Search Results for Nationwide recall
Showing results 101 - 120 of 975 for Nationwide recall.
Boulla LLC Issues Voluntary Nationwide Recall of ZoomMax and ZapMax Capsules Due to the Presence of Undeclared Sildenafil and Diclofenac | FDA
Sacramento, CA, Boulla LLC is voluntarily recalling lot YZM240406, Exp 04/05/27, of ZoomMax...ANNOUNCEMENT Boulla LLC Issues Voluntary Nationwide Recall of ZoomMax and ZapMax Capsules...Diclofenac When a company announces a recall, market withdrawal, or safety alert
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/boulla-llc-issues-voluntary-nationwide-recall-zoommax-and-zapmax-capsules-due-presence-undeclared
Asiaticon SA de CV Issues Voluntary Nationwide Recall of V-Klean Hand Sanitizer Gel, Medically Minded Hand Sanitizer Gel and Protz Real Protection Antibacterial Hand Sanitizer Due to Potential Presence of Methanol (Wood Alcohol) and Subpotent Ethanol Levels | FDA
This recall has been completed and FDA has terminated this recall....Asiaticon SA de CV Issues Voluntary Nationwide Recall of V-Klean Hand Sanitizer Gel...Levels This recall has been completed and FDA has terminated this recall. When a
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/asiaticon-sa-de-cv-issues-voluntary-nationwide-recall-v-klean-hand-sanitizer-gel-medically-minded
Par Pharmaceutical Issues Voluntary Nationwide Recall of One Lot of Treprostinil Injection Due to Potential for Silicone Particulates in the Product Solution | FDA
Pharmaceutical, Inc. (Par), is voluntarily recalling one lot of Treprostinil Injection...consumer level. The product is being recalled due to the potential for the presence...Pharmaceutical Issues Voluntary Nationwide Recall of One Lot of Treprostinil Injection...Solution When a company announces a recall, market withdrawal, or safety alert
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/par-pharmaceutical-issues-voluntary-nationwide-recall-one-lot-treprostinil-injection-due-potential
Pfizer Issues a Voluntary Nationwide Recall for Twelve Lots of CHANTIX® (Varenicline) Tablets Due to N-Nitroso Varenicline Content | FDA
Pfizer is voluntarily recalling two lots of Chantix 0.5mg Tablets, two lots...ANNOUNCEMENT Pfizer Issues a Voluntary Nationwide Recall for Twelve Lots of CHANTIX® (Varenicline)...Content When a company announces a recall, market withdrawal, or safety alert
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/pfizer-issues-voluntary-nationwide-recall-twelve-lots-chantixr-varenicline-tablets-due-n-nitroso
Kilitch Healthcare India Limited Issues Voluntary Nationwide Recall of Various Eye Drops for Potential Safety Reasons | FDA
Healthcare India Limited is voluntarily recalling the eye drops products listed in...India Limited Issues Voluntary Nationwide Recall of Various Eye Drops for Potential...Reasons When a company announces a recall, market withdrawal, or safety alert
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/kilitch-healthcare-india-limited-issues-voluntary-nationwide-recall-various-eye-drops-potential
Hospira Inc. Issues A Voluntary Nationwide Recall For Buprenorphine Hydrochloride Injection CarpujectTM Units and Labetalol Hydrochloride Injection, USP CarpujectTM Units Due to the Potential for Incomplete Crimp Seals | FDA
...company (“Pfizer”), is voluntarily recalling the lots listed in the table below...CarpujectTM Units to the User level. The recall was initiated due to the potential...Hospira Inc. Issues A Voluntary Nationwide Recall For Buprenorphine Hydrochloride...Crimp Seals When a company announces a recall, market withdrawal, or safety alert
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/hospira-inc-issues-voluntary-nationwide-recall-buprenorphine-hydrochloride-injection-carpujecttm
HomeoCare Laboratories Inc. Issues Voluntary Nationwide Recall of Homeopathic Stella Life Oral Care Spray Unflavored and Advanced Formula Peppermint Oral Care Rinse Due to Microbial Contamination | FDA
