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Dietary Supplements

Updated: February 23, 2024 8:01 PM
Backstage Center is issuing a recall of approximately 280 Bottles of Alipotec Raiz de Tejocote, dietary supplements, that are labeled with the "Alipotec King" sticker. This recall is being initiated because FDA analysis found that the product contains toxic yellow oleander. The product has been exclusively distributed... See More on Amazon.com since September 15, 2023. There have been no reports of injury or illness, to date.

The recalled product, which contains yellow oleander instead of tejocote, may induce serious neurologic, gastrointestinal, and cardiovascular adverse health effects. Symptoms may be severe or fatal, including nausea, vomiting, dizziness, diarrhea, abdominal pain, cardiac dysrhythmia, and others. Immediate medical attention is advised for consumers experiencing such symptoms.

Product Name: Alipotec King, Alipotec Raiz de TejocoteContainer
Description: Cylindrical bottle with a green top, white body, and contains approximately 30 granules, weighing a total of 0.35oz.
Lot Codes: 238124
Expiration date: 08-2027
Total Distributed: 280 Bottles
Consumer Instructions: Consumers should immediately discontinue use of the product.

In case you experience harm from extraneous materials, 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: Backstage Center
Brand name: Alipotec King
Product recalled: Alipotec Raiz de Tejocote
Reason of the recall: Product contains yellow oleander, a poisonous plant
FDA Recall date: February 23, 2024

Source: fda.gov
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San Luis, AZ, G.A. Mart dba H&Natural, is voluntarily recalling 2 lots of H&NATURAL TejoRoot, 10g pills, and 2 lots of H&NATURAL Brazil Seed, .167g Seeds to the consumer level. The products have been found via random FDA testing to contain yellow oleander, a poisonous plant native... See More to Mexico and Central America. H&NATURAL TejoRoot and H&NATURAL Brazil Seed were distributed Nationwide to via internet on their site, Amazon.com, and Walmart.com. The company has received one report of gastrointestinal illness, including painful symptoms in conjunction with internal bleeding in connection with H&NATURAL TejoRoot, and has not received any reports of adverse events in connection with H&NATURAL Brazil Seed.

Risk Statement: Ingestion of yellow oleander can cause neurologic, gastrointestinal, and cardiovascular adverse health effects that may be severe, or even fatal. Symptoms may include nausea, vomiting, dizziness, diarrhea, abdominal pain, cardiac changes, dysrhythmia, and more.

The recalled dietary supplements can be identified by the H&NATURAL logo and the following descriptions:
- Tejo Root, Raiz de Tejocte, H&Natural, Healthy, and Natural, Dietary Supplement, 10g pills, is packaged in a box or bottle, with UPC (196852946921)
- Brazil Seed Pure Natural Semilla de Brasil, H& Natural, Healthy and Natural, 0.167g seeds, packaged in a box or bottle, with UPC (195893047529) (196852820641) (195893698721) (195893236893)(196852134618) (195893336975)

Recalled lots are labeled with the following expiration dates, 3/24 and 5/24.

Consumers that have the recalled H&NATURAL TejoRoot or H&NATURAL Brazil Seed lots should stop using the products. Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to taking or using this drug product.

In case you experience harm from extraneous materials, 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: G.A. Mart dba H&Natural
Brand name: H&Natural
Product recalled: Brazil Seed Pure Natural Semilla de Brasil & Tejo Root, Raiz de Tejocte
Reason of the recall: Product contains yellow oleander, a poisonous plant
FDA Recall date: February 23, 2024

Source: fda.gov
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Nordic Naturals is voluntarily recalling one lot of Nordic Naturals Baby’s Vitamin D3 Liquid. This recall is being conducted due to a manufacturing error that resulted in an elevated level of Vitamin D3 dosage or super potent dose. There have been no reports of adverse events to... See More date related to the use of this recalled product.

The recalled lot of Nordic Naturals Baby’s Vitamin D3 Liquid is 0.76 fl. oz. (22.5 mL), 400 IU (10mcg) D3. The affected lot number is 234909, with an expiration date of December 2025. The affected product is used as a dietary supplement for infants up to 12 months of age and is packaged in boxes containing one bottle and one dropper for dosage, under SKU RUS-02733. Approximately 3,800 units of product were affected, with one-fifth already returned by retailers.

Prolonged use of the recalled Baby’s Vitamin D3 Liquid could potentially lead to elevated vitamin D levels, resulting in vomiting, loss of appetite, increased thirst, frequent urination, and inability to thrive in infants.

Consumers, distributors, and retailers in possession of the recalled product should discontinue use immediately and return it to the place of purchase for a refund or replacement. The lot number can be found on the back of the box and on the bottle.

