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Safety Reports: Drugs

Updated:

Real Time Reports

Recall notice

Novartis Sandimmune Oral Solution - recalled due to due to crystallization formation, USA

2 years ago •source fda.gov • details

Novartis is conducting a voluntary nationwide recall at the consumer level of two lots 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. The issue was identified… See more

#drugs #recall #unitedstates

Recalls Novartis Sandimmune Oral Solution - recalled due to due to crystallization formation Novartis is con... photo #1
312   Comments Comment

Recall notice

TING® 2% Miconazole Nitrate Athlete's Foot Spray Antifungal SprayPowder - recalled due to the presence of benzene, USA

2 years ago •source fda.gov • details

Insight Pharmaceuticals, a Prestige Consumer Healthcare Inc. company ("Insight"), is voluntarily recalling two lots of TING® 2% Miconazole Nitrate Athlete's Foot Spray Antifungal Spray Powder to the consumer level. A recent review by our manufacturer and their third-party lab found that samples from two lots of the… See more

#drugs #recall #unitedstates

Recalls TING® 2% Miconazole Nitrate Athlete’s Foot Spray Antifungal SprayPowder - recalled due to the presen... photo #1
313   Comments Comment

Recall notice

Bayer Vitrakvi (larotrectinib) Oral Solution - recalled due to microbial contamination, USA

2 years ago •source fda.gov • details

Bayer is voluntarily recalling one lot of Vitrakvi® (larotrectinib) Oral Solution 20 mg/mL in 100mL glass bottles to the consumer/user level. The product is being recalled due to microbial contamination identified as Penicillium brevicompactum observed during routine ongoing stability testing. It was distributed to wholesale distributors and… See more

#drugs #recall #unitedstates

Recalls Bayer Vitrakvi (larotrectinib) Oral Solution - recalled due to microbial contamination Bayer is volu... photo #1
312   Comments Comment

Recall notice

Noah's Wholesale, LLC Dietary Supplement - recalled due to undeclared Sildenafil, USA

2 years ago •source fda.gov • details

Noah's Wholesale, LLC is voluntarily recalling one lot of rock# 03032021, exp:12/2027, 1200 mg/capsule, to the consumer level. FDA analysis has found the product to be tainted with Sildenafil. The product was distributed locally through convenience stores and some island jobbers (small wholesale distributors to retail). Noah's… See more

#vitamins #drugs #recall #dietarysupplements #supplement #unitedstates

Recalls Noah’s Wholesale, LLC Dietary Supplement - recalled due to undeclared Sildenafil Noah’s Wholesale,... photo #1
312   Comments Comment

Recall notice

KinderMed OTC Pain and Fever Reliever for Infants and Kids - recalled due to Acetaminophen Instability, USA

2 years ago •source fda.gov • details

KinderFarms, LLC is voluntarily recalling all lots of KinderMed Infants' Pain & Fever (oral suspension) and KinderMed Kids' Pain & Fever (oral suspension) to the retail and consumer level. These products are being voluntarily recalled due to acetaminophen instability. These products are available nationwide in drug/pharmacy, supermarkets,… See more

#drugs #recall #unitedstates

Recalls KinderMed OTC Pain and Fever Reliever for Infants and Kids - recalled due to Acetaminophen Instabili... photo #1
312   Comments Comment

Recall notice

Kilitch Healthcare India Limited Lubricant Eye Drops & Multi-Symptom Eye Drops - recalled due to insanitary conditions, USA

2 years ago •source fda.gov • details

Kilitch Healthcare India Limited is voluntarily recalling the eye drops products to the consumer level with all lots within expiry with expiration dates ranging from November, 2023 to September, 2025 for all the below mentioned products. These products are being recalled due to potential safety concerns after… See more

#recall #walmart #cvspharmacy #target #drugs #unitedstates

Recalls Kilitch Healthcare India Limited Lubricant Eye Drops & Multi-Symptom Eye Drops - recalled due to ins... photo #1
312   Comments Comment

Recall notice

Rugby OTC Ophthalmic Sterile Drops - recalled due to Insanitary manufacturing conditions, USA

2 years ago •source fda.gov • details

The Harvard Drug Group, LLC d/b/a Major® Pharmaceutical and Rugby® Laboratories is initiating a voluntarily recall for all lots of Polyvinyl Alcohol, 1.4% Lubricating Eye Drops and Lubricating Tears Eye Drops (Dextran/Hypromellose, 0.1%/0.3%) supplied by Velocity Pharma, LLC to the consumer level. The Harvard Drug Group, LLC… See more

#recall #drugs #unitedstates

Recalls Rugby OTC Ophthalmic Sterile Drops - recalled due to Insanitary manufacturing conditions The Harvard... photo #1
312   Comments Comment

Recall notice

LEADER OTC Ophthalmic Sterile Drops - recalled due to Insanitary manufacturing conditions, USA

2 years ago •source fda.gov • details

Cardinal Health, Inc. is initiating a voluntarily recall for all lots of ophthalmic products supplied by Velocity Pharma, LLC to the consumer level. Cardinal Health, Inc. received information from FDA indicating investigators found insanitary conditions in the manufacturing facility and positive bacterial test results from environmental sampling… See more

#recall #drugs #unitedstates

Recalls LEADER OTC Ophthalmic Sterile Drops - recalled due to Insanitary manufacturing conditions Cardinal H... photo #1
312   Comments Comment

Recall notice

Exela & Civica injection products - recalled due to particulate matter presence, USA

2 years ago •source fda.gov • details

Lenoir, North Carolina. Exela Pharma Sciences, LLC, (Exela) is voluntarily recalling several products to the consumer level because particulate matter identified as silicone was observed during routine inspection of retain samples. Exela has not received any reports of adverse events related to this recall. These products were… See more

#recall #drugs #unitedstates

Recalls Exela & Civica injection products - recalled due to particulate matter presence Lenoir, North Caroli... photo #1
312   Comments Comment

Recall notice

Botanical-Be Dietary Supplements - recalled due to Undeclared Diclofenac, USA

2 years ago •source fda.gov • details

Botanical-Be is voluntarily recalling all lots of Kuka Flex Forte, Capsules, Artri King, Capsules, and Reumo Flex, Capsules to the consumer level. FDA analysis has found these capsules, to be tainted with Diclofenac. Diclofenac is an approved non-steroidal anti-inflammatory drug (NSAID), the presence of Diclofenac in Kuka… See more

#vitamins #supplement #drugs #recall #dietarysupplements #unitedstates

Recalls Botanical-Be Dietary Supplements - recalled due to Undeclared Diclofenac Botanical-Be is voluntarily... photo #1
312   Comments Comment

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