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Safety Reports: Recall

Updated:

Real Time Reports

Recall notice

Family Dollar Over-the-Counter Drug & Medical Device products - recalled due to improper storage temperature, USA

2 years ago •source fda.gov • details

Family Dollar is initiating a voluntary retail-level product recall of certain over-the-counter drugs and medical devices regulated by the U.S. Food and Drug Administration (FDA). These items were stored outside of labeled temperature requirements by Family Dollar and inadvertently shipped to certain stores on or around June… See more

#medicaldevices #drugs #recall #familydollar #unitedstates

Recalls Family Dollar Over-the-Counter Drug & Medical Device products - recalled due to improper storage tem... photo #1
312   Comments Comment

Recall notice

KVK-Tech Betaxolol Tablets, USP - recalled due to Potential Presence of Oxycodone HCl tablet, USA

2 years ago •source fda.gov • details

KVK-Tech, Inc. is voluntarily recalling one lot (Batch Number: 17853A; "the batch") of Betaxolol Tablets, USP 10 mg, White, Round, film coated biconvex tablets, debossed "K" above bisect "13" on one side and plain on the other side" to the consumer level. The batch was distributed nationwide… See more

#recall #drugs #unitedstates

Recalls KVK-Tech Betaxolol Tablets, USP - recalled due to Potential Presence of Oxycodone HCl tablet KVK-Te... photo #1
312   Comments Comment

Recall notice

Hospira Sodium Bicarbonate & Lidocaine HCl Injections - recalled due to potential presence of glass particulate matter, USA

2 years ago •source fda.gov • details

Hospira, Inc., a Pfizer company, is voluntarily recalling 4.2% Sodium Bicarbonate Injection, USP, 5 mEq/10mL vial; 1% Lidocaine HCl Injection, USP, 50 mg/5mL vial; and 2% Lidocaine HCl Injection, USP, 100 mg/5mL vial to the user level due to the potential presence of glass particulate matter. To… See more

#blood #recall #drugs #unitedstates

Recalls Hospira Sodium Bicarbonate & Lidocaine HCl Injections - recalled due to potential presence of glass... photo #1
312   Comments Comment

Recall notice

Ion & Restore brands Nasal Sprays - recalled due to due to Microbial Contamination, USA

2 years ago •source fda.gov • details

Biomic Sciences is voluntarily recalling all lots of ION* Sinus Support, ION* Biome Sinus, and Restore Sinus Spray products to the consumer level. FDA testing found the product to contain microbial contamination identified as Microbacterium sp., Fictibacillus sp., Bacillus sp., (primarily B. malikii), and Paenibacillus sp (these… See more

#recall #drugs #unitedstates

Recalls Ion & Restore brands Nasal Sprays - recalled due to due to Microbial Contamination Biomic Sciences i... photo #1
312   Comments Comment

Recall notice

Merck Animal Health Banamine/Banamine-S Update - recalled due to presence of particulate matter, USA

2 years ago •source fda.gov • details

Merck Animal Health, known as MSD Animal Health outside of the United States and Canada, a division of Merck & Co., Inc., Rahway, N.J., USA (NYSE:MRK), is voluntarily recalling 4 additional batches of BANAMINE® / BANAMINE®-S (flunixin meglumine injection) 50 mg/mL in the United States, used for… See more

#recall #drugs #unitedstates

Recalls Merck Animal Health Banamine/Banamine-S Update - recalled due to presence of particulate matter Merc... photo #1
312   Comments Comment

Recall notice

BREXAFEMME® Antifungal oral medication - recalled due to Potential cross contamination, USA

2 years ago •source fda.gov • details

SCYNEXIS, Inc. is conducting a voluntary nationwide recall of 2 lots of BREXAFEMME® (ibrexafungerp tablets) to the consumer level in the US market due to potential cross contamination with a non- antibacterial ß-lactam drug substance in the ibrexafungerp citrate used to manufacture the BREXAFEMME® tablets. During a… See more

#recall #drugs #unitedstates

Recalls BREXAFEMME® Antifungal oral medication - recalled due to Potential cross contamination SCYNEXIS, Inc... photo #1
312   Comments Comment

Recall notice

Novartis Sandimunne Oral Solution - recalled due to crystallization, USA

2 years ago •source fda.gov • details

Novartis is conducting a voluntary nationwide recall at the consumer level of one lot of its Sandimmune® Oral Solution (cyclosporine oral solution, USP), 100 mg/mL in the US due to crystal formation observed in some bottles, which could potentially result in incorrect dosing. This lot was distributed… See more

#recall #drugs #unitedstates

Recalls Novartis Sandimunne Oral Solution - recalled due to crystallization Novartis is conducting a volunta... photo #1
312   Comments Comment

Recall notice

TheraBreath Kids Strawberry Splash Oral Rinse - recalled due to microbial contamination, USA

2 years ago •source fda.gov • details

Church & Dwight Co., Inc. (NYSE:CHD) today initiated a voluntary recall of one specific lot of TheraBreath Kids Strawberry Splash 16oz after the Company identified a microbial contamination due to the presence of yeast (Candida Parapsilosis) in lot #PA3083011 of the product, sold exclusively on Amazon between… See more

#recall #drugs #unitedstates

Recalls TheraBreath Kids Strawberry Splash Oral Rinse - recalled due to microbial contamination Church & Dwi... photo #1
312   Comments Comment

Recall notice

Costa sandwich and wrap products - recall due to the presence of small stones, UK

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

Costa is recalling several sandwich and wrap products because they may contain small stones. This may present a choking hazard and are unsafe to eat. This product was recalled in the United Kingdom.

-Product details
Costa Chicken & Bacon Caesar Wrap, Pack size: (192g), Use by: 06… See more

#recall #unitedkingdom

Recalls Costa sandwich and wrap products - recall due to the presence of small stones Costa is recalling sev... photo #1
158   Comments Comment

Recall notice

NUT DIET MAX Nuez de la India Seeds and Capsules - recalled due to health risk-contain cardiac glycosides, USA

2 years ago •source fda.gov • details

OBC GROUP CORP of, Miami, FL is recalling its NUT DIET MAX Nuez de la India Seeds and Capsules because FDA analysis has determined that the products appear to be Thevetia peruviana, or yellow oleander. The product NUEZ DE LA INDIA Seeds was distributed online through Amazon… See more

#vitamins #amazon #walmart #recall #unitedstates

Recalls NUT DIET MAX Nuez de la India Seeds and Capsules - recalled due to health risk-contain cardiac glyco... photo #1
312   Comments Comment

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