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: Nordic Naturals
Brand name: Nordic Naturals
Product recalled: Baby’s Vitamin D3 Liquid
Reason of the recall: Elevated level of Vitamin D3 dosage
FDA Recall date: February 19, 2024

Source: fda.gov
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The last 3 weeks to a month I had uncontrollable itching. So badly that my itching would break the skin in many places and would bleed and seep but yet still would itch. I lived on Benedryl everyday for about 2.5 weeks most of the time that... See More would calm it down enough to tolerate it. A few times I also used anti itch cream as well. I had no idea what had changed in my life to cause this. And it's been almost 2 weeks since I finished my supplement and opened a new one. It wasn't until I went to buy another one for next month that I found out that they had been recalled for mold which I have a very bad allergy to so it now makes perfect sense as to why I was having this reaction. I also had two more in my cabinet just so that I wouldn't run out. I checked them today and they were on the recall list sadly. | Symptoms: Allergic Reaction, Itching See Less
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FDA announced the recall of 24,324 units of Spring Valley Biotin & Collagen Liquid Natural Berry Flavor Dietary Supplement by BioMylz Pvt. Ltd. due to potential mold contamination. This product was distributed to a distribution center in California and then further distributed to distribution centers and retail... See More stores nationwide.

The recalled product is:
- Spring Valley Biotin & Collagen Liquid, Natural Berry Flavor, 15000 mcg, Dietary Supplement 29 doses 1 fl oz (29mL) UPC: 194346065158 Packaged in a glass bottle in a paper carton. Codes: NSBS2301, NSBS2302, NSBS2303, NSBS2306, NSBS2308

This recall was initiated on 12/1/2023 and its status is ongoing. Do not consume, use, sell, serve, or distribute the recalled product.

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.

Source: accessdata.fda.gov
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Noah’s Wholesale, LLC is voluntarily recalling one lot of rock# 03032021, exp:12/2027, 1200 mg/capsule, to the consumer level. FDA analysis has found the product to be tainted with Sildenafil. The product was distributed locally through convenience stores and some island jobbers (small wholesale distributors to retail). Noah’s... See More Wholesale has not received any reports of adverse events related to this recall to date.

Sildenafil is an ingredient known as a Phosphodiesterase Inhibitor (PDE-5) found in FDA-approved products for the treatment of male erectile dysfunction. The presence of sildenafil in this product renders the rock an unapproved drug for which the safety and efficacy have not been established and, therefore, subject to recall.

Risk Statement: Consumption of products with undeclared sildenafil may interact with nitrates found in some prescription drugs (such as nitroglycerin) and may cause a significant drop in blood pressure that may be life-threatening. People with diabetes, high blood pressure, high cholesterol, or heart disease often take nitrates. Among the adult male population, who are most likely to use this product, adult males who use nitrates for cardiac conditions are most at risk.

The Rock is marketed as a dietary supplement for male sexual enhancement and is packaged as a single pill in a blister pack. It is labeled as ORIGINAL THE ROCK, Male sexual performance, with the following UPC 6 61799 95052 7. Distributed by: Steele Products, Hallandale, FL. The Rock affected lot is lot#03032021, Exp:12/2027. The product can be identified by the red and black lettering on a white-flat small cardboard package with one red capsule seen through a clear blister window.

Noah’s Wholesale is notifying its distributors and customers by phone, emails, and through their sales representative and is arranging for a full refund/credit of all recalled products. Consumers who have the recalled product should stop using the product and return it to the place of purchase or discard the product immediately. Distributors and retailers should stop selling the product and contact Noah’s Wholesale LLC for a refund process.

Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to taking or using this drug product.

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: Noah’s Wholesale, LLC
Brand name: Noah’s Wholesale, LLC
Product recalled: Dietary Supplement with undeclared Sildenafil
Reason of the recall: Undeclared drug, Sildenafil
FDA Recall date: November 21, 2023

Source: fda.gov
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SugarMDs, LLC is voluntarily recalling Lot: 22165-003 Advance Glucose Support Supplement in 60, 120 and 180 count bottles to the consumer level. FDA analysis has found the product to be tainted with glyburide and metformin. The product was distributed Nationwide in the US -through internet sales via... See More amazon and their website. To date, SugarMDs LLC has not received any reports of adverse events related to this recall.

Glyburide and Metformin are active ingredients found in several FDA-approved prescription drugs used to treat type 2 diabetes. Products containing glyburide and metformin cannot be marketed as dietary supplements. Advanced Glucose Support Supplement is an unapproved new drug for which safety and efficacy have not been established and, therefore, subject to recall.

Risk Statement: Glyburide may pose serious and potentially life-threatening risks to consumers because this ingredient may result in unsafe drops in blood sugar levels (hypoglycemia). Common symptoms of hypoglycemia include fast heartbeat, shaking, sweating, nervousness or anxiety, irritability or confusion, dizziness, drowsiness, headache and hunger. Hypoglycemia may quickly become severe, resulting in seizures, coma or death. Metformin may pose a serious risk to consumers because this ingredient can cause a rare but serious side effect called lactic acidosis (a build-up of lactic acid in the blood) that can cause death if untreated. Symptoms of lactic acidosis include nausea, vomiting, fatigue, body aches, respiratory distress, abdominal pain and fast, deep breathing. Metformin may also cause hypoglycemia when taken together with other medications to lower blood sugar.

