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Safety Reports: Drugs

Updated:

Real Time Reports

Regulatory Report

M Hand Sanitizer Alcohol Antiseptic 80% - recalled due to Contains Methanol and may be Sub-Potent for Ethanol, United States

5 years ago •source fda.gov • details

Company name: Medek, LLC
Brand name: M
Product recalled: M Hand Sanitizer Alcohol Antiseptic 80%
Reason of the recall: Contains Methanol and may be Sub-Potent for Ethanol
FDA Recall date: September 10, 2020
Recall details: Medek, LLC is voluntarily recalling all lots of M Hand Sanitizer Alcohol… See more

#handsanitizer #recall #drugs #unitedstates #sub

Consumer Safety Report M Hand Sanitizer Alcohol Antiseptic 80% - recalled due to Contains Methanol and may be Sub-Potent... photo #1
312   Comments Comment

Recall notice

Leafree Hand sanitizer - recalled due to Product is labeled as edible alcohol., United States

5 years ago •source fda.gov • details

Company name: CorgioMed LLC
Brand name: Leafree
Product recalled: Hand sanitizer
Reason of the recall: Product is labeled as edible alcohol.
FDA Recall date: September 03, 2020
Recall details: CorgioMed, LLC is voluntarily recalling all lots of Leafree Instant Hand Sanitizer-Aloe Vera, within expiry to the consumer… See more

#blood #handsanitizer #drugs #unitedstates #sugar

Recalls Leafree Hand sanitizer - recalled due to Product is labeled as edible alcohol. Company name: CorgioM... photo #1
312   Comments Comment

Recall notice

Nature-Throid and WP Thyroid - recalled due to Product may be sub potent, United States

5 years ago •source fda.gov • details

Company name: RLC Labs, Inc
Brand name: RLC Labs
Product recalled: Nature-Throid® and WP Thyroid®
Reason of the recall: Product may be sub potent
FDA Recall date: September 02, 2020
Recall details: RLC Labs, Inc. is voluntarily recalling a total of 483 lots of Nature-Throid® and WP… See more

#drugs #unitedstates #sub

Recalls Nature-Throid and WP Thyroid - recalled due to Product may be sub potent Company name: RLC Labs, In... photo #1
312   Comments Comment

Recall notice

bio aaa Hand Sanitizer - recalled due to Possible presence of methanol, Miami, FL, USA

5 years ago •source fda.gov • details

Company name: AJR Trading LLC
Brand name: bio aaa
Product recalled: Hand Sanitizer
Reason of the recall: Possible presence of methanol
FDA Recall date: September 03, 2020
Recall details: AJR Trading is voluntarily recalling 2,004 units of lot 20DF8307 of bio aaa Advance Hand Sanitizer currently in… See more

#handsanitizer #drugs #miami #florida #unitedstates

Recalls bio aaa Hand Sanitizer - recalled due to Possible presence of methanol Company name: AJR Trading LLC... photo #1
363   Comments Comment

Recall notice

Red-E male enhancement tablet - recalled due to Product contains undeclared sildenafil, USA

5 years ago •source fda.gov • details

Company name: The Protein Shoppe, LLC
Brand name: Red-E
Product recalled: Red-E male enhancement tablet
Reason of the recall: Product contains undeclared sildenafil
FDA Recall date: September 01, 2020
Recall details: Company Announcement The Protein Shoppe, LLC is voluntarily recalling all lots of “Red-E” (Male Enhancement tablet)… See more

#blood #drugs #unitedstates

Recalls Red-E male enhancement tablet - recalled due to Product contains undeclared sildenafil Company name:... photo #1
312   Comments Comment

Recall notice

Mylan N.V. Tranexamic Acid and Amiodarone HCl injections - recalled due to Vials potentially packaged in incorrect cartons, United States

5 years ago •source fda.gov • details

Company name: Mylan N.V.
Brand name: Mylan
Product recalled: Tranexamic Acid and Amiodarone HCl injections
Reason of the recall: Vials potentially packaged in incorrect cartons
FDA Recall date: August 31, 2020
Recall details: Mylan N.V. (NASDAQ: MYL) today announced that its U.S.-based Mylan Institutional LLC business is… See more

#blood #drugs #unitedstates

Recalls Mylan N.V. Tranexamic Acid and Amiodarone HCl injections - recalled due to Vials potentially package... photo #1
312   Comments Comment

Recall notice

Harmonic Nature Hand sanitizer - recalled due to Product contains 1 propanol, United States

5 years ago •source fda.gov • details

Company name: HARMONIC NATURE S. DE R.L. Mi
Brand name: Harmonic Nature
Product recalled: Hand sanitizer
Reason of the recall: Product contains 1 propanol
FDA Recall date: August 28, 2020
Recall details: Guadalupe, Nuevo Leon, Harmonic Nature is voluntarily recalling all 800 bottles Hand Sanitizer, 250mL, product… See more

#handsanitizer #drugs #unitedstates

312   Comments Comment

Recall notice

Zanilast+ Hand sanitizer - recalled due to Product contains 1-propanol., United States

5 years ago •source fda.gov • details

Company name: Nanomateriales, SA de CV
Brand name: Zanilast+
Product recalled: Hand sanitizer
Reason of the recall: Product contains 1-propanol.
FDA Recall date: August 26, 2020
Recall details: Apodaca, Nuevo Leon, Nanomateriales is voluntarily recalling all lots of ZANILAST+ GEL, Sanitizer gel, to the consumer level. FDA… See more

#handsanitizer #drugs #unitedstates

Recalls Zanilast+ Hand sanitizer - recalled due to Product contains 1-propanol. Company name: Nanomateriales... photo #1
312   Comments Comment

Recall notice

V-Klean, Medical Minded, Protz Hand Sanitizer - recalled due to Potential methanol (wood alcohol) presence and subpotent ethanol levels, USA

5 years ago •source fda.gov • details

Company name: Asiaticon SA de CV
Brand name: V-Klean, Medical Minded, Protz
Product recalled: Hand Sanitizer
Reason of the recall: Potential presence of methanol (wood alcohol) and subpotent ethanol levels
FDA Recall date: August 25, 2020
Recall details: Mexico City, Mexico, Asiaticon SA de CV (Mexico) is… See more

#handsanitizer #drugs #unitedstates

Recalls V-Klean, Medical Minded, Protz Hand Sanitizer - recalled due to Potential methanol (wood alcohol) p... photo #1
312   Comments Comment

Recall notice

Bayshore Pharmaceuticals, LLS Metformin Hydrochloride Extended-Release Tablets USP, 500 mg & 750 mg - recalled due to Due to the Detection of N-Nitrosodimethylamine (NDMA) Impurity, United States

5 years ago •source fda.gov • details

Company name: Bayshore Pharmaceuticals, LLS
Brand name: Bayshore Pharmaceuticals, LLS
Product recalled: Metformin Hydrochloride Extended-Release Tablets USP, 500 mg & 750 mg
Reason of the recall: Due to the Detection of N-Nitrosodimethylamine (NDMA) Impurity
FDA Recall date: August 20, 2020
Recall details: Company Announcement Bayshore Pharmaceuticals, LLC,… See more

#blood #drugs #unitedstates #sugar

Recalls Bayshore Pharmaceuticals, LLS Metformin Hydrochloride Extended-Release Tablets USP, 500 mg & 750 mg... photo #1
312   Comments Comment

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