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Safety Reports: Recall

Updated: May 17, 2021 4:00 PM

Real Time Reports

Recall notice

Durisan Hand sanitizer - recalled due to Burkholderia contaminans contamination, USA

4 years ago •source fda.gov • details

Company name: Sanit Technologies LLC d/b/a Durisan
Brand name: Durisan
Product recalled: Hand sanitizer
Reason of the recall: Product is contaminated with Burkholderia contaminants
FDA Recall date: May 17, 2021
Recall details: Sanit Technologies LLC d/b/a Durisan is updating its previously announced voluntary recall of Durisan Non-Alcohol… See more

#recall #drugs #unitedstates

Recalls Durisan Hand sanitizer - recalled due to Burkholderia contaminans contamination Company name: Sanit... photo #1

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Recall notice

Goose Creek, COCO TKO Hand Sanitizer - recalled due to presence of Methanol, USA

4 years ago •source fda.gov • details

Company name: Scentsational Soaps & Candles, Inc.
Brand name: Goose Creek, COCO TKO
Product recalled: Hand Sanitizer
Reason of the recall: Presence of Methanol (Wood Alcohol), Benzene and Acetaldehyde
FDA Recall date: May 13, 2021
Recall details: Scentsational Soaps & Candles, Inc., has voluntarily expanded its April… See more

#blood #recall #drugs #unitedstates #lemonade #soda

Recalls Goose Creek, COCO TKO Hand Sanitizer - recalled due to presence of Methanol Company name: Scentsatio... photo #1

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Recall notice

Medically Minded Hand Sanitizer - recalled due to presence of methanol, USA

4 years ago •source fda.gov • details

Company name: Global Sanitizers
Brand name: Medically Minded
Product recalled: Hand Sanitizer
Reason of the recall: Presence of methanol
FDA Recall date: May 13, 2021
Recall details: Las Vegas, NV, Global Sanitizers is voluntarily recalling 50 thousand units of Medically Minded hand sanitizers, lot numbers: E212020 &… See more

#recall #drugs #unitedstates

Recalls Medically Minded Hand Sanitizer - recalled due to presence of methanol Company name: Global Sanitize... photo #1

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Recall notice

Dibar Nutricional S. de R.L. de C.V. Hand Sanitizer - recalled due to Presence of methanol, USA

4 years ago •source fda.gov • details

Company name: Dibar Nutricional S. de R.L. de C.V.
Brand name: DIBAR Labs, ProtectoRx
Product recalled: Hand Sanitizer
Reason of the recall: Presence of methanol
FDA Recall date: May 12, 2021
Recall details: Company Announcement Morelia, Michoacán, Mexico, Dibar Nutricional S. de R.L. De C.V. (“Dibar”) is… See more

#recall #drugs #unitedstates

Recalls Dibar Nutricional S. de R.L. de C.V. Hand Sanitizer - recalled due to Presence of methanol Company n... photo #1

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Recall notice

Imperia Elita Vitaccino Coffee dietary supplement - recalled due to undeclared Sibutramine and Fluoxetine, USA

4 years ago •source fda.gov • details

Company name: Dash Xclusive
Brand name: Imperia Elita
Product recalled: Vitaccino Coffee weight loss and anxiety dietary supplement
Reason of the recall: Undeclared Sibutramine and Fluoxetine
FDA Recall date: May 11, 2021
Recall details: Glendale, California, Dash Xclusive is voluntarily recalling all lots of Imperia Elita Vitaccino… See more

#vitamins #blood #recall #unitedstates #coffee

Recalls Imperia Elita Vitaccino Coffee dietary supplement - recalled due to undeclared Sibutramine and Fluox... photo #1

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Recall notice

Poseidon Supplements for sexual enhancement - recalled due to undeclared Tadalafil, USA

4 years ago •source fda.gov • details

Company name: Yamtun7
Brand name: Poseidon
Product recalled: Male Sexual Enhancement Dietary Supplement
Reason of the recall: Undeclared Tadalafil and Sildenafil
FDA Recall date: May 11, 2021
Recall details: Delray Beach, Florida, Yamtun7 is voluntarily recalling all lots of Poseidon Platinum 3500 to the consumer level. FDA… See more

#recall #blood #drugs #unitedstates

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Recall notice

Novo Nordisk Product Samples - recalled due to improper storage temperature, USA

4 years ago •source fda.gov • details

Company name: Novo Nordisk
Brand name: Levemir, Tresiba, Fiasp, Novolog and Xultophy
Product recalled: Product Samples
Reason of the recall: Due to improper storage temperature conditions
FDA Recall date: May 10, 2021
Recall details: Novo Nordisk is voluntarily recalling 1,468 product samples listed in the table below… See more

#blood #recall #drugs #unitedstates

Recalls Novo Nordisk Product Samples - recalled due to improper storage temperature Company name: Novo Nordi... photo #1

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Recall notice

Hospira 0.5% Bupivacaine Hydrochloride Injection and 1% Lidocaine HCl Injection - recalled due to mislabeling, USA

4 years ago •source fda.gov • details

Company name: Hospira, Inc.
Brand name: Hospira, Inc.
Product recalled: 0.5% Bupivacaine Hydrochloride Injection, USP 30 mL and 1% Lidocaine HCl Injection, USP 30 mL
Reason of the recall: Due to mislabeling
FDA Recall date: May 04, 2021
Recall details: Hospira, Inc., a Pfizer company, is voluntarily… See more

#rats #recall #drugs #unitedstates

Recalls Hospira 0.5% Bupivacaine Hydrochloride Injection and 1% Lidocaine HCl Injection - recalled due to mi... photo #1

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Recall notice

Hospira Sterile Water Single Dose Glass - recalled due to visible particulate, USA

4 years ago •source fda.gov • details

Company name: Hospira, Inc.
Brand name: Hospira, Inc.
Product recalled: Sterile Water for Injection, USP, 100 mL Single Dose Glass Fliptop Vial
Reason of the recall: Due to visible particulate
FDA Recall date: May 04, 2021
Recall details: Hospira, Inc., a Pfizer company, is voluntarily recalling lot… See more

#recall #drugs #unitedstates

Recalls Hospira Sterile Water Single Dose Glass - recalled due to visible particulate Company name: Hospira,... photo #1

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Recall notice

Acella NP Thyroid (Thyroid Tablets, USP) - recalled due to sub potency, USA

4 years ago •source fda.gov • details

Company name: Acella Pharmaceuticals, LLC
Brand name: Acella
Product recalled: NP Thyroid (Thyroid Tablets, USP)
Reason of the recall: Sub potency
FDA Recall date: April 30, 2021
Recall details: Acella Pharmaceuticals, LLC, is voluntarily recalling certain lots listed in the Tables 1 and 2 below of 15-mg,… See more

#recall #drugs #unitedstates #sub