This tainted Advanced Glucose Support is marketed as a dietary supplement and is packaged in:
- 60 count bottle : UPC code 00195893927678 (UPC code located below the "Supplement Facts" panel)
- 120 count bottle: UPC code 00195893546978
- 180 count bottle: UPC code 00195893999576
An example product label can be found in the picture attached. The affected Advanced Glucose Support lots include the following: Lot# 22165-003 EXP: 09/2024

SugarMDs LLC is notifying its distributors and customers by email and is arranging for return of all recalled products. Consumers/distributors/retailers that have product which is being recalled should stop using and return to place of purchase for a full refund. Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to taking or using this drug product.

This recall is being conducted with the knowledge of the U.S. Food and Drug Administration.

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: SugarMDs, LLC
Brand name: Dr. Ergin’s
Product recalled: SugarMD Advanced Glucose Support, Dietary Supplement
Reason of the recall: Undeclared Glyburide and Metformin
FDA Recall date: November 15, 2023

Source: fda.gov
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Botanical-Be is voluntarily recalling all lots of Kuka Flex Forte, Capsules, Artri King, Capsules, and Reumo Flex, Capsules to the consumer level. FDA analysis has found these capsules, to be tainted with Diclofenac. Diclofenac is an approved non-steroidal anti-inflammatory drug (NSAID), the presence of Diclofenac in Kuka... See More Flex Forte, Artri King, and Reumo Flex renders them unapproved drugs for which safety and efficacy have not been established and, therefore, subject to recall. These products were distributed nationwide via the internet. To date, Botanical-Be has not received any reports of adverse events related to this recall.

These tainted products are marketed as a dietary supplement for relief of pain and inflammation associated with arthritis and are packaged as followed:
- Artri king distribute in the bottles with 100 capsules. Lot 35421, with an expiration date of December 19, 2025
- Kuka Flex distribute in the bottles with 30 capsules. All lots with an expiration date of December 12, 2024, and UPC code 0736640810265
- Reumo flex distribute in the boxes with 30 capsules. All lots with an expiration date of October 20, 2024.

Risk Statement: Consumption of undeclared diclofenac could result in serious adverse events that include cardiovascular, gastrointestinal, renal, and anaphylaxis in patients taking concomitant NSAIDs and/or anticoagulants, such as Warfarin, in those who have allergies to diclofenac, or those with underlying cardiovascular, gastrointestinal, renal, and hepatic illnesses.

Consumers in possession of these products should cease usage immediately and 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: Botanical-Be
Brand name: Multiple brands
Product recalled: Dietary Supplements with undeclared Diclofenac
Reason of the recall: Undeclared drug, Diclofenac
FDA Recall date: October 23, 2023

Source: fda.gov
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PROCAPS S.A. DE C.V. from San Salvador, El Salvador is voluntarily recalling Laboratorios Lopez's Bacaolinita 8 FL OZ, a dietary supplement, due to the label of the product not declaring, PEG-40 hydrogenated castor oil as an inactive ingredient on the labeling. Safety data on the oral ingestion... See More of PEG-40 hydrogenated castor oil in humans is scarce. Although rare, it has been published that PEG can interact with other medications and in sensitized individuals may cause hypersensitivity reactions, including anaphylaxis. This product was distributed to distributors in Delaware, Rhode Island, Texas, and California, and reached consumers through retail stores and online. It is important to highlight that, to date, no adverse events have been reported by consumers of Laboratorios Lopez's Bacaolinita 8 FL OZ, a dietary supplement.

Bacaolinita is marketed in a dark amber plastic 8 Fl Oz bottle packed in a cardboard box (UPC8-4152-0002-8). Affected lots and expiration dates are: 1358739 (EXP: 7/14/2023), 1379697 (EXP: 11/22/23), 1379718 (EXP: 11/22/23), 1397103 (EXP: 3/6/24), 1404273 (EXP: 4/19/24), 1416127 (EXP: 6/27/24), 1420872 (EXP: 7/26/24), 1423729 (EXP: 8/15 /24), 1451962 (EXP: 2/15/25).

Consumers who have purchased Bacaolinita are urged to return it to the place of purchase for a full refund.

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: PROCAPS S.A. DE C.V.
Brand name: Bacaolinita
Product recalled: Food and Beverage Safety/Unapproved Ingredient
Reason of the recall: Unapproved PEG-40 Hydrogenated Castor Oil
FDA Recall date: June 07, 2023

Source: fda.gov
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I received dietary supplements called "Manaplasfen Blood Sugar" and " Manaplasfen Keto Cleanse". I did not order these items which are evidently from a scam.
The package contains the 2 supplements and a pair ofr ear buds. I have tried to reach this company by using the... See More addtess on the package. What is the next step I can take. See Less
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