Search Results for Nationwide recall
Showing results 901 - 920 of 975 for Nationwide recall.
California Popsicle, Inc. Issues Allergy Alert on Undeclared Milk in Ice Bars | FDA
This recall has been completed and FDA has terminated this recall....Bars This recall has been completed and FDA has terminated this recall. When a...a company announces a recall, market withdrawal, or safety alert, the FDA posts
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/california-popsicle-inc-issues-allergy-alert-undeclared-milk-ice-bars
Advocare Issues Allergy Alert in Select Bottles of Muscle Strength and Nighttime Recovery Product Because of Undeclared Milk Allergen on The Label | FDA
This recall has been completed and FDA has terminated this recall....Label This recall has been completed and FDA has terminated this recall. When a...a company announces a recall, market withdrawal, or safety alert, the FDA posts
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/advocare-issues-allergy-alert-select-bottles-muscle-strength-and-nighttime-recovery-product-because
Lotte Int’l America Corp Issues Allergy Alert on Undeclared Peanut In "Kancho Choco Biscuit" | FDA
This recall has been completed and FDA has terminated this recall....Biscuit" This recall has been completed and FDA has terminated this recall. When a...a company announces a recall, market withdrawal, or safety alert, the FDA posts
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/lotte-intl-america-corp-issues-allergy-alert-undeclared-peanut-kancho-choco-biscuit
Chun Yuen Trading Co. Issues Allergy Alert On Undeclared Milk | FDA
This recall has been completed and FDA has terminated this recall....Milk This recall has been completed and FDA has terminated this recall. When a...a company announces a recall, market withdrawal, or safety alert, the FDA posts
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/chun-yuen-trading-co-issues-allergy-alert-undeclared-milk
Wellements LLC Issues Allergy Alert On Undeclared Milk Allergen In Two Lots Of Iron Drops And Iron Drops Sample | FDA
Scottsdale, Arizona, is issuing a voluntary recall of two lots of its 1oz/30ml bottle...Sample When a company announces a recall, market withdrawal, or safety alert...Announcement View Product Photos More Recalls, Market Withdrawals, & Safety Alerts
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/wellements-llc-issues-allergy-alert-undeclared-milk-allergen-two-lots-iron-drops-and-iron-drops
Virginia Diner, Inc. Issues Allergy Alert on Undeclared Peanut Allergen in Chocolate Covered Cashews 10 oz. cans | FDA
This recall has been completed and FDA has terminated this recall....cans This recall has been completed and FDA has terminated this recall. When a...a company announces a recall, market withdrawal, or safety alert, the FDA posts
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/virginia-diner-inc-issues-allergy-alert-undeclared-peanut-allergen-chocolate-covered-cashews-10-oz
Herbal Doctor Remedies Issues Voluntary Nationwide Recall of All Drug Products Due to Marketing Without FDA Approval and Concerns with Manufacturing Practices | FDA
Herbal Doctor Remedies is voluntarily recalling all drug products (see table below)...Doctor Remedies Issues Voluntary Nationwide Recall of All Drug Products Due to Marketing...with Manufacturing Practices More Recalls, Market Withdrawals, & Safety Alerts
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/herbal-doctor-remedies-issues-voluntary-nationwide-recall-all-drug-products-due-marketing-without
Apotex Corp. Issues Voluntary Nationwide Recall of Drospirenone and Ethinyl Estradiol Tablets, USP, 28x3 Blister Pack/Carton Due to Possibility of Missing/Incorrect Tablet Arrangement | FDA
Florida, Apotex Corp. is voluntarily recalling four lots of Drospirenone and Ethinyl...the patient /user level. The four recalled lots of Drospirenone and Ethinyl Estradiol...Apotex Corp. Issues Voluntary Nationwide Recall of Drospirenone and Ethinyl Estradiol...Arrangement When a company announces a recall, market withdrawal, or safety alert
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/apotex-corp-issues-voluntary-nationwide-recall-drospirenone-and-ethinyl-estradiol-tablets-usp-28x3
Apotex Corp. Issues Voluntary Nationwide Recall of Ranitidine Tablets 75mg and 150mg (All pack sizes and Formats) due to the potential for Detection of an Amount of Unexpected Impurity,N-nitrosodimethylamine (NDMA) Impurity in the product | FDA
...voluntarily, on a precautionary basis, recalling Ranitidine Tablets 75mg and 150mg...Apotex Corp. Issues Voluntary Nationwide Recall of Ranitidine Tablets 75mg and...product When a company announces a recall, market withdrawal, or safety alert
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/apotex-corp-issues-voluntary-nationwide-recall-ranitidine-tablets-75mg-and-150mg-all-pack-sizes-and
Amneal Pharmaceuticals, LLC. Issues Voluntary Nationwide Recall of Ranitidine Tablets, USP, 150mg and 300mg, and Ranitidine Syrup (Ranitidine Oral Solution, USP), 15 mg/mL, Due to Possible Presence of N-nitrosodimethylamine (NDMA) Impurity | FDA
Bridgewater, New Jersey is voluntarily recalling Ranitidine Tablets, 150 mg and 300...consumer level. A listing of the recalled lots is identified below. Ranitidine...Pharmaceuticals, LLC. Issues Voluntary Nationwide Recall of Ranitidine Tablets, USP, 150mg...Impurity When a company announces a recall, market withdrawal, or safety alert
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/amneal-pharmaceuticals-llc-issues-voluntary-nationwide-recall-ranitidine-tablets-usp-150mg-and-300mg
Promise Pharmacy Issues Voluntary Nationwide Recall of Prednisolone and Gatifloxacin Ophthalmic Solution 1%/0.5% Sterile Due to Small Particulate Floating in the Solution | FDA
