Search Results for Nationwide recall
Showing results 161 - 180 of 975 for Nationwide recall.
8th Avenue Pharmacy Issues Voluntary Nationwide Recall of Notoginseng Formula Special Gout Granule Due to the Presence of Hidden Drug Ingredients, Diclofenac and Dexamethasone | FDA
...8th Avenue Pharmacy is voluntarily recalling all lots within expiry of Notoginseng...Avenue Pharmacy Issues Voluntary Nationwide Recall of Notoginseng Formula Special...Dexamethasone When a company announces a recall, market withdrawal, or safety alert
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/8th-avenue-pharmacy-issues-voluntary-nationwide-recall-notoginseng-formula-special-gout-granule-due
Brassica Pharma Pvt. Ltd. Issues Voluntary Nationwide Recall of Equate Lubricant Eye Ointment, Equate Stye Lubricant Eye Ointment, CVS Health Lubricant Eye Ointment, Lubricant PM Ointment Due to Potential Lack of Sterility | FDA
Brassica Pharma Pvt. Ltd. is voluntarily recalling Eye Ointment products listed in the...September 2025. The products are being recalled due to lack of sterility assurance...Pharma Pvt. Ltd. Issues Voluntary Nationwide Recall of Equate Lubricant Eye Ointment...Sterility When a company announces a recall, market withdrawal, or safety alert
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/brassica-pharma-pvt-ltd-issues-voluntary-nationwide-recall-equate-lubricant-eye-ointment-equate-stye
Update to Palmer Candy Company Recall of White Confectionary Products Because of Possible Health Risk | FDA
The recalled confectionary items were distributed nationwide in Walmart, HyVee...ANNOUNCEMENT Update to Palmer Candy Company Recall of White Confectionary Products Because...Health Risk When a company announces a recall, market withdrawal, or safety alert
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/update-palmer-candy-company-recall-white-confectionary-products-because-possible-health-risk
ICU Medical Issues a Voluntary Nationwide Recall of Aminosyn II 15%, An Amino Acid Injection, Sulfite Free IV Solution Due to the Presence of Particulate Matter | FDA
This recall has been completed and FDA has terminated this recall....ICU Medical Issues a Voluntary Nationwide Recall of Aminosyn II 15%, An Amino...Matter This recall has been completed and FDA has terminated this recall. When a
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/icu-medical-issues-voluntary-nationwide-recall-aminosyn-ii-15-amino-acid-injection-sulfite-free-iv
Insight Pharmaceuticals Issues Voluntary Nationwide Recall of TING® 2% Miconazole Nitrate Athlete’s Foot Spray Antifungal Spray Powder Due to the Presence of Benzene | FDA
...company (“Insight”), is voluntarily recalling two lots of TING® 2% Miconazole Nitrate...Pharmaceuticals Issues Voluntary Nationwide Recall of TING® 2% Miconazole Nitrate...Benzene When a company announces a recall, market withdrawal, or safety alert
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/insight-pharmaceuticals-issues-voluntary-nationwide-recall-tingr-2-miconazole-nitrate-athletes-foot
Aurobindo Pharma USA, Inc. on Behalf of AuroHealth, Issues Voluntary Nationwide Recall of one (1) Lot of Healthy Living Over the Counter (OTC) Migraine Relief: Acetaminophen 250mg; Aspirin 250mg; Caffeine 65mg Tablets, Due to Missing Manufacturer Label | FDA
...behalf of AuroHealth, is voluntarily recalling one lot (refer table below) of Healthy...AuroHealth, Issues Voluntary Nationwide Recall of one (1) Lot of Healthy Living...Manufacturer Label When a company announces a recall, market withdrawal, or safety alert
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/aurobindo-pharma-usa-inc-behalf-aurohealth-issues-voluntary-nationwide-recall-one-1-lot-healthy
Grupo Asimex De Mexico Sa De CV Issues Voluntary Nationwide Recall of All Lots of Florence Morris Antiseptic Hand Sanitizer Due to Presence of Methanol (Wood Alcohol) and Sub-Potent Ethanol | FDA
