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ELV Alipotec Mexican Tejocte Root Supplement - recalled due to the presence of yellow oleander, USA

3 months ago source www.fda.gov

Recall notice

United States

WORLD GREEN NUTRITION, INC. is recalling ELV ALIPOTEC brand MEXICAN TEJOCOTE ROOT SUPPLEMENT PIECES (RAIZ DE TEJOCOTE MEXICANO SUPLEMENTO EN TROZOS), NET. WT, 0.3 0Z (7g), due to the presence of yellow oleander in this product. The consumption of yellow oleander can cause adverse effects on neurological, gastrointestinal, and cardiovascular health that can be serious or even fatal. Symptoms may include nausea, vomiting, dizziness, diarrhea, abdominal pain, heart changes, arrhythmia, and more. The product MEXICAN TEJOCOTE ROOT SUPPLEMENT PIECES, NET. WT, 0.3 0Z (7g) which is being recalled from the market is only sold through authorized distributors and not through e-commerce platforms or in physical stores. To date, this company has not received reports of illnesses related to the consumption of this product.

For easier identification of the product in question, it is noted that it comes in a white polyethylene container; green polypropylene lid; heat-shrinkable PET-G material label, authenticity hologram and net weight of 0.3 OZ (7g) and marked with the batch and expiration date mentioned below.

It is important to consider the above, since there are various products on the market that do not correspond to those marketed by this company, nor to the ELV ALIPOTEC brand.

Affected products:

- LOT: 090222, Expiration Date: 110424; - LOT: 250123, Expiration Date: 32328
- LOT: 070722, Expiration Date: 110424; - LOT: 250123, Expiration Date: 32428
- LOT: 150722N, Expiration Date: 120724; - LOT: 250123, Expiration Date: 32728
- LOT: 190722N, Expiration Date: 120724; - LOT: 250123, Expiration Date: 32828
- LOT: 150722N-1, Expiration Date: 120724; - LOT: 150722N, Expiration Date: 32828
- LOT: 110522, Expiration Date: 120724; - LOT: 160622, Expiration Date: 41928
- LOT: 070722, Expiration Date: 120724; - LOT: 260123D, Expiration Date: 41928
- LOT: 040722, Expiration Date: 120724; - LOT: 190722N, Expiration Date: 41928
- LOT: 260522, Expiration Date: 120724; - LOT: 250123, Expiration Date: 41828
- LOT: 190722N-1, Expiration Date: 120724; - LOT: 140223, Expiration Date: 51228
- LOT: 150822, Expiration Date: 120724; - LOT: 030223, Expiration Date: 51228
- LOT: 160622, Expiration Date: 92324; - LOT: 010323, Expiration Date: 51528
- LOT: 030123, Expiration Date: 030728; - LOT: 190722N, Expiration Date: 51528
- LOT: 150722N, Expiration Date: 030828; - LOT: 200722, Expiration Date: 51228
- LOT: 030123, Expiration Date: 030628; - LOT: 250123, Expiration Date: 51228
- LOT: 291122, Expiration Date: 030628; - LOT: 150722N, Expiration Date: 51228
- LOT: 250123, Expiration Date: 030628; - LOT: 020323, Expiration Date: 52328
- LOT: 130123, Expiration Date: 030728; - LOT: 260123D, Expiration Date: 52328
- LOT: 040722, Expiration Date: 031328; - LOT: 190722N, Expiration Date: 52428
- LOT: 030123, Expiration Date: 031328; - LOT: 260123D, Expiration Date: 71828
- LOT: 160622, Expiration Date: 031428; - LOT: 010323, Expiration Date: 71928
- LOT: 250123, Expiration Date: 031428; - LOT: 030223, Expiration Date: 71928
- LOT: 250123, Expiration Date: 031528; - LOT: 260123D, Expiration Date: 73128
- LOT: 250123, Expiration Date: 032128; - LOT: 260123D, Expiration Date: 80228
- LOT: 250123, Expiration Date: 032228; - LOT: 140223D, Expiration Date: 81528

The recall from the market began after the Food and Drug Administration issued the safety alert with the title “FDA Issues Warning About Certain Tejocote Root Supplements Substituted with Toxic Yellow Oleander”.

