Search Results for Nationwide recall
Showing results 941 - 960 of 975 for Nationwide recall.
Sandoz Inc. Issues Voluntary Nationwide Recall of One Lot of Losartan Potassium and Hydrochlorothiazide Due to the Detection of Trace Amounts of NDEA (N-Nitrosodiethylamine) Impurity Found in the Active Pharmaceutical Ingredient (API) | FDA
This product is being recalled due to the trace amount of an impurity, N-nitrosodiethylamine...Sandoz Inc. Issues Voluntary Nationwide Recall of One Lot of Losartan Potassium...Ingredient (API) When a company announces a recall, market withdrawal, or safety alert
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/sandoz-inc-issues-voluntary-nationwide-recall-one-lot-losartan-potassium-and-hydrochlorothiazide-due
Pfizer Inc. Issues A Voluntary Nationwide Consumer Level Recall of One Lot of ThermaCare® Back Pain Therapy HeatWraps, up to 16HR pain relief, Due To Out of Specification Results for High Cell Temperature | FDA
...division of Pfizer Inc., is voluntarily recalling one lot of ThermaCare® Back Pain...Inc. Issues A Voluntary Nationwide Consumer Level Recall of One Lot of ThermaCare®...Temperature 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-one-lot-thermacarer-back-pain-therapy
AurobindoPharma USA, Inc. Initiates a Voluntary Nationwide Consumer Level Recall Expansion of 38 Lots of Amlodipine Valsartan Tablets USP and Valsartan Tablets, USP due to the detection of NDEA (N-Nitrosodiethylamine) Impurity. | FDA
USA, Inc. is conducting a voluntary recall expansion of 38 lots of Valsartan and...Initiates a Voluntary Nationwide Consumer Level Recall Expansion of 38 Lots of...Impurity. When a company announces a recall, market withdrawal, or safety alert
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/aurobindopharma-usa-inc-initiates-voluntary-nationwide-consumer-level-recall-expansion-38-lots
Auromedics Pharma LLC Issues Voluntary Nationwide Recall of Ampicillin and Sulbactam For Injection USP 3 Grams Due to The Presence of Visible Particulate Matter | FDA
AuroMedics Pharma LLC is voluntarily recalling two lots of Ampicillin and Sulbactam...vial, to the hospital/user level. The recall has been initiated due to customer...Auromedics Pharma LLC Issues Voluntary Nationwide Recall of Ampicillin and Sulbactam For...Matter When a company announces a recall, market withdrawal, or safety alert
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/auromedics-pharma-llc-issues-voluntary-nationwide-recall-ampicillin-and-sulbactam-injection-usp-3
AmEx Pharmacy Issues Voluntary Nationwide Recall for one Lot of Bevacizumab 1.25mg/0.05mL 31 G Syringe Due to Reported Defective Delivery System | FDA
AmEx Pharmacy is voluntarily recalling one Lot of Bevacizumab 1.25mg/0.05mL...AmEx Pharmacy Issues Voluntary Nationwide Recall for one Lot of Bevacizumab 1...System When a company announces a recall, market withdrawal, or safety alert
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/amex-pharmacy-issues-voluntary-nationwide-recall-one-lot-bevacizumab-125mg005ml-31-g-syringe-due
AuroMedics Pharma LLC Issues Voluntary Nationwide Recall of Piperacillin and Tazobactam for Injection 3.375 grams per Vial, Due to Presence of Particulates Identified as Glass and Silicone Material | FDA
AuroMedics Pharma LLC is voluntarily recalling two lots of Piperacillin and Tazobactam...AuroMedics Pharma LLC Issues Voluntary Nationwide Recall of Piperacillin and Tazobactam...Material When a company announces a recall, market withdrawal, or safety alert
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/auromedics-pharma-llc-issues-voluntary-nationwide-recall-piperacillin-and-tazobactam-injection-3375
Prinston Pharmaceutical Inc Issues Voluntary Nationwide Recall of Valsartan and Valsartan HCTZ Tablets Due to Detection of a Trace Amount of Unexpected Impurity, N-Nitrosodimethylamine (NDMA) in The Products | FDA