...homeopathic products, is voluntarily recalling two batches of Homeopathic StellaLife...findings of microbial contamination. This recall is to be performed at the consumer...Laboratories Inc. Issues Voluntary Nationwide Recall of Homeopathic Stella Life Oral...Contamination When a company announces a recall, market withdrawal, or safety alert
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/homeocare-laboratories-inc-issues-voluntary-nationwide-recall-homeopathic-stella-life-oral-care
Pfizer Expands Voluntary Nationwide Recall to include All Lots of CHANTIX® (Varenicline) Tablets Due to N-Nitroso Varenicline Content | FDA
Pfizer is voluntarily recalling all lots of Chantix 0.5 mg and 1 mg Tablets...ANNOUNCEMENT Pfizer Expands Voluntary Nationwide Recall to include All Lots of CHANTIX®...Content When a company announces a recall, market withdrawal, or safety alert
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/pfizer-expands-voluntary-nationwide-recall-include-all-lots-chantixr-varenicline-tablets-due-n
123Herbals LLC (123Herbals.com) Issues Voluntary Nationwide Recall of Vail-Bon Jie Yang Wan Capsules Due to the Presence of Undeclared Dexamethasone and Chlorpheniramine | FDA
Rosemead, CA, 123herbals is voluntarily recalling all lots of Vail-Bon Jie Yang Wan...(123Herbals.com) Issues Voluntary Nationwide Recall of Vail-Bon Jie Yang Wan Capsules...Chlorpheniramine When a company announces a recall, market withdrawal, or safety alert
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/123herbals-llc-123herbalscom-issues-voluntary-nationwide-recall-vail-bon-jie-yang-wan-capsules-due
Marksans Pharma Limited Issues Expansion of Voluntary Nationwide Recall of Metformin Hydrochloride Extended-Release Tablets, USP 500mg & 750mg, Due to the Detection of N-Nitrosodimethylamine (NDMA) | FDA
This recall has been completed and FDA has terminated this recall....Issues Expansion of Voluntary Nationwide Recall of Metformin Hydrochloride Extended-Release...(NDMA) This recall has been completed and FDA has terminated this recall. When a
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/marksans-pharma-limited-issues-expansion-voluntary-nationwide-recall-metformin-hydrochloride
Yamtun7 Issues Voluntary Nationwide Recall of Poseidon Platinum 3500 Due to the Presence of Undeclared Tadalafil and Sildenafil | FDA
This recall has been completed and FDA has terminated this recall....ANNOUNCEMENT Yamtun7 Issues Voluntary Nationwide Recall of Poseidon Platinum 3500 Due...Sildenafil This recall has been completed and FDA has terminated this recall. When a
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/yamtun7-issues-voluntary-nationwide-recall-poseidon-platinum-3500-due-presence-undeclared-tadalafil
Staska Pharmaceuticals, Inc. Issues Voluntary Nationwide Recall of Ascorbic Acid Solution for Injection (Preservative Free, Non-Corn) 500mg/mL Due to the Presence of Glass Particles | FDA
PHARMACEUTICALS, INC. is voluntarily recalling 1 lot of Ascorbic Acid Solution for...Pharmaceuticals, Inc. Issues Voluntary Nationwide Recall of Ascorbic Acid Solution for...Particles When a company announces a recall, market withdrawal, or safety alert
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/staska-pharmaceuticals-inc-issues-voluntary-nationwide-recall-ascorbic-acid-solution-injection
Magno-Humphries Laboratories, Inc., Issues Voluntary Nationwide Recall of Basic Drugs Brand of Senna Laxative Due to Mislabeling | FDA
This recall has been completed and FDA has terminated this recall....Laboratories, Inc., Issues Voluntary Nationwide Recall of Basic Drugs Brand of Senna...Mislabeling This recall has been completed and FDA has terminated this recall. When a
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/magno-humphries-laboratories-inc-issues-voluntary-nationwide-recall-basic-drugs-brand-senna-laxative
American Health Packaging on Behalf of BluePoint Laboratories Issues Voluntary Nationwide Recall for Potassium Chloride Extended-Release Capsules, USP (750 mg) 10 mEq K Due to Failed Dissolution | FDA
