handling recalled food or any utensils that come in contact with recalled food..

In case you are experiencing Salmonella and Listeria monocytogenes symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain, and diarrhea, it is important to report it. It can help to detect & resolve outbreaks early and prevent others from being harmed, and it enables better surveillance. If symptoms persist, seek medical care.

Company name: Blue Ridge Beef
Brand name: Blue Ridge Beef
Product recalled: Kitten Grind, Kitten Mix, and Puppy Mix
Reason of the recall: Potential contamination of Salmonella and Listeria monocytogenes
FDA Recall date: January 03, 2024

Source: fda.gov
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Merck Animal Health, known as MSD Animal Health outside of the United States and Canada, a division of Merck & Co., Inc., Rahway, N.J., USA. (NYSE:MRK), is voluntarily recalling three batches of BANAMINE®/BANAMINE®-S (flunixin meglumine injection) 50 mg/mL in the United States, used for injection in cattle,... See More swine and horses to the consumer level due to the presence of particulate matter. BANAMINE® /BANAMINE®-S (flunixin meglumine injection) is a prescription product in the U.S. To date, no adverse event reports have been received for the recalled batches.

Particulates were observed during routine quality testing and reviews for the following batches:
- BANAMINE 100mL, UIN 065474, NDC 00061-0851-03, Batch 2834102, exp Oct. 2024. Distribution dates: March 6, 2023, to May 3, 2023
- BANAMINE 250mL, UIN 065476, NDC 00061-0851-04, Batch 2864102, exp Nov. 2024. Distribution dates: June 21, 2023, to July 11, 2023
- BANAMINE-S 100mL, UIN 065477, NDC 0061-1838-30, Batch 2834103, exp Oct. 2024. Distribution dates: March 20, 2023, to May 16, 2023

The lot number (LOT) and expiry date (EXP) is located at the bottom right part of the bottle label.

The administration of an injectable product that contains particulate matter may result in local irritation, swelling or infection in response to the foreign material. After intravenous administration in large animals, such as cattle or horses, particulate matter could travel to the lungs which could result in local tissue damage.

Flunixin meglumine is a potent, non-narcotic, nonsteroidal, analgesic agent with anti-inflammatory and antipyretic activity. It is approved in the US only for intravenous use in beef and dairy cattle, for intravenous and intramuscular use in horses and for intramuscular use in swine.

Customers who have received the affected products should stop using them and refer to their recall letter for product return instructions. Merck Animal Health is working with our distributor partners to ensure that unused product is no longer in distribution or with customers.

Company name: Merck Animal Health
Brand name: Merck Animal Health
Product recalled: Banamine; Banamine-S
Reason of the recall: Potential presence of particulate matter
FDA Recall date: September 01, 2023

Source: fda.gov
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303


Nestlé Purina PetCare Company is expanding its voluntary recall of Purina Pro Plan Veterinary Diets EL Elemental (PPVD EL) prescription dry dog food due to a supplier error resulting in potentially elevated levels of vitamin D in two additional product lots, which precede the production dates of... See More the previously recalled lots. The original announcement was made on February 8, 2023. No other Purina pet care products are affected.

The expansion comes following an investigation prompted by Purina that uncovered new information about a production error from a U.S. supplier that was made only to this specific formula and resulted in potentially elevated levels of vitamin D. Vitamin D is an essential nutrient for dogs; however, ingestion of elevated levels can lead to health issues depending on the level of vitamin D and the length of exposure. Vitamin D toxicity may include vomiting, loss of appetite, increased thirst, increased urination, and excessive drooling to renal (kidney) dysfunction. A list of the additional impacted product is below. Bags of PPVD EL with the UPC Code and Production Code below should be immediately discarded.

Product: Purina Pro Plan Veterinary Diets EL Elemental (PPVD EL)
UPC Code (*First 8 characters equal to): 38100 19190 – 8 lb / Production Code: 2213 1082 (NEW)
UPC Code (*First 8 characters equal to): 38100 19192 – 20 lb / Production Code: 2214 1082 (NEW)

The affected dry dog food was distributed throughout the United States by prescription only through veterinary clinics, Purina Vet Direct, Purina for Professionals, and other select retailers with the ability to validate a prescription.

Pet owners who purchased bags of the product listed above are asked to immediately stop feeding and throw it away in a container where no other animals, including wildlife, can get to it. If signs such as weight loss, excessive drooling, vomiting, loss of appetite or increased thirst or urination have occurred in their dog while eating this diet, pet owners should contact their veterinarian.

Veterinary and other retail partners should remove and destroy the affected product from their inventory.

In case your pet experiences harm from these products, it is important to report it. It can help to detect & resolve issues and prevent others from being harmed, and it enables better surveillance.

