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Safety Reports: Drugs

Updated: November 21, 2023 9:02 AM

Real Time Reports

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

1 year 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

#drugs #recall #dietarysupplements #unitedstates

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

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

1 year 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

#drugs #recall #unitedstates

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

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

1 year 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

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

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

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

1 year 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

#drugs #recall #unitedstates

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

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

1 year 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

#drugs #recall #unitedstates

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

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

1 year 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

#drugs #recall #unitedstates

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

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

1 year 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

#dietarysupplements #recall #drugs #unitedstates

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

1 year 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

#familydollar #recall #drugs #medicaldevices #unitedstates

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

1 year ago •source fda.gov • details

Recall notice

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

#drugs #recall #unitedstates

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

1 year ago •source fda.gov • details

Recall notice

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

#drugs #recall #blood #unitedstates

Hospira Sodium Bicarbonate & Lidocaine HCl Injections - recalled due to potential presence of glass particulate matter photo #1

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Safety Reports: Drugs

Real Time Reports

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

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

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

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

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

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

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

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

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

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

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