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Safety Reports: Drugs

Updated:

Real Time Reports

Recall notice

Nostrum Laboratories, Inc. Metformin HCl Extended Release Tablets, USP 750 mg - recalled due to Due to levels of nitrosamine impurities above the ADI limit of 96 ng/day, USA

4 years ago •source fda.gov • details

Company name: Nostrum Laboratories, Inc.
Brand name: Nostrum Laboratories, Inc.
Product recalled: Metformin HCl Extended Release Tablets, USP 750 mg
Reason of the recall: Due to levels of nitrosamine impurities above the ADI limit of 96 ng/day
FDA Recall date: January 25, 2021
Recall details: Kansas City,… See more

#blood #drugs #unitedstates

Recalls Nostrum Laboratories, Inc. Metformin HCl Extended Release Tablets, USP 750 mg - recalled due to Due... photo #1
312   Comments Comment

Recall notice

Fresenius Kabi USA Ketorolac Tromethamine Injection, USP, 30 mg/mL - recalled due to Presence of particulate matter, USA

5 years ago •source fda.gov • details

Company name: Fresenius Kabi USA
Brand name: Fresenius Kabi
Product recalled: Ketorolac Tromethamine Injection, USP, 30 mg/mL
Reason of the recall: Presence of particulate matter
FDA Recall date: January 08, 2021
Recall details: Fresenius Kabi USA is voluntarily recalling a single lot of Ketorolac Tromethamine Injection, USP,… See more

#blood #recall #drugs #unitedstates

Recalls Fresenius Kabi USA Ketorolac Tromethamine Injection, USP, 30 mg/mL - recalled due to Presence of par... photo #1
315   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: January 04, 2021
Recall details: Company Announcement Nostrum Laboratories, Inc. is voluntarily recalling one lot of… See more

#blood #drugs #unitedstates

312   Comments Comment

Recall notice

Soho Fresh 70% Rubbing Alcohol - recalled due to Contaminated with Methanol, USA

5 years ago •source fda.gov • details

Company name: Essaar Inc.
Brand name: Soho Fresh
Product recalled: 70% Rubbing Alcohol
Reason of the recall: Contaminated with Methanol
FDA Recall date: January 04, 2021
Recall details: Company Announcement Essaar Inc. is voluntarily recalling lot 200528303 of Soho Fresh 70% Rubbing Alcohol in 33.81 oz. clear… See more

#handsanitizer #drugs #unitedstates

Recalls Soho Fresh 70% Rubbing Alcohol - recalled due to Contaminated with Methanol Company name: Essaar... photo #1
314   Comments Comment

Recall notice

GUM Paroex Chlorhexidine Gluconate Oral Rinse - recalled due to potential contamination with Burkholderia lata, USA

5 years ago •source fda.gov • details

Company name: Precision Dose Inc.
Brand name: GUM Paroex
Product recalled: Paroex Chlorhexidine Gluconate Oral Rinse, 15 mL unit dose cups
Reason of the recall: Potential contamination with Burkholderia lata
FDA Recall date: December 31, 2020
Recall details: Company Announcement Precision Dose, Inc. is voluntarily recalling all… See more

#drugs #unitedstates

Recalls GUM Paroex Chlorhexidine Gluconate Oral Rinse - recalled due to potential contamination with Burkhol... photo #1
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: December 28, 2020
Recall details: Schaumburg, Illinois, Sunstar Americas, Inc. (SAI) is voluntarily recalling Paroex®… See more

#recall #drugs #unitedstates #wrap

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

Recall notice

IMC Wash-Free Hand Sanitizer - recalled due to Undeclared Methanol, USA

5 years ago •source fda.gov • details

Company name: Shane Erickson, Inc. DBA Innovative Marketing Consultants
Brand name: IMC
Product recalled: Wash-Free Hand Sanitizer
Reason of the recall: Undeclared Methanol
FDA Recall date: December 23, 2020
Recall details: Shane Erickson, Inc. is voluntarily recalling lot 2020/05/11 and MFG: 2020/05/10 L/N: 20200510-3 of imc Wash-Free… See more

#drugs #unitedstates

Recalls IMC Wash-Free Hand Sanitizer - recalled due to Undeclared Methanol Company name: Shane Erickson, In... photo #1
312   Comments Comment

Recall notice

Torrent Pharmaceuticals Limited Anagrelide Capsule USP 1mg - recalled due to dissolution test failure, USA

5 years ago •source fda.gov • details

Company name: Torrent Pharmaceuticals Limited
Brand name: Torrent Pharmaceuticals Limited
Product recalled: Anagrelide Capsule USP 1mg
Reason of the recall: Due to dissolution test failure
FDA Recall date: December 09, 2020
Recall details: Torrent Pharmaceuticals Limited is voluntarily recalling one lot of Anagrelide Capsules, USP to the… See more

#blood #recall #drugs #unitedstates #sub

Recalls Torrent Pharmaceuticals Limited Anagrelide Capsule USP 1mg - recalled due to dissolution test failu... photo #1
312   Comments Comment

Recall notice

WishGarden Herbs Remedies Cord Care and Goldenseal Powder - recalled due to potential Cronobacter sakazakii contamination, USA

5 years ago •source fda.gov • details

Company name: WishGarden Herbs, Inc.
Brand name: WishGarden Herbal Remedies
Product recalled: Cord Care and Goldenseal Powder
Reason of the recall: Product may be contaminated with Cronobacter sakazakii
FDA Recall date: December 04, 2020
Recall details: Company Announcement WishGarden Herbs, Inc. is voluntarily recalling, to the consumer… See more

#drugs #unitedstates

Recalls WishGarden Herbs Remedies Cord Care and Goldenseal Powder - recalled due to potential Cronobacter sa... photo #1
312   Comments Comment

Recall notice

Regenecare HA Topical Anesthetic Hydrogel - recalled due to Burkholderia cepecia contamination.

5 years ago •source fda.gov • details

Company name: MPM Medical, LLC
Brand name: MPM Medical
Product recalled: Regenecare HA Topical Anesthetic Hydrogel
Reason of the recall: Burkholderia cepecia contamination.
FDA Recall date: December 02, 2020
Recall details: MPM Medical is voluntarily recalling one lot of Regenecare HA Hydrogel to the consumer level. Following… See more

#blood #drugs #unitedstates

Recalls Regenecare HA Topical Anesthetic Hydrogel - recalled due to Burkholderia cepecia contamination. Comp... photo #1
312   Comments Comment

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