Company name: Nestle Purina PetCare Company
Brand name: Purina
Product recalled: Pro Plan Veterinary Diets EL Elemental (PPVD EL) prescription dry dog food
Reason of the recall: Potential Elevated Ingredient Level
FDA Recall date: March 10, 2023

Source: fda.gov
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303


Stratford Care USA, Inc of Odessa, Florida is recalling multiple brands of Omega-3 Supplements for cats and dogs due to potentially elevated levels of Vitamin A. Vitamin A is an essential nutrient for dogs; however, ingestion of elevated levels can lead to health issues depending on the... See More level of Vitamin A and the length of exposure. Omega-3 Supplements for cats and dogs was distributed throughout the United States in Veterinary Clinics, Distribution Centers, Retail Stores, and Online Market Places such as Amazon and Chewy.

Vitamin A toxicity may include general malaise, anorexia, nausea, peeling skin, weakness, tremors, convulsions, paralysis, and death. Stratford Care USA, Inc is taking this action after receiving a single Serious Adverse Event from a sole consumer regarding their dogs’ exhibiting signs of Vitamin A toxicity after consuming the supplement. This is the only Adverse Event to date.

Currently, Stratford Care USA, Inc in collaboration with the FDA is removing all products with these lot numbers from the market. No other Stratford Care USA, Inc products are affected. The white plastic container containing 60 soft gels has the marking on the bottom of the container that states “lot 31133 EXP 04/13/23” and “lot 30837 EXP 10/26/22”, this product has been private labeled under various brand names.

