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Safety Reports: Drugs

Updated:

Real Time Reports

Recall notice

WishGarden Herbal Remedies Happy Ducts Compress - recalled as it may be contaminated with Cronobacter sakazakii., USA

5 years ago •source fda.gov • details

Company name: WishGarden Herbs
Brand name: WishGarden Herbal Remedies
Product recalled: Happy Ducts Compress
Reason of the recall: Product may be contaminated with Cronobacter sakazakii.
FDA Recall date: December 01, 2020
Recall details: WishGarden Herbs, Inc. is voluntarily recalling one lot of Happy Ducts Compress to the… See more

#recall #drugs #unitedstates

Recalls WishGarden Herbal Remedies Happy Ducts Compress - recalled as it may be contaminated with Cronobacte... photo #1
312   Comments Comment

Recall notice

Fresenius Kabi USA Dexmedetomidine HCL in 0.9% Sodium Chloride Injection - recalled due to cross contamination with Lidocaine, USA

5 years ago •source fda.gov • details

Company name: Fresenius Kabi USA
Brand name: Fresenius Kabi USA
Product recalled: Dexmedetomidine HCL in 0.9% Sodium Chloride Injection
Reason of the recall: Cross Contamination with Lidocaine
FDA Recall date: November 19, 2020
Recall details: Fresenius Kabi USA is voluntarily recalling a single lot of Dexmedetomidine HCl… See more

#crosscontamination #recall #drugs #unitedstates

Recalls Fresenius Kabi USA Dexmedetomidine HCL in 0.9% Sodium Chloride Injection - recalled due to cross con... photo #1
312   Comments Comment

Recall notice

Lohxa Chlorhexidine Gluconate Oral Rinse USP, 0.12% Alcohol free - recalled as it may be contaminated with Burkholderia lata, USA

5 years ago •source fda.gov • details

Company name: Lohxa, LLC
Brand name: Lohxa
Product recalled: Chlorhexidine Gluconate Oral Rinse USP, 0.12% Alcohol free
Reason of the recall: May be contaminated with Burkholderia lata
FDA Recall date: November 09, 2020
Recall details: Lohxa, LLC is voluntarily recalling Chlorhexidine Gluconate Oral Rinse USP, 0.12% Alcohol… See more

#recall #drugs #unitedstates

Recalls Lohxa Chlorhexidine Gluconate Oral Rinse USP, 0.12% Alcohol free - recalled as it may be contaminate... photo #1
312   Comments Comment

Recall notice

Nostrum Laboratories Metformin HCl Extended Release Tablets, USP 500 mg - recalled due to NDMA exceeds acceptable daily intake limit, USA

5 years ago •source fda.gov • details

Company name: Nostrum Laboratories
Brand name: Nostrum Laboratories
Product recalled: Metformin HCl Extended Release Tablets, USP 500 mg
Reason of the recall: NDMA exceeds acceptable daily intake limit
FDA Recall date: November 03, 2020
Recall details: Nostrum Laboratories, Inc. is voluntarily recalling 2 (two) lots of Metformin… See more

#blood #recall #drugs #unitedstates

312   Comments Comment

Recall notice

Nostrum Laboratories Metformin HCl Extended Release Tablets, USP 750 mg - recalled due to NDMA exceeds acceptable daily intake limit, USA

5 years ago •source fda.gov • details

Company name: Nostrum Laboratories
Brand name: Nostrum Laboratories
Product recalled: Metformin HCl Extended Release Tablets, USP 750 mg
Reason of the recall: NDMA exceeds acceptable daily intake limit
FDA Recall date: November 02, 2020
Recall details: Kansas City, Missouri, Nostrum Laboratories, Inc. is voluntarily recalling 2 (two)… See more

#drugs #blood #recall #unitedstates

312   Comments Comment

Recall notice

Paroex Chlorhexidine Gluconate Oral Rinse, 4 oz and 16 oz - recalled due to potential contamination with Burkholderia lata, USA

5 years ago •source fda.gov • details

Company name: Sunstar Americas, Inc.
Brand name: Paroex
Product recalled: Paroex Chlorhexidine Gluconate Oral Rinse, 4 oz and 16 oz
Reason of the recall: Potential contamination with Burkholderia lata
FDA Recall date: October 28, 2020
Recall details: Sunstar Americas, Inc. (SAI) is voluntarily recalling Paroex® Chlorhexidine Gluconate… See more

#drugs #unitedstates #wrap

Recalls Paroex Chlorhexidine Gluconate Oral Rinse, 4 oz and 16 oz - recalled due to potential contamination... photo #1
312   Comments Comment

Recall notice

Time-Cap Labs Inc. Metformin Hydrochloride for Extended-Release Tablets, USP 500 mg and 700 mg - recalled due to the Detection of N-Nitrosodimethylamine (NDMA) Impurity, USA

5 years ago •source fda.gov • details

Company name: Marksans Pharma Limited
Brand name: Time-Cap Labs Inc.
Product recalled: Metformin Hydrochloride for Extended-Release Tablets, USP 500 mg and 700 mg
Reason of the recall: Due to the Detection of N-Nitrosodimethylamine (NDMA) Impurity
FDA Recall date: October 05, 2020
Recall details: Marksans Pharma Limited, India… See more

#blood #recall #drugs #unitedstates

Recalls Time-Cap Labs Inc. Metformin Hydrochloride for Extended-Release Tablets, USP 500 mg and 700 mg - rec... photo #1
312   Comments Comment

Recall notice

Smart Care Hand sanitizer packaged in 0.84 oz. pouches - recalled due to product is packaged in containers resembling a food and drink pouch, United States

5 years ago •source fda.gov • details

Company name: Ashtel Studios
Brand name: Smart Care
Product recalled: Hand sanitizer packaged in 0.84 oz. pouches
Reason of the recall: Product is packaged in containers resembling a food and drink pouch
FDA Recall date: October 02, 2020
Recall details: Company Announcement Ashtel Studios has announced a… See more

#handsanitizer #drugs #unitedstates

Recalls Smart Care Hand sanitizer packaged in 0.84 oz. pouches - recalled due to product is packaged in cont... photo #1
312   Comments Comment

Recall notice

Riomet ER - recalled due to due to NDMA Impurity, USA

5 years ago •source fda.gov • details

Company name: Sun Pharmaceutical Industries
Brand name: Riomet ER
Product recalled: Metformin Hydrochloride for Extended-Release Oral Suspension
Reason of the recall: Due to the Detection of N-Nitrosodimethylamine (NDMA) Impurity
FDA Recall date: September 23, 2020
Recall details: Sun Pharmaceutical Industries, Inc. (SUN PHARMA), a wholly owned subsidiary… See more

#recall #drugs #unitedstates

Recalls Riomet ER - recalled due to due to NDMA Impurity Company name: Sun Pharmaceutical Industries Brand... photo #1
312   Comments Comment

Recall notice

Acella Pharmaceuticals, LLC Thyroid Tablets - recalled due to Sub Potency, USA

5 years ago •source fda.gov • details

Company name: Acella Pharmaceuticals, LLC
Brand name: NP Thyroid 15 & NP Thyroid120
Product recalled: Thyroid Tablets
Reason of the recall: Sub Potency
FDA Recall date: September 17, 2020
Recall details: Acella Pharmaceuticals, LLC is voluntarily recalling one lot of 15-mg and one lot of 120-mg NP… See more

#drugs #unitedstates #sub

Recalls Acella Pharmaceuticals, LLC Thyroid Tablets - recalled due to Sub Potency Company name: Acella Pharm... photo #1
312   Comments Comment

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