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Safety Reports: Drugs

Updated:

Real Time Reports

Recall notice

Imperial Dietary Supplement for Male Enhancement - recalled due to Undeclared Sildenafil & Tadalafil, USA

4 years ago •source fda.gov • details

Company name: S&B Shopper LLC
Brand name: Imperial
Product recalled: Dietary Supplement for Male Enhancement
Reason of the recall: Undeclared Sildenafil & Tadalafil
FDA Recall date: March 25, 2021
Recall details: S&B Shopper LLC is voluntarily recalling all lots of Imperial Extreme 2000mg capsules, to the consumer… See more

#blood #recall #drugs #unitedstates

312   Comments Comment

Recall notice

Acyclovir Sodium Injection- recalled due to Crystalization, USA

4 years ago •source fda.gov • details

Company name: Zydus Pharmaceuticals Inc.
Brand name: Zydus Pharmaceuticals
Product recalled: Acyclovir Sodium Injection, 50 mg/mL, 10 mL and 20 mL vials
Reason of the recall: Due to Crystalization
FDA Recall date: March 25, 2021
Recall details: Pennington, NJ, Zydus Pharmaceuticals (USA) Inc. is voluntarily recalling four… See more

#blood #recall #drugs #unitedstates

Recalls Acyclovir Sodium Injection- recalled due to Crystalization Company name: Zydus Pharmaceuticals Inc.... photo #1
313   Comments Comment

Recall notice

ChloraPrep 3 mL Applicator - recalled due to potential fungal contamination, USA

4 years ago •source fda.gov • details

Company name: (Becton, Dickinson and Company)
Brand name: ChloraPrep; BD ChloraPrep
Product recalled: ChloraPrep 3 mL Applicator
Reason of the recall: Potential Aspergillus penicillioides contamination
FDA Recall date: March 24, 2021
Recall details: BD (Becton, Dickinson and Company), a leading global medical technology company, has revised its… See more

#recall #drugs #unitedstates

312   Comments Comment

Recall notice

Durisan Antimicrobial Hand Sanitizer - recalled due to microbial contamination, USA

4 years ago •source fda.gov • details

Company name: Sanit Technologies LLC d/b/a Durisan
Brand name: Durisan
Product recalled: Antimicrobial Hand Sanitizer
Reason of the recall: Due to microbial contamination
FDA Recall date: March 24, 2021
Recall details: Sanit Technologies LLC d/b/a Durisan announces a voluntary recall of the lots listed in the table… See more

#recall #drugs #unitedstates

Recalls Durisan Antimicrobial Hand Sanitizer - recalled due to microbial contamination Company name: Sanit T... photo #1
313   Comments Comment

Recall notice

Telmisartan Tablets, USP, 20 mg - recalled due to Label Mix-Up, USA

4 years ago •source fda.gov • details

Company name: Alembic Pharmaceuticals, Inc.
Brand name: Alembic
Product recalled: Telmisartan Tablets, USP, 20 mg
Reason of the recall: Incorrect Product Strength on Label
FDA Recall date: March 24, 2021
Recall details: Bridgewater, NJ, Alembic Pharmaceuticals, Inc is voluntarily recalling one lot of Telmisartan Tablets, USP, 20… See more

#blood #recall #drugs #unitedstates

Recalls Telmisartan Tablets, USP, 20 mg - recalled due to Label Mix-Up Company name: Alembic Pharmaceuticals... photo #1
313   Comments Comment

Recall notice

Heal the World Hand Sanitizer - recalled due to risk of ingestion, United States

4 years ago •source fda.gov • details

Company name: PNHC, LLC d/b/a Heal the World
Brand name: Heal the World
Product recalled: Hand Sanitizer
Reason of the recall: Because they resemble water bottles; risk of ingestion
FDA Recall date: March 17, 2021
Recall details: Raleigh, North Carolina, PNHC, LLC, d/b/a Heal the World, is … See more

#recall #drugs #unitedstates

Recalls Heal the World Hand Sanitizer - recalled due to risk of ingestion Company name: PNHC, LLC d/b/a Hea... photo #1
312   Comments Comment

Recall notice

Sagent Phenylephrine Hydrochloride Injection - recalled due to lack of sterility, USA

4 years ago •source fda.gov • details

Company name: Sagent Pharmaceuticals, Inc.
Brand name: Sagent
Product recalled: Phenylephrine Hydrochloride Injection
Reason of the recall: Lack of sterility assurance
FDA Recall date: March 11, 2021
Recall details: Sagent Pharmaceuticals, Inc. today announced the voluntary nationwide recall of three lots of Phenylephrine Hydrochloride Injection, USP (10… See more

#blood #recall #drugs #unitedstates

Recalls Sagent Phenylephrine Hydrochloride Injection - recalled due to lack of sterility Company name: Sagen... photo #1
312   Comments Comment

Recall notice

Spironolactone TB 25MG, 50MG - recalled due to incorrect strength, USA

4 years ago •source fda.gov • details

Company name: Bryant Ranch Prepack
Brand name: BRP Pharmaceuticals
Product recalled: Spironolactone TB 25MG and 50MG
Reason of the recall: Incorrect strength displayed on the label
FDA Recall date: March 09, 2021
Recall details: Company Announcement Bryant Ranch Prepack is voluntarily recalling 4 lots of Spironolactone tablets… See more

#blood #recall #drugs #unitedstates

Recalls Spironolactone TB 25MG, 50MG - recalled due to incorrect strength Company name: Bryant Ranch Prepack... photo #1
313   Comments Comment

Recall notice

Enoxaparin Sodium Injection, USP - recalled due incorrect dosage listed, USA

4 years ago •source fda.gov • details

Company name: Apotex Corp
Brand name: Apotex Corp.
Product recalled: Enoxaparin Sodium Injection, USP
Reason of the recall: Packaging error resulting in incorrect dosage listed
FDA Recall date: February 03, 2021
Recall details: Apotex Corp is voluntarily recalling two (2) batches of Enoxaparin Sodium Injection, USP to… See more

#blood #drugs #unitedstates

Recalls Enoxaparin Sodium Injection, USP - recalled due incorrect dosage listed Company name: Apotex Corp B... photo #1
312   Comments Comment

Recall notice

Meitheal Cisatracurium Besylate Injection - recalled due to Mislabeling, USA

4 years ago •source fda.gov • details

Company name: Meitheal Pharmaceuticals, Inc.
Brand name: Meitheal Pharmaceuticals, Inc.
Product recalled: Cisatracurium Besylate Injection, USP 10mg per 5mL
Reason of the recall: Mislabeling
FDA Recall date: January 27, 2021
Recall details: Meitheal Pharmaceuticals, Inc. (“Meitheal”), announced today that it is voluntarily recalling one (1) lot of… See more

#blood #recall #drugs #unitedstates

Recalls Meitheal Cisatracurium Besylate Injection - recalled due to Mislabeling Company name: Meitheal Pha... photo #1
312   Comments Comment

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