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Safety Reports: Recall

Updated: March 31, 2021 8:00 PM

Real Time Reports

Recall notice

Guanfacine Extended-Release Tablets 2mg - recalled due to Quetiapine Fumarate, USA

4 years ago •source fda.gov • details

Company name: Apotex Corp.
Brand name: Apotex Corp.
Product recalled: Guanfacine Extended-Release Tablets 2mg
Reason of the recall: Trace amounts of Quetiapine Fumarate
FDA Recall date: March 31, 2021
Recall details: Weston, Florida, Apotex Corp is voluntarily recalling three (3) lots of Guanfacine Extended-Release Tablets 2mg to… See more

#blood #recall #drugs #unitedstates

Recalls Guanfacine Extended-Release Tablets 2mg - recalled due to Quetiapine Fumarate Company name: Apotex C... photo #1

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Recall notice

Thumbs Up 7, Shogun-X, 69MODE Supplements - recalled due to undeclared Sildenafil, Tadalafil, Vardenafil, USA

4 years ago •source fda.gov • details

Company name: Nuri Trading LLC
Brand name: Thumbs Up 7, Shogun-X, 69MODE
Product recalled: Dietary Supplement for male sexual enhancement
Reason of the recall: Undeclared Sildenafil, Tadalafil, Vardenafil
FDA Recall date: March 31, 2021
Recall details: Nuri Trading is voluntarily recalling all lots within expiry of Shogun-X… See more

#blood #recall #drugs #unitedstates

Recalls Thumbs Up 7, Shogun-X, 69MODE Supplements - recalled due to undeclared Sildenafil, Tadalafil, Varden... photo #1

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Recall notice

Thumbs Up 7 Blue 69K Male Supplement - recalled due to undeclared Sildenafil and Tadalafil, USA

4 years ago •source fda.gov • details

Company name: Bit & Bet LLC
Brand name: Thumbs Up 7
Product recalled: Blue 69K Dietary Supplement for male sexual enhancement
Reason of the recall: Undeclared Sildenafil and Tadalafil
FDA Recall date: March 30, 2021
Recall details: Bit & Bet LLC is voluntarily recalling all lots of… See more

#blood #recall #drugs #unitedstates

Recalls Thumbs Up 7 Blue 69K Male Supplement - recalled due to undeclared Sildenafil and Tadalafil Company n... photo #1

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Recall notice

Thumbs Up 7 Male Sexual Supplement - recalled due to undeclared Sildenafil and Tadalafil, USA

4 years ago •source fda.gov • details

Company name: Antoto-K
Brand name: Thumbs Up 7
Product recalled: Dietary Supplement for male sexual enhancement
Reason of the recall: Undeclared Sildenafil and Tadalafil
FDA Recall date: March 29, 2021
Recall details: Manassas, VA, Antoto-K is voluntarily recalling all lots of Thumbs Up 7 Red 70K, 10… See more

#blood #recall #drugs #unitedstates

Recalls Thumbs Up 7 Male Sexual Supplement - recalled due to undeclared Sildenafil and Tadalafil Company nam... photo #1

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Recall notice

Multiple Midwestern Dog and Cat Food brands - recalled due to Potential Salmonella, USA

4 years ago •source fda.gov • details

Company name: Midwestern Pet Foods
Brand name: Multiple brands
Product recalled: Dog and Cat Food
Reason of the recall: Potential Salmonella Contamination
FDA Recall date: March 27, 2021
Recall details: Midwestern Pet Foods, Evansville, Indiana is issuing a voluntary recall of specific expiration dates of certain dog… See more

#catfood #recall #dogfood #petfood #unitedstates

Recalls Multiple Midwestern Dog and Cat Food brands - recalled due to Potential Salmonella Company name: Mid... photo #1

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Recall notice

PremierZen male sexual enhancement - recalled due to Undeclared Sildenafil and Tadalafil, USA

4 years ago •source fda.gov • details

Company name: Namoo Enterprise LLC
Brand name: PremierZen
Product recalled: Dietary Supplement for male sexual enhancement
Reason of the recall: Undeclared Sildenafil and Tadalafil
FDA Recall date: March 26, 2021
Recall details: Little Ferry, NJ, Namoo Enterprise LLC is voluntarily recalling all lots within expiry of PremierZen… See more

#blood #recall #drugs #unitedstates

Recalls PremierZen male sexual enhancement - recalled due to Undeclared Sildenafil and Tadalafil Company nam... photo #1

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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

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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

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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

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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