Affected products:
- Brand Name: All Creatures Animal Hospital. Product Name: Omega-V3 Softgels. UPC (If Applicable): NA.
- Brand Name: All Veterinary Supply, INC. Product Name: Omega-V3 Softgels. UPC (If Applicable): NA.
- Brand Name: Jungle Pet. Product Name: Skin+Coat Omega-3 Soft Gels. UPC (If Applicable): 85000395223.
- Brand Name: Animal Medical Clinic. Product Name: Omega V3 Softgels. UPC (If Applicable): 169682510808.
- Brand Name: Animal Medical Clinic Melbourne Beach. Product Name: Omega V3 Softgels. UPC (If Applicable): .
- Brand Name: Animal Care Hospital. Product Name: Omega-3 Fatty Acid Max Strength Soft Gels. UPC (If Applicable): NA.
- Brand Name: Animal Medical Center. Product Name: Omega-V3 Softgels. UPC (If Applicable): NA.
- Brand Name: Barnes Animal Hospital. Product Name: Omega-V3 Softgels. UPC (If Applicable): NA.
- Brand Name: Brentwood Animal Hospital. Product Name: Omega-V3 Softgels. UPC (If Applicable): NA.
- Brand Name: Cherokee Trail Veterinary Hospital. Product Name: Omega-V3 Softgels. UPC (If Applicable): NA.
- Brand Name: Clinton Animal Hospital. Product Name: Omega-V3 Softgels. UPC (If Applicable): NA.
- Brand Name: Clyde’s Animal Clinic. Product Name: Omega-V3 Softgels. UPC (If Applicable): NA.
- Brand Name: Coastal Animal Clinic. Product Name: Omega-V3 Softgels. UPC (If Applicable): NA.
- Brand Name: Columbia Hospital For Animals. Product Name: Omega-V3 Softgels. UPC (If Applicable): NA.
- Brand Name: Compassion Veterinary Clinic. Product Name: Omega-V3 Softgels. UPC (If Applicable): NA.
- Brand Name: Doc Ladue’s. Product Name: Omega-V3 Softgels. UPC (If Applicable): NA.
- Brand Name: Dogwood Veterinary Hospital. Product Name: Omega-V3 Softgels. UPC (If Applicable): NA.
- Brand Name: Doral Centre Animal Hospital. Product Name: Omega-V3 Softgels. UPC (If Applicable): NA.
- Brand Name: Eagles Landing Veterinary Hospital. Product Name: Omega-V3 Softgels. UPC (If Applicable): NA.
- Brand Name: Pet Health Solutions. Product Name: Omega Caps. UPC (If Applicable): 814087005489.
- Brand Name: SPCA of North Brevard. Product Name: Omega-V3 Soft Gels. UPC (If Applicable): .
- Brand Name: LaVale Veterinary Hospital. Product Name: Omega-V3 Soft Gels. UPC (If Applicable): NA.
- Brand Name: Twin Maples. Product Name: Omega-V3 Soft Gels. UPC (If Applicable): NA.
- Brand Name: University Animal Hospital. Product Name: Omega-V3 Soft Gels. UPC (If Applicable): NA.
- Brand Name: Venice Pines Veterinary Clinic. Product Name: Omega-V3 Soft Gels. UPC (If Applicable): NA.
- Brand Name: Lake Dow Animal Hospital. Product Name: Omega-V3 Soft Gels. UPC (If Applicable): NA.
- Brand Name: MVH Mann Veterinary Hospital. Product Name: Omega-V3 Soft Gels. UPC (If Applicable): NA.
- Brand Name: All Paws Animal Clinic Royal Palm Beach. Product Name: Omega-V3 Soft Gels. UPC (If Applicable): NA.
- Brand Name: Bottle Tree Animal Hospital. Product Name: Omega-V3 Soft Gels. UPC (If Applicable): NA.
- Brand Name: Brookwood Veterinary Clinic. Product Name: Omega-V3 Soft Gels. UPC (If Applicable): NA.
- Brand Name: Cleveland Park Animal Hospital. Product Name: Omega-V3 Soft Gels. UPC (If Applicable): NA.
- Brand Name: Crown Heights Animal Hospital. Product Name: Omega-V3 Softgels. UPC (If Applicable): NA.
- Brand Name: Eagle’s Landing Veterinary Hospital. Product Name: Omega-V3 Softgels. UPC (If Applicable): NA.
- Brand Name: LVH Veterinary. Product Name: Omega-V3 Softgels. UPC (If Applicable): NA.
- Brand Name: Mt Orab Veterinary Clinic. Product Name: Dr. Hayes’s Omega-V3 Soft Gels. UPC (If Applicable): NA.
- Brand Name: Oak Tree Animal Hospital. Product Name: Omega-V3 Softgels. UPC (If Applicable): NA.
- Brand Name: Patterson Veterinary Hospital – Mason. Product Name: Omega-V3 Softgels. UPC (If Applicable): NA.
- Brand Name: Prospect Heights Animal Hospital. Product Name: Omega-V3 Softgels. UPC (If Applicable): NA.
- Brand Name: Smyth County Animal Hospital. Product Name: Omega-V3 Softgels. UPC (If Applicable): NA.
- Brand Name: Stateline Animal Clinic. Product Name: Omega-V3 Softgels. UPC (If Applicable): NA.
- Brand Name: The Pet Clinic of Urbana, LLC. Product Name: Omega-V3 Softgel. UPC (If Applicable): NA.
- Brand Name: Valdosta Animal Hospital. Product Name: Omega-V3 Softgels. UPC (If Applicable): NA.
- Brand Name: Viking Community Animal Hospital. Product Name: Omega-V3 Softgels. UPC (If Applicable): NA.
- Brand Name: Westbrook Animal Hospital. Product Name: Omega-V3 Softgels. UPC (If Applicable): NA.
- Brand Name: My Pet Hospital. Product Name: Omega-3 Soft Gels. UPC (If Applicable): NA.
- Brand Name: North Shore Animal League America. Product Name: Omega-V3 Softgels. UPC (If Applicable): NA.
- Brand Name: NPC Northgate Pet Clinic. Product Name: Omega-V3 Softgels. UPC (If Applicable): NA.
- Brand Name: Northwest Tennessee Veterinary Services. Product Name: Omega-V3 Softgels. UPC (If Applicable): NA.
- Brand Name: Pawstruck.com. Product Name: Omega-V3 Soft Gels. UPC (If Applicable): 850005963080.
- Brand Name: Perry Animal Clinic. Product Name: Omega-V3 Softgels. UPC (If Applicable): NA.
- Brand Name: Pleasant Plains Animal Hospital. Product Name: Omega-V3 Softgels. UPC (If Applicable): NA.
- Brand Name: Seiler Animal Hospital. Product Name: Omega-V3 Softgels. UPC (If Applicable): NA.
- Brand Name: Stratford Animal Health. Product Name: Omega-V3 Softgels. UPC (If Applicable): NA.
- Brand Name: Summerfields Animal Hospital. Product Name: Omega-V3 Softgels. UPC (If Applicable): NA.
- Brand Name: SensoVet Animal Health Wellness. Product Name: Advanced Omega-3 Softgel. UPC (If Applicable): NA.
- Brand Name: University Animal Hospital. Product Name: Omega-V3 Softgels\. UPC (If Applicable): NA.
- Brand Name: Vet4Bulldog. Product Name: V4B Bully Fish oil omega-3 EFA. UPC (If Applicable): 603981565911.
- Brand Name: Waggin’ Wheel Vet Clinic. Product Name: Omega-V3 Softgels. UPC (If Applicable): NA.
- Brand Name: Wellsboro Small Animal Hospital Veterinary Medical Center. Product Name: Omega-V3 Softgels. UPC (If Applicable): NA.
- Brand Name: Wickham Road Animal Hospital. Product Name: Omega-V3 Softgels. UPC (If Applicable): NA.
- Brand Name: Wilton Manors Animal Hospital. Product Name: Omega-V3 Softgels. UPC (If Applicable): NA.