Inc. dba Solco Healthcare LLC. is recalling all lots of Valsartan Tablets, 40...to the retail level. This product recall is due to the detection of a trace...Pharmaceutical Inc Issues Voluntary Nationwide Recall of Valsartan and Valsartan HCTZ...Products When a company announces a recall, market withdrawal, or safety alert
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/prinston-pharmaceutical-inc-issues-voluntary-nationwide-recall-valsartan-and-valsartan-hctz-tablets
Rugby Laboratories Issues Voluntary Nationwide Recall of Diocto Liquid and Diocto Syrup Manufactured By PharmaTech, LLC Due to Possible Product Contamination | FDA
Laboratories of Livonia, MI is voluntarily recalling all lots within the expiry of Diocto...Laboratories Issues Voluntary Nationwide Recall of Diocto Liquid and Diocto Syrup...Contamination When a company announces a recall, market withdrawal, or safety alert
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/rugby-laboratories-issues-voluntary-nationwide-recall-diocto-liquid-and-diocto-syrup-manufactured
SD Import Issues Voluntary Nationwide Recall of Aphrodisiac Capsules Due to Presence of Undeclared Sildenafil | FDA
ANNOUNCEMENT SD Import Issues Voluntary Nationwide Recall of Aphrodisiac Capsules Due to...Sildenafil When a company announces a recall, market withdrawal, or safety alert
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/sd-import-issues-voluntary-nationwide-recall-aphrodisiac-capsules-due-presence-undeclared-sildenafil
World Organix, LLC Issues Voluntary Nationwide Recall of Blissful Remedies Red Maeng Da 100% Mitragyna Speciosa, Blissful Remedies Red Maeng Da Liquid Kratom Mitragyna Speciosa, Blissful Remedies 4 Hour Chill Slow Motion Blend, Due to High Microbial Loads Contamination | FDA
World Organix LLC, is voluntarily recalling lot: 112710 of Blissful Remedies...Maeng Da 100% Mitragyna Speciosa, recalled due to Salmonella contamination, where...Organix, LLC Issues Voluntary Nationwide Recall of Blissful Remedies Red Maeng...Microbial Loads Contamination More Recalls, Market Withdrawals, & Safety Alerts
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/world-organix-llc-issues-voluntary-nationwide-recall-blissful-remedies-red-maeng-da-100-mitragyna
Liveyon, LLC Issues a Voluntary Nationwide Recall of the Regen Series ® Product, Manufactured by Genetech, Inc. | FDA
Liveyon, LLC Issues a Voluntary Nationwide Recall of the Regen Series ® Product...Genetech, Inc. When a company announces a recall, market withdrawal, or safety alert
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/liveyon-llc-issues-voluntary-nationwide-recall-regen-series-r-product-manufactured-genetech-inc
Par Pharmaceutical, Inc. Issues Voluntary Nationwide Recall of One Lot of Mycophenolate Mofetil for Injection, USP Due to the Presence of a Glass Fragment Observed in One Vial of Reconstituted Product | FDA
Pharmaceutical, Inc., is voluntarily recalling one lot of Mycophenolate Mofetil...Pharmaceutical, Inc. Issues Voluntary Nationwide Recall of One Lot of Mycophenolate Mofetil...Product When a company announces a recall, market withdrawal, or safety alert
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/par-pharmaceutical-inc-issues-voluntary-nationwide-recall-one-lot-mycophenolate-mofetil-injection
Aurobindo Pharma USA, Inc. Initiates Voluntary Nationwide Consumer Level Recall of 80 Lots of Amlodipine Valsartan Tablets USP, Valsartan HCTZ Tablets, USP and Valsartan Tablets USP, Due to the Detection of NDEA (N-Nitrosodiethylamine) Impurity | FDA
USA, Inc. is conducting a voluntary recall of 80 lots of Amlodipine Valsartan... Initiates Voluntary Nationwide Consumer Level Recall of 80 Lots of Amlodipine...Impurity 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-initiates-voluntary-nationwide-consumer-level-recall-80-lots-amlodipine
