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Search Results for Nationwide recall

Showing results 21 - 40 of 975 for Nationwide recall.

Azurity Pharmaceuticals, Inc. Issues Voluntary Nationwide Recall of Zenzedi® (dextroamphetamine sulfate tablets, USP) 30 mg Due to a Mislabeled Package During Manufacturing | FDA

This recall has been completed and FDA has terminated this recall....Pharmaceuticals, Inc. Issues Voluntary Nationwide Recall of Zenzedi® (dextroamphetamine...Manufacturing This recall has been completed and FDA has terminated this recall. When a
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/azurity-pharmaceuticals-inc-issues-voluntary-nationwide-recall-zenzedir-dextroamphetamine-sulfate

Neptune Resources, LLC Issues Voluntary Nationwide Recall of Neptune’s Fix | FDA

Neptune Resources, LLC is voluntarily recalling All lots of Neptune's Fix Elixir...Voluntary Nationwide Recall of Neptune’s Fix When a company announces a recall, market...Announcement View Product Photos More Recalls, Market Withdrawals, & Safety Alerts
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/neptune-resources-llc-issues-voluntary-nationwide-recall-neptunes-fix

Tenacore LLC Issues Nationwide Recall of Tenacore’s Replacement for the Front Bezel Assembly of the CareFusion Alaris 8100 Infusion Pump Module | FDA

This recall has been completed and FDA has terminated this recall....ANNOUNCEMENT Tenacore LLC Issues Nationwide Recall of Tenacore’s Replacement for...Module This recall has been completed and FDA has terminated this recall. When a
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/tenacore-llc-issues-nationwide-recall-tenacores-replacement-front-bezel-assembly-carefusion-alaris

Sandoz Inc. Issues Voluntary Nationwide Recall of One Lot of Cefazolin for Injection Due to Product Mispackaging | FDA

...(“Sandoz”) is initiating a voluntary recall of one (1) lot of Cefazolin for Injection...Sandoz Inc. Issues Voluntary Nationwide Recall of One Lot of Cefazolin for Injection...Mispackaging 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-cefazolin-injection-due-product-mispackaging

Unichem Pharmaceuticals (USA) Inc. Issues Voluntary Nationwide Recall of Cyclobenzaprine Hydrochloride Tablets USP 10 mg, Due to Mislabeling | FDA

Pharmaceuticals (USA), Inc. is voluntarily recalling one (1) lot of Cyclobenzaprine Hydrochloride...Pharmaceuticals (USA) Inc. Issues Voluntary Nationwide Recall of Cyclobenzaprine Hydrochloride...Mislabeling When a company announces a recall, market withdrawal, or safety alert
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/unichem-pharmaceuticals-usa-inc-issues-voluntary-nationwide-recall-cyclobenzaprine-hydrochloride

Soluciones Cosméticas Issues Voluntary Nationwide Recall of Bersih Hand Sanitizer Gel Due to the Potential Presence of Undeclared Methanol (Wood Alcohol) | FDA

This recall has been completed and FDA has terminated this recall....Soluciones Cosméticas Issues Voluntary Nationwide Recall of Bersih Hand Sanitizer Gel...Alcohol) This recall has been completed and FDA has terminated this recall. When a
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/soluciones-cosmeticas-issues-voluntary-nationwide-recall-bersih-hand-sanitizer-gel-due-potential

Ultra Shop Supplement Issues Voluntary Nationwide Recall of Super Panther 7K Due to Presence of Undeclared Sildenafil and Tadalafil | FDA

This recall has been completed and FDA has terminated this recall....Shop Supplement Issues Voluntary Nationwide Recall of Super Panther 7K Due to Presence...Tadalafil This recall has been completed and FDA has terminated this recall. When a
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/ultra-shop-supplement-issues-voluntary-nationwide-recall-super-panther-7k-due-presence-undeclared

Enovachem Pharmaceuticals Issues Voluntary Nationwide Recall of Dyural-40 and Dyural-80 Convenience Kits Containing Recalled Sodium Chloride Injection, USP, 0.9% Due to Latex Hazard | FDA

... Asclemed USA Inc is voluntarily recalling 20 lots of Dyural-40 and 61 lots...user level. The products include recalled Sodium Chloride, USP, 0.9% manufactured...Pharmaceuticals Issues Voluntary Nationwide Recall of Dyural-40 and Dyural-80 Convenience...Convenience Kits Containing Recalled Sodium Chloride Injection, USP, 0.9% Due
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/enovachem-pharmaceuticals-issues-voluntary-nationwide-recall-dyural-40-and-dyural-80-convenience

Precision Dose, Inc. Issues Voluntary Nationwide Recall of Paroex Chlorhexidine Gluconate Oral Rinse USP, 0.12%, 15mL Due to Microbial Contamination | FDA

This recall has been completed and FDA has terminated this recall....Precision Dose, Inc. Issues Voluntary Nationwide Recall of Paroex Chlorhexidine Gluconate...Contamination This recall has been completed and FDA has terminated this recall. When a
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/precision-dose-inc-issues-voluntary-nationwide-recall-paroex-chlorhexidine-gluconate-oral-rinse-usp

Medtech Products Inc. Issues Nationwide Recall of Little Remedies® Honey Cough Syrup Due to Microbial Contamination | FDA