...de Mexico SA de CV is voluntarily recalling all lots of FLORANCE MORRIS Antiseptic...Mexico Sa De CV Issues Voluntary Nationwide Recall of All Lots of Florence Morris...Ethanol When a company announces a recall, market withdrawal, or safety alert
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/grupo-asimex-de-mexico-sa-de-cv-issues-voluntary-nationwide-recall-all-lots-florence-morris
Today The World Issues Voluntary Nationwide Recall of All Lots of Arize Herbal Dietary Supplement Capsules Due to the Presence of Undeclared Nortadalafil | FDA
...“Today The World” is voluntarily recalling one lot of Arize Herbal Dietary Supplement...Today The World Issues Voluntary Nationwide Recall of All Lots of Arize Herbal Dietary...Nortadalafil When a company announces a recall, market withdrawal, or safety alert
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/today-world-issues-voluntary-nationwide-recall-all-lots-arize-herbal-dietary-supplement-capsules-due
Eugia US LLC (f/k/a AuroMedics Pharma LLC) Issues Voluntary Nationwide Recall of Methocarbamol Injection, USP 1000 mg/10 mL (100mg/mL) (Single Dose Vial) Due to Presence of White Particles | FDA
Pharma LLC) has initiated a voluntary recall of lot number 3MC23011 of Methocarbamol...Pharma LLC) Issues Voluntary Nationwide Recall of Methocarbamol Injection, USP...Particles When a company announces a recall, market withdrawal, or safety alert
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/eugia-us-llc-fka-auromedics-pharma-llc-issues-voluntary-nationwide-recall-methocarbamol-injection
International Laboratories, LLC Issues Voluntary Nationwide Recall of one (1) Lot of Clopidogrel Tablets USP, 75 mg packaged in bottles of 30 tablets Due to Mislabeling NDC # 54458-888-16; Lot # 117099A | FDA
This recall has been completed and FDA has terminated this recall....Laboratories, LLC Issues Voluntary Nationwide Recall of one (1) Lot of Clopidogrel...117099A This recall has been completed and FDA has terminated this recall. When a
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/international-laboratories-llc-issues-voluntary-nationwide-recall-one-1-lot-clopidogrel-tablets-usp
Dr. Reddy's Laboratories Continues its Voluntary Nationwide Recall of Levetiracetam in 0.54% Sodium Chloride Injection 1500mg/100mL Due to Mislabeling | FDA
This recall has been completed and FDA has terminated this recall....Laboratories Continues its Voluntary Nationwide Recall of Levetiracetam in 0.54% Sodium...Mislabeling This recall has been completed and FDA has terminated this recall. When a
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/dr-reddys-laboratories-continues-its-voluntary-nationwide-recall-levetiracetam-054-sodium-chloride
Viona Pharmaceuticals Inc., Issues Voluntary Nationwide Recall of Metformin HCl Extended- Release Tablets, USP 750 mg, Due to the Detection of N-Nitrosodimethylamine (NDMA) Impurity | FDA
This recall has been completed and FDA has terminated this recall....Pharmaceuticals Inc., Issues Voluntary Nationwide Recall of Metformin HCl Extended- Release...Impurity This recall has been completed and FDA has terminated this recall. When a
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/viona-pharmaceuticals-inc-issues-voluntary-nationwide-recall-metformin-hcl-extended-release-tablets-0
Aruba Aloe Balm N.V. Issues Voluntary Nationwide Recall of Aruba Aloe Hand Sanitizer Gel Alcohol 80% and Aruba Aloe Alcoholada Gel Due to Presence of Methanol | FDA
Aruba Aloe Balm N.V. is voluntarily recalling 40 lots of Aruba Aloe Hand Sanitizer...Aloe Balm N.V. Issues Voluntary Nationwide Recall of Aruba Aloe Hand Sanitizer...Methanol When a company announces a recall, market withdrawal, or safety alert
