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A bottle of SUBGENIX, Ewa Beach, HI, USA
2 months ago
Ewa Beach, Hawaii, United States
I DID NOT ORDER THIS BOTTLE THAT WAS SENT TO ME!! WHAT IS THIS??
248
OV
anonymous35271
I received this product via ups today 09/13/2023. I did not order this product sent by Fulfillment Center. I know it is some type of scam because I am 77 years old and would never order. I gave up that dream about 10 years ago.
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Recent Interesting Reports
LEADER OTC Ophthalmic Sterile Drops - recalled due to Insanitary manufacturing conditions, USA
4 weeks ago
Cardinal Health, Inc. is initiating a voluntarily recall for all lots of ophthalmic products supplied by Velocity Pharma, LLC to the consumer level. Cardinal Health, Inc. received information from FDA indicating investigators found insanitary conditions in the manufacturing facility and positive bacterial test results from environmental sampling... See More of critical drug production areas in the facility. Products were distributed Nationwide to Wholesalers and Retailers starting December 12, 2021. To date, Cardinal Health, Inc., and its subsidiaries have received reports of three (3) adverse events related to these products. The reports of adverse events were shared with their supplier, Velocity Pharma, LLC.
The recalled products are:
- LEADER™ Eye Irritation Relief (Polyvinyl Alcohol, 0.5%, Povidone, 0.6%, and Tetrahydrozoline Hydrochloride, 0.05%), 0.5 FL OZ bottle (15 mL), NDC:
- LEADER™ Dry Eye Relief (Carboxymethylcellulose Sodium, 1%), 0.5 FL OZ bottle (15 mL), NDC: 70000-0089-1
- LEADER™ Lubricant Eye Drops (Carboxymethylcellulose Sodium, 0.5%), 0.5 FL OZ bottle (15 mL). NDC: 70000-0090-1
- LEADER™ Lubricant Eye Drops (Carboxymethylcellulose Sodium, 0.5%), 2 bottles, 0.5 FL OZ (15 mL) each. NDC: 70000-0090-2 (Carton) 70000-0090-1 (Bottle)
- LEADER™ Dry Eye Relief (Polyethylene Glycol 400, 0.4% and Propylene Glycol, 0.3%), 0.33 FL OZ bottle (10 mL), NDC: 70000-0088-1
- LEADER™ Lubricant Eye Drops (Propylene Glycol, 0.6%) 0.33 FL OZ bottle (10 mL), NDC:70000-0587-1
These products are available as over the counter (OTC) products used for temporary relief of burning and irritation due to dryness of the eye, for use as a protectant against further irritation or to relieve dryness of the eye, and/or to relieve redness of the eye due to minor eye irritations.
Risk Statement: For those patients who use these products, there is a potential risk of eye infections that could result in partial vision loss or blindness. These products are intended to be sterile. Ophthalmic drug products pose a potential heightened risk of harm to users because drug applied to the eyes bypass some of the body’s natural defenses.
Wholesalers, Distributors and Retailers that have the affected product which is being recalled should cease distribution of the products. Consumers should stop using the recalled eye drop products and may return them to the place of purchase.
In case you experience 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. If symptoms persist, seek medical care.
Company name: Cardinal Health, Inc.
Brand name: LEADER
Product recalled: OTC Ophthalmic Sterile Drops
Reason of the recall: Insanitary manufacturing conditions
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Received a package from "Jane" at 371 Little Falls Rd Unit 4 Cedar Grove, NJ. 07009. 2 "Trump" Coins - 1 "gold", 1 "silver". Never ordered anything from Jane and would NEVER order a Trump anything. See Less
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Insight Pharmaceuticals, a Prestige Consumer Healthcare Inc. company (“Insight”), is voluntarily recalling two lots of TING® 2% Miconazole Nitrate Athlete’s Foot Spray Antifungal Spray Powder to the consumer level. A recent review by our manufacturer and their third-party lab found that samples from two lots of the... See More product contained elevated levels of benzene. The affected lots were distributed nationwide in the United States through a limited number of retailers and online. To date, the Company has not received any serious adverse events related to this recall.
Risk Statement: Benzene is classified as a human carcinogen. Exposure to benzene can occur by inhalation, orally, and through the skin and it potentially can result in cancers including leukemia and blood cancer of the bone marrow and blood disorders which can be life-threatening. Insight is recalling these products out of an abundance of caution. Benzene is ubiquitous in the environment. Humans around the world have daily exposure to it indoors and outdoors from multiple sources.
TING® 2% Miconazole Nitrate Athlete’s Foot Spray Antifungal Spray Powder is packaged in green and white aerosol cans with Lot codes located on the bottom of the can.
Samples of the recalled lots below have been found to contain trace levels of Benzene related to the propellant that sprays the product out of the can. Benzene is not an ingredient in any Ting products.
Affected products:
- Product: TING 2% Miconazole Nitrate Athlete’s Foot Spray Antifungal Spray Powder, NDC: 63736-532-05, Lot Code: 0H88645, Expiration: 07/24, Package Size: 4.5 oz/128 g
- Product: TING 2% Miconazole Nitrate Athlete’s Foot Spray Antifungal Spray Powder, NDC: 63736-532-05, Lot Code: 0B88345, Expiration: 02/24, Package Size: 4.5 oz/128 g
Insight has notified retailers via overnight mail to remove any remaining recalled product from shelves and follow the instructions provided in the Drug Recall Notification. The company will also offer reimbursement for consumers who have purchased TING® 2% Miconazole Nitrate Athlete’s Foot Spray Antifungal Spray marked with one of the lot codes.
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: Insight Pharmaceuticals
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Reason for the recall: Presence of benzene
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This is what they sent, then wanted me to mail it back to them at my expense of $17.00, so it was sent but of course never received.
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