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Safety Reports: Recall

Updated:

Real Time Reports

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

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

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 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

Happy Hounds Wales Ltd raw dog food products - recalled because of potential Salmonella contamination, UK

5 years ago •source food.gov.uk • details

The FSA announced the recall of raw dog food products by Happy Hounds Wales Ltd because they may contain salmonella.

FSA advises consumers not to use the recalled product. Instead, return it to the store from where it was bought for a full refund. When handling and… See more

#recall #dogfood #petfood #unitedkingdom #beef #chicken

Recalls Happy Hounds Wales Ltd raw dog food products - recalled because of potential Salmonella contaminatio... photo #1
79   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

#recall #crosscontamination #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

#blood #recall #drugs #unitedstates

312   Comments Comment

Recall notice

Eishindo Jelly Cups - recalled due to product poses a choking hazard., USA

5 years ago •source fda.gov • details

Company name: Hadson Toko Trading Co., Inc.
Brand name: Eishindo
Product recalled: Jelly Cups
Reason of the recall: Product poses a choking hazard.
FDA Recall date: October 14, 2020
Recall details: HADSON (TOKO) TRADING CO., INC. OF MASPETH, NY is recalling its 28.2oz (800g) bags of EISHINDO… See more

#recall #foodsafetyissue #unitedstates

Recalls Eishindo Jelly Cups - recalled due to product poses a choking hazard. Company name: Hadson Toko Trad... photo #1
312   Comments Comment

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