Apotex Corp. Issues Voluntary Nationwide Recall of Fluticasone Propionate Nasal Spray USP 50 mcg Per Spray 120 Metered Sprays Due to Potential for Small Glass Particles | FDA
Apotex Corp. is voluntarily recalling one (1) lot of Fluticasone Propionate...Apotex Corp. Issues Voluntary Nationwide Recall of Fluticasone Propionate Nasal...Particles 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-fluticasone-propionate-nasal-spray-usp-50-mcg-spray
Camber Pharmaceuticals, Inc. Issues Voluntary Nationwide Recall of Losartan Potassium Tablets, USP, 25 mg, 50 mg and 100 mg Due to the Detection of Trace Amounts of N-Nitroso N-Methyl 4-amino butyric acid (NMBA) Impurity found in the Active Pharmaceutical Ingredient (API) | FDA
This recall was prompted due to the detection of trace amounts of N-Nitroso...Pharmaceuticals, Inc. Issues Voluntary Nationwide Recall of Losartan Potassium Tablets...Ingredient (API) When a company announces a recall, market withdrawal, or safety alert
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/camber-pharmaceuticals-inc-issues-voluntary-nationwide-recall-losartan-potassium-tablets-usp-25-mg
Glenmark Pharmaceuticals Inc., USA Voluntarily Recalls All Unexpired Lots of its Ranitidine Tablets and Ceases Distribution, Due to Possible Presence of N-nitrosodimethylamine (NDMA) Impurity | FDA
...(“Glenmark”) today announced the voluntary recall of all unexpired lots of Ranitidine...Pharmaceuticals Inc., USA Voluntarily Recalls All Unexpired Lots of its Ranitidine...Impurity When a company announces a recall, market withdrawal, or safety alert
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/glenmark-pharmaceuticals-inc-usa-voluntarily-recalls-all-unexpired-lots-its-ranitidine-tablets-and
Almark Foods Expanded Recall to all Products from its Georgia Facility Due to Possible Listeria monocytogenes Contamination | FDA
Almark Foods is expanding its voluntary recall to include all hard-boiled eggs manufactured...ANNOUNCEMENT Almark Foods Expanded Recall to all Products from its Georgia Facility...Contamination When a company announces a recall, market withdrawal, or safety alert
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/almark-foods-expanded-recall-all-products-its-georgia-facility-due-possible-listeria-monocytogenes
Mondelēz Global LLC Conducts Voluntary Recall of Limited Quantity of Cheese Nips (11 oz. Box) Product in the U.S. Due to Potential Presence of Foreign Material | FDA
Global LLC announced today a voluntary recall of a limited quantity of Cheese Nips...Mondelēz Global LLC Conducts Voluntary Recall of Limited Quantity of Cheese Nips...Material When a company announces a recall, market withdrawal, or safety alert
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/mondelez-global-llc-conducts-voluntary-recall-limited-quantity-cheese-nips-11-oz-box-product-us-due
Bristol-Myers Squibb Voluntarily Recalls One Lot of Eliquis (apixaban) 5 mg Tablets | FDA
Company (NYSE: BMY) is voluntarily recalling one lot (#HN0063) of Eliquis 5 mg...level. This lot was distributed nationwide in the U.S. to wholesalers and retail...ANNOUNCEMENT Bristol-Myers Squibb Voluntarily Recalls One Lot of Eliquis (apixaban) 5 mg...Tablets When a company announces a recall, market withdrawal, or safety alert
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/bristol-myers-squibb-voluntarily-recalls-one-lot-eliquis-apixaban-5-mg-tablets
Apotex Corp. Issues Voluntary Nationwide Recall of Piperacillin and Tazobactam For Injection, USP 3.375 Gram/Vial And 4.5 Gram/Vial Strengths Due to Elevated Levels of Impurities That May Result in Decreased Potency | FDA
Apotex Corp. is voluntarily recalling 36 lots of Piperacillin and Tazobactam...Apotex Corp. Issues Voluntary Nationwide Recall of Piperacillin and Tazobactam...Potency 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-piperacillin-and-tazobactam-injection-usp-3375