Promise Pharmacy is voluntarily recalling one lot of Prednisolone and Gatifloxacin...Promise Pharmacy Issues Voluntary Nationwide Recall of Prednisolone and Gatifloxacin...Solution When a company announces a recall, market withdrawal, or safety alert
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/promise-pharmacy-issues-voluntary-nationwide-recall-prednisolone-and-gatifloxacin-ophthalmic
Living Well Remedies, LLC Issues Voluntary Nationwide Recall of Weight Away Remedy, Lot # 111417LWL614, Due To Microbial Contamination | FDA
Well Remedies, LLC is voluntarily recalling Weight Away Remedy lot# 111417LWL614...Remedies, LLC Issues Voluntary Nationwide Recall of Weight Away Remedy, Lot #...Contamination When a company announces a recall, market withdrawal, or safety alert
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/living-well-remedies-llc-issues-voluntary-nationwide-recall-weight-away-remedy-lot-111417lwl614-due
Product Quest Manufacturing LLC Issues Voluntary Nationwide Recall of CVS Health 12 Hour Sinus Relief Nasal Mist Due to Microbiological Contamination | FDA
...(“Product Quest”) is voluntarily recalling Lot# 173089J of CVS Health 12 Hour...Manufacturing LLC Issues Voluntary Nationwide Recall of CVS Health 12 Hour Sinus Relief...Agency Partner announces a company’s recall, market withdrawal, or safety alert
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/product-quest-manufacturing-llc-issues-voluntary-nationwide-recall-cvs-health-12-hour-sinus-relief
B&G Foods Issues Voluntary Allergy Alert on Undeclared Milk in a Limited Number of Boxes of Back to Nature® Organic Rosemary & Olive Oil Stoneground Wheat Crackers | FDA
...announced today it is voluntarily recalling 1,502 cases of a single date code...Crackers When a company announces a recall, market withdrawal, or safety alert...Announcement View Product Photos More Recalls, Market Withdrawals, & Safety Alerts
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/bg-foods-issues-voluntary-allergy-alert-undeclared-milk-limited-number-boxes-back-naturer-organic
Pfizer Inc. Issues A Voluntary Nationwide Consumer Level Recall of Six Lots of Thermacare® Heatwraps Due to Leaking Wraps With The Potential For Skin Injuries | FDA
...division of Pfizer Inc., is voluntarily recalling six lots of ThermaCare® HeatWrap...Consumer Healthcare initiated this recall because product from these lots has...Inc. Issues A Voluntary Nationwide Consumer Level Recall of Six Lots of Thermacare®...Injuries When a company announces a recall, market withdrawal, or safety alert
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/pfizer-inc-issues-voluntary-nationwide-consumer-level-recall-six-lots-thermacarer-heatwraps-due
Infusion Options Inc. Issues Voluntary Nationwide Recall of All Lots of All Sterile Products Due to Lack of Assurance of Sterility | FDA
Infusion Options Inc. is voluntarily recalling all lots of all sterile products...hospital level. These products are being recalled due to a lack of assurance of sterility...Options Inc. Issues Voluntary Nationwide Recall of All Lots of All Sterile Products...Sterility When a company announces a recall, market withdrawal, or safety alert
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/infusion-options-inc-issues-voluntary-nationwide-recall-all-lots-all-sterile-products-due-lack
KRS Global Biotechnology, Inc. Issues Voluntary Nationwide Recall of All Human and Animal Sterile Drug Products Due to Lack of Assurance of Sterility | FDA
Biotechnology, Inc. is voluntarily recalling all lots of unexpired human and animal...consumer level. The products are being recalled due to lack of assurance of sterility...Biotechnology, Inc. Issues Voluntary Nationwide Recall of All Human and Animal Sterile...Sterility When a company announces a recall, market withdrawal, or safety alert
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/krs-global-biotechnology-inc-issues-voluntary-nationwide-recall-all-human-and-animal-sterile-drug
Stokes Healthcare Inc. Issues Voluntary Nationwide Recall of Pilocarpine 0.1% Ophthalmic Solution Due to a High Level of Preservative | FDA
Stokes Healthcare Inc. is voluntarily recalling 1 lot of 81 units of Pilocarpine...Healthcare Inc. Issues Voluntary Nationwide Recall of Pilocarpine 0.1% Ophthalmic...Preservative When a company announces a recall, market withdrawal, or safety alert
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/stokes-healthcare-inc-issues-voluntary-nationwide-recall-pilocarpine-01-ophthalmic-solution-due-high
Hospira Issues a Voluntary Nationwide Recall For One Lot Of 25% Dextrose Injection, USP (Infant) Due To The Presence of Particulate Matter | FDA
...a Pfizer company, is voluntarily recalling one lot of 25% Dextrose Injection...ANNOUNCEMENT Hospira Issues a Voluntary Nationwide Recall For One Lot Of 25% Dextrose Injection...Matter When a company announces a recall, market withdrawal, or safety alert
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/hospira-issues-voluntary-nationwide-recall-one-lot-25-dextrose-injection-usp-infant-due-presence
ICU Medical Issues a Voluntary Nationwide Recall of Certain Lots of ChemoLock™ and ChemoClave® Vial Spikes Due to the Potential for Burr Particulate | FDA
... Inc. today announced a voluntary recall of certain lots of ChemoLock™ and ChemoClave®...ICU Medical Issues a Voluntary Nationwide Recall of Certain Lots of ChemoLock™...Particulate When a company announces a recall, market withdrawal, or safety alert
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/icu-medical-issues-voluntary-nationwide-recall-certain-lots-chemolocktm-and-chemoclaver-vial-spikes