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Safety Reports: Drugs

Updated:

Real Time Reports

Recall notice

Unauthorized novel CBD food supplements - recalled due to Unsafe Levels of THC, Ireland

4 years ago •source fsai.ie • details

The FSAI announced the recall of unauthorized novel CBD food supplements due to the presence of unsafe levels of delta‐9‐tetrahydrocannabinol (THC) based on the European Food Safety Authority (EFSA) acute reference dose.

The recalled products are:
- Jacob Hooy, 2.75%CBD+, 10 ml, Batch number: 060977-0302, Best before… See more

#cbd #drugs #recall #ireland

Recalls Unauthorized novel CBD food supplements - recalled due to Unsafe Levels of THC The FSAI announced th... photo #1
19   Comments Comment

Recall notice

Ruzurgi® 10 mg tablets - recalled due to Yeast, Mold, and Bacterial Contamination, USA

4 years ago •source fda.gov • details

Company name: Jacobus Pharmaceutical Company Inc.
Brand name: Ruzurgi®
Product recalled: Ruzurgi® (amifampridine) 10 mg tablets
Reason of the recall: Exceeds Specification for Total Yeast and Mold Counts
FDA Recall date: September 13, 2021
Recall details: Plainsboro, New Jersey, Jacobus Pharmaceutical Company Inc. is voluntarily recalling 3… See more

#recall #drugs #unitedstates

Recalls Ruzurgi® 10 mg tablets - recalled due to Yeast, Mold, and Bacterial Contamination Company name: Jaco... photo #1
313 1 Share   Comments Comment

Recall notice

Azurity Firvanq - recalled due to Product kit may contain incorrect diluent, USA

4 years ago •source fda.gov • details

Company name: Azurity Pharmaceuticals, Inc.
Brand name: Azurity
Product recalled: Firvanq
Reason of the recall: Product kit may contain incorrect diluent.
FDA Recall date: September 08, 2021
Recall details: Wilmington, MA, Azurity Pharmaceuticals, Inc. (“Azurity”) is voluntarily recalling one lot of Firvanq® (vancomycin hydrochloride for oral solution),… See more

#recall #drugs #unitedstates

Recalls Azurity Firvanq - recalled due to Product kit may contain incorrect diluent Company name: Azurity Ph... photo #1
312   Comments Comment

Recall notice

Hospira Aminosyn II, 15% - recalled due to visible particulate matter presence, USA

4 years ago •source fda.gov • details

Company name: ICU Medical, Inc.
Brand name: Hospira
Product recalled: Aminosyn II, 15%, An Amino Acid Injection, Sulfite
Reason of the recall: Presence of visible particulate matter
FDA Recall date: September 07, 2021
Recall details: ICU Medical, Inc. is voluntarily recalling one lot (2,112 units) of Aminosyn… See more

#blood #recall #drugs #unitedstates

Recalls Hospira Aminosyn II, 15% - recalled due to visible particulate matter presence Company name: ICU Med... photo #1
312   Comments Comment

Recall notice

Teligent Lidocaine HCl Topical Solution 4% - recalled due to Super potency, USA

4 years ago •source fda.gov • details

Company name: Teligent Pharma, Inc.
Brand name: Teligent
Product recalled: Lidocaine HCl Topical Solution 4%
Reason of the recall: Super potency
FDA Recall date: August 30, 2021
Recall details: Teligent Pharma, Inc. is voluntarily recalling one lot of Lidocaine HCl Topical Solution 4%, 50ml in a screw… See more

#recall #drugs #unitedstates

Recalls Teligent Lidocaine HCl Topical Solution 4% - recalled due to Super potency Company name: Teligent Ph... photo #1
312   Comments Comment

Recall notice

Pfizer Smoking cessation treatment - recalled due to high intake level content, USA

4 years ago •source fda.gov • details

Company name: Pfizer
Brand name: CHANTIX
Product recalled: Smoking cessation treatment
Reason of the recall: N-Nitroso Varenicline content above acceptable daily intake level
FDA Recall date: August 16, 2021
Recall details: Pfizer is voluntarily recalling an additional four lots of Chantix 0.5mg/1 mg Tablets to the patient… See more

#recall #pfizer #drugs #unitedstates

Recalls Pfizer Smoking cessation treatment - recalled due to high intake level content Company name: Pfizer... photo #1
312   Comments Comment

Recall notice

Sodium Bicarbonate in 5% Dextrose Injection 150mEq per 1,000 mL - recalled due to waterborne microbial contamination, USA

4 years ago •source fda.gov • details

Company name: SterRx, LLC
Brand name: SterRx, LLC
Product recalled: Sodium Bicarbonate in 5% Dextrose Injection 150mEq per 1,000 mL
Reason of the recall: Due to waterborne microbial contamination
FDA Recall date: August 10, 2021
Recall details: SterRx, LLC today announced the voluntary nationwide recall of three… See more

#recall #drugs #unitedstates

Recalls Sodium Bicarbonate in 5% Dextrose Injection 150mEq per 1,000 mL - recalled due to waterborne microb... photo #1
312   Comments Comment

Recall notice

Pfizer Smoking cessation treatment - recalled due to N-Nitroso Varenicline content above ADI level, USA

4 years ago •source fda.gov • details

Company name: Pfizer
Brand name: CHANTIX
Product recalled: Smoking cessation treatment
Reason of the recall: N-Nitroso Varenicline content above ADI level
FDA Recall date: July 19, 2021
Recall details: Pfizer is voluntarily recalling two lots of Chantix 0.5mg Tablets, two lots of Chantix 1 mg Tablets, and… See more

#pfizer #recall #drugs #unitedstates

Recalls Pfizer Smoking cessation treatment - recalled due to N-Nitroso Varenicline content above ADI level... photo #1
312   Comments Comment

Recall notice

NEUTROGENA and AVEENO aerosol Sunscreen - recalled due to presence of a carcinogen, USA

4 years ago •source fda.gov • details

Company name: Johnson& Johnson
Brand name: Neutrogena, Aveeno
Product recalled: Sunscreen
Reason of the recall: Testing identified low levels of benzene
FDA Recall date: July 14, 2021
Recall details: Johnson & Johnson Consumer Inc. (JJCI) is voluntarily recalling all lots of five NEUTROGENA® and AVEENO® aerosol sunscreen… See more

#johnsonjohnson #recall #drugs #unitedstates

Recalls NEUTROGENA and AVEENO aerosol Sunscreen - recalled due to presence of a carcinogen Company name: Joh... photo #1
313   Comments Comment

Recall notice

Innoveix Pharmaceuticals products - recalled due to lack of sterility assurance, USA

4 years ago •source fda.gov • details

Company name: Innoveix Pharmaceuticals, Inc.
Brand name: Innoveix Pharmaceuticals, Inc.
Product recalled: Injectable Semorelin / Ipamorelin 3mg and injectable AOD-9604 3mg
Reason of the recall: Potential lack of sterility assurance
FDA Recall date: July 13, 2021
Recall details: Innoveix Pharmaceuticals, Inc. is voluntarily recalling the following lots… See more

#recall #drugs #unitedstates

Recalls Innoveix Pharmaceuticals products - recalled due to lack of sterility assurance Company name: Innove... photo #1
312   Comments Comment

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