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Dietary Supplements

Updated:

ForeverMen Natural Energy Boost - recalled due to undeclared allergens, USA

1 month ago •source www.fda.gov

Recall notice

FAonline INC, is voluntarily recalling all lots within expiry of the ForeverMen capsules to the consumer level. FDA analysis founds these products to be tainted with sildenafil and Tadalafil. Sildenafil/Tadalafil is an FDA approved drug for the treatment of erectile dysfunction, the presence of sildenafil in the … See More

#dietarysupplements #allergicreaction #recall #us #allergen

ForeverMen Natural Energy Boost - recalled due to undeclared allergens photo #1
303

Alipotec King Alipotec Raiz de Tejocote - recalled due toYellow oleander, USA

2 months ago •source www.fda.gov

Recall notice

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

#recall #dietarysupplements #amazon #us

Alipotec King Alipotec Raiz de Tejocote - recalled due toYellow oleander photo #1
303

H&Natural Brand Products - recalled due to Yellow oleander, USA

2 months ago •source www.fda.gov

Recall notice

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

#recall #dietarysupplements #walmart #amazon #us

H&Natural Brand Products - recalled due to Yellow oleander photo #1
303

Nordic Naturals Baby’s Vitamin D3 - recalled due to Elevated level of Vitamin D3 dosage, USA

2 months ago •source www.fda.gov

Recall notice

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

#recall #dietarysupplements #us

Nordic Naturals Baby’s Vitamin D3 - recalled due to Elevated level of Vitamin D3 dosage photo #1
303
Z

Reaction to Spring Valley liquid Biotin and Collagen, Chillicothe, OH, USA

3 months ago •reported by user-ztqzf923

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

#allergicreaction #dietarysupplements #chillicothe #ohio #us #cream

51

Spring Valley Biotin & Collagen Liquid Natural Berry Flavor Dietary Supplement - recalled due to potential mold contamination, USA

3 months ago •source www.accessdata.fda.gov

Recall notice

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

#recall #dietarysupplements #us

Spring Valley Biotin & Collagen Liquid Natural Berry Flavor Dietary Supplement - recalled due to potential mold contamination photo #1
303

Noah’s Wholesale, LLC Dietary Supplement - recalled due to undeclared Sildenafil, USA

5 months ago •source www.fda.gov

Recall notice

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

#dietarysupplements #recall #drugs #us

Noah’s Wholesale, LLC Dietary Supplement - recalled due to undeclared Sildenafil photo #1
303

Dr. Ergin’s SugarMD Advanced Glucose Support, Dietary Supplement - recalled due to undeclared Glyburide and Metformin, USA

5 months ago •source www.fda.gov

Recall notice

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

#recall #amazon #dietarysupplements #us

Dr. Ergin’s SugarMD Advanced Glucose Support, Dietary Supplement - recalled due to undeclared Glyburide and Metformin photo #1
303

Botanical-Be Dietary Supplements - recalled due to Undeclared Diclofenac, USA

6 months ago •source www.fda.gov

Recall notice

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

#drugs #recall #dietarysupplements #us

Botanical-Be Dietary Supplements - recalled due to Undeclared Diclofenac photo #1
303

Bacaolinita - recalled due to Unapproved PEG-40 Hydrogenated Castor Oil, USA

10 months ago •source www.fda.gov

Recall notice

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

#recall #dietarysupplements #us

Bacaolinita - recalled due to Unapproved PEG-40 Hydrogenated Castor Oil photo #1
303

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