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Safety Reports: Recall

Updated:

Real Time Reports

Recall notice

Major Dronabinol and Ziprasidone Hydrochloride capsules- recalled due to labeling mix-up, USA

2 years ago •source fda.gov • details

The Harvard Drug Group, LLC d/b/a Major Pharmaceutical and Rugby Laboratories is initiating a voluntary recall of a single lot of Dronabinol Capsules, USP, 2.5 mg and Ziprasidone Hydrochloride Capsules, 20 mg to the consumer level. The Harvard Drug Group, LLC received a customer complaint from a… See more

#recall #drugs #unitedstates

Recalls Major Dronabinol and Ziprasidone Hydrochloride capsules- recalled due to labeling mix-up The Harvard... photo #1
312   Comments Comment

Recall notice

Bacaolinita - recalled due to Unapproved PEG-40 Hydrogenated Castor Oil, USA

2 years ago •source fda.gov • details

PROCAPS S.A. DE C.V. from San Salvador, El Salvador is voluntarily recalling Laboratorios Lopez's Bacaolinita 8 FL OZ, a dietary supplement, due to the label of the product not declaring, PEG-40 hydrogenated castor oil as an inactive ingredient on the labeling. Safety data on the oral ingestion… See more

#vitamins #recall #unitedstates

Recalls Bacaolinita - recalled due to Unapproved PEG-40 Hydrogenated Castor Oil PROCAPS S.A. DE C.V. from Sa... photo #1
312   Comments Comment

Recall notice

G-SUPRESS DX pediatric drops- recalled due to Incorrect Packaging, Puerto Rico

2 years ago •source fda.gov • details

Novis PR LLC is voluntarily recalling Lot D20911 Exp 10/25 of G-Supress DX Pediatric Drops to the consumer level. Some cartons of the product have been found to contain incorrect product inside. Incorrect product inside is an anesthetic/analgesic and not a brand of Novis PR LLC. Lot… See more

#drugs #recall #puertorico

Recalls G-SUPRESS DX pediatric drops- recalled due to Incorrect Packaging Novis PR LLC is voluntarily recall... photo #1
48   Comments Comment

Recall notice

Walnut Wearable Smart Thermometer - recalled due to Potential for injuries, USA

2 years ago •source fda.gov • details

BearCare, Inc. is initiating a voluntary recall of its rechargeable Walnut Wearable Smart Thermometer (Walnut Thermometer) due to reports of injuries, including skin burns, by users. The Walnut Thermometer is an over-the-counter rechargeable device intended for continuous chest temperature monitoring of children ages 0-6 years which can… See more

#amazon #walmart #recall #medicaldevices #unitedstates

Recalls Walnut Wearable Smart Thermometer - recalled due to Potential for injuries BearCare, Inc. is initiat... photo #1
312   Comments Comment

Recall notice

Lily’s Kitchen products - recalled due to extraneous materials, UK

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

Lily’s Kitchen is recalling a batch of its Fishy Fish Pie and a batch of Chicken and Turkey Casserole because they may contain pieces of plastic. The possible presence of plastic makes the products unsafe to eat for your pets and presents a potential choking hazard. These… See more

#recall #petfood #unitedkingdom

Recalls Lily’s Kitchen products - recalled due to extraneous materials Lily’s Kitchen is recalling a batch o... photo #1
159   Comments Comment

Recall notice

Pilot COVID-19 At-Home Test - recalled due to Due to microbial contamination, USA

2 years ago •source fda.gov • details

SD Biosensor, Inc. is requesting that consumers stop using and dispose of specific Pilot COVID-19 At-Home Tests in the United States because potentially harmful bacteria were found in the tube with liquid inside (pouch 2 of the kits). The affected test kits were distributed by Roche Diagnostics… See more

#recall #medicaldevices #unitedstates

Recalls Pilot COVID-19 At-Home Test - recalled due to Due to microbial contamination SD Biosensor, Inc. is r... photo #1
312   Comments Comment

Recall notice

Akorn human & animal drug products update - recalled due to discontinuation of the Quality program, USA

2 years ago •source fda.gov • details

The Akorn Trustee is initiating a voluntary recall of various within-expiry human and animal products as a result of the closures and discontinuation of the Quality activities of these marketed products. The discontinuation of the Quality program means the company will not be able to support or… See more

#recall #drugs #unitedstates

Recalls Akorn human & animal drug products update - recalled due to discontinuation of the Quality program T... photo #1
312   Comments Comment

Recall notice

Advil sold by Family Dollar – Recalled due to stored outside of label temperature, USA

2 years ago •source fda.gov • details

Family Dollar is initiating a voluntary retail level product recall of certain over-the-counter drug products regulated by the U.S. Food and Drug Administration (FDA) that were stored and shipped to certain stores on or around June 1, 2022 through March 31, 2023 due to product being stored… See more

#recall #familydollar #unitedstates

Recalls Advil sold by Family Dollar – Recalled due to stored outside of label temperature Family Dollar is i... photo #1
312   Comments Comment

Recall notice

Del Maguey Copitas-Artisan ceramicware cups - recalled due to exceed levels for leachable lead, USA

2 years ago •source fda.gov • details

Del Maguey Co., New York, NY is conducting a voluntary recall of certain ceramicware cups called copitas – small artisan cups traditionally used for drinking mezcal – because they may exceed FDA guidance levels for leachable lead. The copitas were distributed free-of-charge to consumers at retail locations,… See more

#recall #drugs #unitedstates

Recalls Del Maguey Copitas-Artisan ceramicware cups - recalled due to exceed levels for leachable lead Del M... photo #1
312   Comments Comment

Recall notice

Mayne Pharma Inc. FENTANYL Buccal Tablets CII - recalled due to Safety updates omissions, USA

2 years ago •source fda.gov • details

Teva Pharmaceuticals USA, has initiated a voluntary nationwide recall of specific lots of various strengths of FENTANYL Buccal Tablets CII to the Consumer Level. Teva USA manufactured and labeled these product lots exclusively for Mayne Pharma Inc. under Mayne's label. This recall has been initiated because safety… See more

#recall #drugs #unitedstates

Recalls Mayne Pharma Inc. FENTANYL Buccal Tablets CII - recalled due to Safety updates omissions Teva Pharma... photo #1
312   Comments Comment

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