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Drugs

Updated:

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

5 months ago •source www.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
303

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

6 months ago •source www.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
303

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

6 months ago •source www.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
303

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

6 months ago •source www.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
303

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

6 months ago •source www.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
303

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

7 months ago •source www.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
303

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

7 months ago •source www.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

#recall #drugs #us

KVK-Tech Betaxolol Tablets, USP - recalled due to Potential Presence of Oxycodone HCl tablet photo #1
303

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

7 months ago •source www.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

#blood #recall #drugs #us

Hospira Sodium Bicarbonate & Lidocaine HCl Injections - recalled due to potential presence of glass particulate matter photo #1
303

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

7 months ago •source www.fda.gov • details

Recall notice

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 #us

Ion & Restore brands Nasal Sprays - recalled due to due to Microbial Contamination photo #1
303

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

7 months ago •source www.fda.gov • details

Recall notice

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

#drugs #recall #us

Merck Animal Health Banamine/Banamine-S Update - recalled due to presence of particulate matter photo #1
303

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