In case your pet experiences harm from these products, it is important to report it. It can help to detect & resolve issues and prevent others from being harmed, and it enables better surveillance.

Company name: Stratford Care USA, Inc
Brand name: Multiple brands
Product recalled: Omega-3 Supplements for cats and dogs
Reason of the recall: Potential elevated levels of Vitamin A
FDA Recall date: March 10, 2023

Source: fda.gov
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303


Vet intentionally mishandled animal while it was under anesthesia and permanently damaged its hip. See Less
963


Columbia REA is reporting a power outage that impacted about 100 customers on Wednesday, March 27. At about 3:30 p.m. The company said on Facebook that most of the power has been restored, except for the area around Highway 125 and Commercial Drive.

Outage link: columbiarea.coop
Source:... See More union-bulletin.com
Published: 2024-03-27
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On Wednesday 27th, the boil advisory is issued for customers from Cornerstone Market to Ruby Lane on Hwy 157.

Source: discoverdade.com
Published: 2024-03-27 See Less


Residents of Fore Acres, Hillside Acres and Courtney Acres should boil water they use for drinking, cooking, and brushing teeth, Marion County Utilities announced Wednesday 27th. The public utility issued a precautionary boil water notice Wednesday because of a water main repair.

Source: mynews13.com
Published: 2024-03-27 See Less


An Adair County rural water district says it is now safe to drink water again without having to boil it. The state Department of Environmental Quality had placed a boil order for rural district two customers after finding e-coli in the system.

Source: news9.com
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A boil order is in effect for parts of New Boston until further notice due to a water main break. The affected areas are from Clay Street to Franklin and from Linden to Broadway.

Source: wrmj.com
Published: 2024-03-27 See Less


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On March 1, 2024, Sleepnet Corporation initiated a worldwide recall for all CPAP and BIPAP masks with magnets due to potential interference with certain medical devices. When a magnet comes into close proximity to certain medical implants or metallic implants, it could interfere with the performance or... See More the position of the implant, potentially resulting in serious injury or death. Sleepnet has been distributing masks with magnets worldwide since 2006 and to date, there have been no Medical Device Reports associated with the Sleepnet masks with magnets.

Affected products are Mojo Full Face Vented Mask, Mojo Full Face Non‐Vented Mask, Mojo 2 Full Face Vented Mask, Mojo 2 Full Face Non‐ Vented Mask, Mojo 2 Full Face AAV Non‐Vented Mask, iQ 2 Nasal Mask, and Phantom 2 Nasal Mask. This is applicable to all lot/UDI numbers.

Sleepnet masks with magnets are safe when used in accordance with the newly updated Instructions for Use. Continue using masks according to the updated instructions and labeling if patients or people in close proximity to them do not have implanted metallic medical devices or metallic objects in the body.

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1- New Contraindication:
Do not use this mask if you or anyone (example: household members, bed partners, caregivers, etc.) in close physical contact with your mask has an active medical implant or metallic implant that will interact with magnets. Implant examples include, but are not limited to, pacemakers, implantable cardioverter defibrillators (ICD), neurostimulators, aneurysm clips, metallic stents, ocular implants, insulin/infusion pumps, cerebral spinal fluid (CSF) shunts, embolic coils, metallic splinter, implants to restore hearing or balance with implanted magnets (such as cochlear implants), flow disruption devices, contact lenses with metal, dental implants, metallic cranial plates, screws, burr hole covers, bone substitute device, magnetic metallic implants/electrodes/valves placed in upper limbs , torso, or higher, etc. If you have any questions regarding the implant, consult your physician or the manufacturer of your implant.

2- Updated Warning:
Magnets are used in the mask and headgear clips with a field strength of 380mT. With the exception of the devices identified in the contraindication, ensure that the mask is kept at least 6 inches (approx. 16 cm) away from any other medical implants or medical devices that can be impacted by the magnetic fields to avoid possible effects from localized magnetic fields. This applies to you or anyone in close physical contact with your mask.

If a patient, or anyone in close physical contact, has an active medical implant or metallic implant, they should contact their mask supplier to find a replacement mask that does not include magnets. If the patient is unsure whether or not they should use the mask, they should consult their physician or the manufacturer of their implant.

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: Sleepnet Corporation
Brand name: Mojo, Mojo 2, iQ 2, Phantom 2
Product recalled: CPAP and BIPAP Masks with Magnets
Reason of the recall: Potential interference with certain medical implants
FDA Recall date: March 18, 2024

Source: fda.gov
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