Additionally, it is reported that the marketing of the product in the United States of America is definitively suspended, discontinuing the product.

Consumers who have purchased the recalled lots of ELV ALIPOTEC MEXICAN TEJOCOTE ROOT SUPPLEMENT PIECES, NET. WT, 0.3 0Z (7g) to return them to the place where they made their purchase to obtain an exchange for another product marketed by the company.

If you are experiencing symptoms after eating this product 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 attention.

Company name: World Green Nutrition, Inc.
Brand name: ELV Alipotec
Product recalled: Mexican Tejocte Root Supplement
Reason of the recall: Product contains yellow oleander.
FDA Recall date: January 12, 2024

Source: www.fda.gov

#recall #us

Recent Interesting Reports

Aruba Aloe Balm N.V. is voluntarily recalling 40 lots of Aruba Aloe Hand Sanitizer Gel Alcohol 80% and Aruba Aloe Alcoholada Gel to the consumer level. The products have been found to contain alcohol denatured with methanol. Products were distributed between 5/1/2021 and 10/27/2023 and sold in … See More
the US online only via the Aruba Aloe Balm N.V. website. To date, Aruba Aloe Balm N.V. has not received any reports of adverse events related to these products.

Aruba Aloe Hand Sanitizer Gel is used as a sanitizer to help reduce bacteria that potentially can cause disease and is packaged in 12 fl oz (355 mL) dark green plastic bottles with white label reading in part “ARUBA ALOE Hand Sanitizer GEL 80% Alcohol Made in Aruba World’s Finest Aloe”, with barcode 0 82252 03300 5.

Aruba Aloe Alcoholada Gel is used for temporary relief of pain and itching associated with minor burns, sunburn, insect bites, or minor skin irritations and is packaged in two sizes: 2.2 fl oz (65 mL) plastic bottles with barcode 0 82252 34030 1 and 8.5 fl oz (251 mL) plastic bottles with barcode 0 82252 03120 9. The plastic bottles are transparent with a label reading in part “Alcoholada Gel Pain Relieving Gel 0.5% Lidocaine Hydrochloride”.

The affected Aruba Aloe Hand Sanitizer GEL product lots (filled in 12, 2.2, and 8.5 fl. oz bottles bottles) can be viewed in the link below.

Aruba Aloe Balm N.V. has notified all customers that bought these products by email and has offered a discount coupon for a next purchase. Consumers that have products which are being recalled should stop using and discard the product.

Risk Statement: Substantial methanol exposure can result in nausea, vomiting, headache blurred vision, coma, seizures, permanent blindness, permanent damage to the central nervous system, or death. Although all persons using these products on their hands are at risk, young children who accidently ingest these products and adolescents and adults who drink these products as an alcohol (ethanol) substitute are most at risk for methanol poisoning.

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: Aruba Aloe Balm N.V.
Brand name: Aruba Aloe
Product recalled: Hand Sanitizer Gel and Alcoholada Gel
Reason of the recall: Product contains methanol
FDA Recall date: April 05, 2024

Source: www.fda.gov
See Less

#recall #us

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SlimFit Fusion Keto+ ACV Gummies, Moorpark, CA, USA

2 weeks ago reported by user-nghh4267

I received the SlimFit Fusion KETO+ ACV Gummies in the mail from DP 192-01 Northern Blvd Flushing NY 11358
I do not remember ordering and was charged 149.99. My back was unable to provide more information so I have no way of calling to return it. WTF am I to do?

#unorderedpackage #ketogummiesscam #delivery #moorpark #california #us

Last 30 days