BluePoint Laboratories is voluntarily recalling 21 batches of Potassium Chloride...consumer level. The product is being recalled because of failed dissolution.Risk...Laboratories Issues Voluntary Nationwide Recall for Potassium Chloride Extended-Release...Dissolution When a company announces a recall, market withdrawal, or safety alert
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/american-health-packaging-behalf-bluepoint-laboratories-issues-voluntary-nationwide-recall-potassium
Bayer Issues Voluntary Recall Nationwide of VITRAKVI® (larotrectinib) Oral Solution 20 mg/mL Due to Presence of Microbial Contamination | FDA
Bayer is voluntarily recalling one lot of Vitrakvi® (larotrectinib) Oral Solution...consumer/user level. The product is being recalled due to microbial contamination identified...ANNOUNCEMENT Bayer Issues Voluntary Recall Nationwide of VITRAKVI® (larotrectinib)...Contamination When a company announces a recall, market withdrawal, or safety alert
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/bayer-issues-voluntary-recall-nationwide-vitrakvir-larotrectinib-oral-solution-20-mgml-due-presence
Buy-herbal.com Issues Voluntary Nationwide Recall of Nhan Sam Tuyet Lien Truy Phong Hoan Capsules Due to Undeclared Furosemide, Dexamethasone and Chlorpheniramine | FDA
York, Buy-herbal.com is voluntarily recalling all lots within expiry of Nhan Sam...Buy-herbal.com Issues Voluntary Nationwide Recall of Nhan Sam Tuyet Lien Truy Phong...Chlorpheniramine When a company announces a recall, market withdrawal, or safety alert
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/buy-herbalcom-issues-voluntary-nationwide-recall-nhan-sam-tuyet-lien-truy-phong-hoan-capsules-due
Gilead Issues Voluntary Nationwide Recall of One Lot of Veklury (Remdesivir) for Injection 100 mg/vial Due to the Presence of a Glass Particle | FDA
...announced it is issuing a voluntary recall of one lot of Veklury® (remdesivir)...ANNOUNCEMENT Gilead Issues Voluntary Nationwide Recall of One Lot of Veklury (Remdesivir)...Particle When a company announces a recall, market withdrawal, or safety alert
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/gilead-issues-voluntary-nationwide-recall-one-lot-veklury-remdesivir-injection-100-mgvial-due
Bryant Ranch Prepack Inc. Issues Voluntary Nationwide Recall of Morphine Sulfate 30 mg Extended Release and Morphine Sulfate 60 mg Extended-Release Due to Label-Mix Up | FDA
This recall has been completed and FDA has terminated this recall....Prepack Inc. Issues Voluntary Nationwide Recall of Morphine Sulfate 30 mg Extended...Up This recall has been completed and FDA has terminated this recall. When a
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/bryant-ranch-prepack-inc-issues-voluntary-nationwide-recall-morphine-sulfate-30-mg-extended-release
Vivimed Life Sciences Pvt Ltd Issues Voluntary Nationwide Recall of Losartan Potassium 25 mg, 50 mg and 100 mg Tablets, USP Due to the Detection of Trace Amounts of N-Nitroso-N-methyl-4-aminobutyric acid (NMBA) Impurity | FDA
This recall has been completed and FDA has terminated this recall....Sciences Pvt Ltd Issues Voluntary Nationwide Recall of Losartan Potassium 25 mg,...Impurity This recall has been completed and FDA has terminated this recall. When a
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/vivimed-life-sciences-pvt-ltd-issues-voluntary-nationwide-recall-losartan-potassium-25-mg-50-mg-and
B. Braun Issues Voluntary Nationwide Recall of 0.9% Sodium Chloride for Injection USP 1000 mL in E3 Containers Due to the Potential for Particulate Matter and Leakage | FDA
Medical Inc. (B. Braun), is voluntarily recalling two (2) lots of 0.9% Sodium Chloride...the consumer level. The voluntary recall has been initiated due to the potential...ANNOUNCEMENT B. Braun Issues Voluntary Nationwide Recall of 0.9% Sodium Chloride for Injection...Leakage When a company announces a recall, market withdrawal, or safety alert
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/b-braun-issues-voluntary-nationwide-recall-09-sodium-chloride-injection-usp-1000-ml-e3-containers