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/aruba-aloe-balm-nv-issues-voluntary-nationwide-recall-aruba-aloe-hand-sanitizer-gel-alcohol-80-and
Mylan Pharmaceuticals Inc., a Viatris Company, Conducting Voluntary Nationwide Recall of One Batch of Insulin Glargine (Insulin glargine-yfgn) Injection, 100 units/mL (U-100), Due to the Potential for a Missing Label in the Batch | FDA
This recall has been completed and FDA has terminated this recall....Company, Conducting Voluntary Nationwide Recall of One Batch of Insulin Glargine...Batch This recall has been completed and FDA has terminated this recall. When a
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/mylan-pharmaceuticals-inc-viatris-company-conducting-voluntary-nationwide-recall-one-batch-insulin
Hua Da Trading Inc dba Wefun Inc Issues Voluntary Nationwide Recall of WEFUN Capsules Due to Presence of Undeclared Sildenafil | FDA
New York, WEFUN Inc is voluntarily recalling 300 Boxes of WEFUN Capsules to the...dba Wefun Inc Issues Voluntary Nationwide Recall of WEFUN Capsules Due to Presence...Sildenafil When a company announces a recall, market withdrawal, or safety alert
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/hua-da-trading-inc-dba-wefun-inc-issues-voluntary-nationwide-recall-wefun-capsules-due-presence
Cardinal Health, Inc. Issues Voluntary Nationwide Recall of Certain LEADER™ Brand Eye Drops Supplied by Velocity Pharma, LLC Due to Potential Risk of Eye Infections | FDA
... Inc. is initiating a voluntarily recall for all lots of ophthalmic products...Health, Inc. Issues Voluntary Nationwide Recall of Certain LEADER™ Brand Eye...Infections When a company announces a recall, market withdrawal, or safety alert
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/cardinal-health-inc-issues-voluntary-nationwide-recall-certain-leadertm-brand-eye-drops-supplied
Kadesh Incorporation Issues Voluntary Nationwide Recall of Puriton Eye Relief Drops Due to Non-Sterile Production Conditions | FDA
This recall has been completed and FDA has terminated this recall....Incorporation Issues Voluntary Nationwide Recall of Puriton Eye Relief Drops Due...Conditions This recall has been completed and FDA has terminated this recall. When a
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/kadesh-incorporation-issues-voluntary-nationwide-recall-puriton-eye-relief-drops-due-non-sterile
Today The World Issues Voluntary Nationwide Recall of All Lots of Sustain and Schwinnng brand Dietary Supplement Capsules Due to the Presence of Undeclared Tadalafil and Nortadalafil | FDA
...“Today The World” is voluntarily recalling two lots of Sustain herbal dietary...Today The World Issues Voluntary Nationwide Recall of All Lots of Sustain and Schwinnng...Nortadalafil When a company announces a recall, market withdrawal, or safety alert
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/today-world-issues-voluntary-nationwide-recall-all-lots-sustain-and-schwinnng-brand-dietary
Biomic Sciences Issues Voluntary Nationwide Recall of ION* Sinus Support, ION* Sinus, and Restore Sinus Spray Products Due to Microbial Contamination | FDA
...- Biomic Sciences is voluntarily recalling all lots of ION* Sinus Support, ION*...Biomic Sciences Issues Voluntary Nationwide Recall of ION* Sinus Support, ION* Sinus...Contamination When a company announces a recall, market withdrawal, or safety alert
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/biomic-sciences-issues-voluntary-nationwide-recall-ion-sinus-support-ion-sinus-and-restore-sinus
ForeverMen Supplements Recalled | FDA
This recall has been completed and FDA has terminated this recall....ANNOUNCEMENT ForeverMen Supplements Recalled This recall has been completed and FDA has...has terminated this recall. When a company announces a recall, market withdrawal
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/forevermen-supplements-recalled