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Safety Reports: Drugs

Updated:

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

6 months ago •source fda.gov • details

Recall notice

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

#recall #drugs #us

TING® 2% Miconazole Nitrate Athlete’s Foot Spray Antifungal SprayPowder - recalled due to the presence of benzene photo #1
322

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

6 months ago •source fda.gov • details

Recall notice

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

#recall #drugs #us

Bayer Vitrakvi (larotrectinib) Oral Solution - recalled due to microbial contamination photo #1
321

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

6 months ago •source fda.gov • details

Recall notice

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

#dietarysupplements #recall #drugs #us

Noah’s Wholesale, LLC Dietary Supplement - recalled due to undeclared Sildenafil photo #1
321

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

6 months ago •source fda.gov • details

Recall notice

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

#recall #drugs #us

KinderMed OTC Pain and Fever Reliever for Infants and Kids - recalled due to Acetaminophen Instability photo #1
321

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

7 months ago •source fda.gov • details

Recall notice

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

#cvspharmacy #recall #target #walmart #drugs #us

Kilitch Healthcare India Limited Lubricant Eye Drops & Multi-Symptom Eye Drops - recalled due to insanitary conditions photo #1
321

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

7 months ago •source fda.gov • details

Recall notice

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 #us

Rugby OTC Ophthalmic Sterile Drops - recalled due to Insanitary manufacturing conditions photo #1
321

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

7 months ago •source fda.gov • details

Recall notice

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 #us

LEADER OTC Ophthalmic Sterile Drops - recalled due to Insanitary manufacturing conditions photo #1
321

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

7 months ago •source fda.gov • details

Recall notice

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 #us

Exela & Civica injection products - recalled due to particulate matter presence photo #1
321

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

7 months ago •source fda.gov • details

Recall notice

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

#drugs #recall #dietarysupplements #us

Botanical-Be Dietary Supplements - recalled due to Undeclared Diclofenac photo #1
321

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

8 months ago •source fda.gov • details

Recall notice

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 #us

Family Dollar Over-the-Counter Drug & Medical Device products - recalled due to improper storage temperature photo #1
321

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