...(“Medtech” or “Company”), is voluntarily recalling five lots of Little Remedies® Honey...Medtech Products Inc. Issues Nationwide Recall of Little Remedies® Honey Cough...Contamination When a company announces a recall, market withdrawal, or safety alert
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/medtech-products-inc-issues-nationwide-recall-little-remediesr-honey-cough-syrup-due-microbial

UVT, INC. Issues Voluntary Nationwide Recall of SANIDERM ADVANCED HAND SANITIZER Due to the Potential Presence of Undeclared Methanol (Wood Alcohol) | FDA

This recall has been completed and FDA has terminated this recall....ANNOUNCEMENT UVT, INC. Issues Voluntary Nationwide Recall of SANIDERM ADVANCED HAND SANITIZER...Alcohol) This recall has been completed and FDA has terminated this recall. When a
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/uvt-inc-issues-voluntary-nationwide-recall-saniderm-advanced-hand-sanitizer-due-potential-presence

EnShiShiXiangNiShangMaoYouXianGongSi Issues Voluntary Nationwide Recall of ENDURANCE BOOST WITH HORNY GOAT WEED Capsules Due To Presence of Undeclared Propoxyphenylsildenafil and Sildenafil | FDA

EnShiShiXiangNiShangMaoYouXianGongSi is voluntarily recalling one lot of ENDURANCE BOOST WITH HORNY...uXianGongSi Issues Voluntary Nationwide Recall of ENDURANCE BOOST WITH HORNY...Sildenafil When a company announces a recall, market withdrawal, or safety alert
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/enshishixiangnishangmaoyouxiangongsi-issues-voluntary-nationwide-recall-endurance-boost-horny-goat

SCYNEXIS Issues a Voluntary Nationwide Recall of BREXAFEMME® (ibrexafungerp tablets) Due to Potential for Cross Contamination with a Non-Antibacterial ßlactam Drug Substance | FDA

Inc. is conducting a voluntary nationwide recall of 2 lots of BREXAFEMME® (ibrexafungerp...ANNOUNCEMENT SCYNEXIS Issues a Voluntary Nationwide Recall of BREXAFEMME® (ibrexafungerp...Substance When a company announces a recall, market withdrawal, or safety alert
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/scynexis-issues-voluntary-nationwide-recall-brexafemmer-ibrexafungerp-tablets-due-potential-cross

GFA Production (Xiamen) Co., Ltd. Issues Voluntary Nationwide Recall of Easy Care First Aid® Burn Cream and First Aid Kits Due to Microbial Contamination | FDA

This recall has been completed and FDA has terminated this recall....(Xiamen) Co., Ltd. Issues Voluntary Nationwide Recall of Easy Care First Aid® Burn...Contamination This recall has been completed and FDA has terminated this recall. When a
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/gfa-production-xiamen-co-ltd-issues-voluntary-nationwide-recall-easy-care-first-aidr-burn-cream-and

Universal Meditech Inc. Issues Nationwide Recall of Skippack Medical Lab SARS-CoV-2 Antigen Rapid Test Kit | FDA

Universal Meditech Inc. initiated a nationwide recall of 56,300 Skippack Medical Lab...Universal Meditech Inc. Issues Nationwide Recall of Skippack Medical Lab SARS-CoV-2...Test Kit When a company announces a recall, market withdrawal, or safety alert
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/universal-meditech-inc-issues-nationwide-recall-skippack-medical-lab-sars-cov-2-antigen-rapid-test

Novartis Issues Voluntary US Nationwide Recall of Two Lots of Sandimmune® Oral Solution (Cyclosporine Oral Solution, USP), 100 mg/mL Due to Crystallization | FDA

Novartis is conducting a voluntary nationwide recall at the consumer level of two...Novartis Issues Voluntary US Nationwide Recall of Two Lots of Sandimmune® Oral...Crystallization When a company announces a recall, market withdrawal, or safety alert
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/novartis-issues-voluntary-us-nationwide-recall-two-lots-sandimmuner-oral-solution-cyclosporine-oral

VistaPharm LLC Issues Voluntary Nationwide Recall of Sucralfate Oral Suspension, 1g/10mL Due to Microbial Contamination Identified as Bacillus Cereus | FDA

This recall has been completed and FDA has terminated this recall....VistaPharm LLC Issues Voluntary Nationwide Recall of Sucralfate Oral Suspension...Cereus This recall has been completed and FDA has terminated this recall. When a
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/vistapharm-llc-issues-voluntary-nationwide-recall-sucralfate-oral-suspension-1g10ml-due-microbial

Nostrum Laboratories, Inc. Issues Voluntary Nationwide Recall of Sucralfate Tablets USP 1 Gram Within Expiry | FDA

Nostrum Labs is initiating a voluntary recall of Sucralfa...Laboratories, Inc. Issues Voluntary Nationwide Recall of Sucralfate Tablets USP 1 Gram...Expiry When a company announces a recall, market withdrawal, or safety alert
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/nostrum-laboratories-inc-issues-voluntary-nationwide-recall-sucralfate-tablets-usp-1-gram-within

Bionpharma Inc. Issues Voluntary Nationwide Recall of Atovaquone Oral Suspension Due to Bacterial Contamination | FDA

NJ, Bionpharma Inc. is voluntarily recalling (1) single Batch (2310083) of Atovaquone...Bionpharma Inc. Issues Voluntary Nationwide Recall of Atovaquone Oral Suspension...Contamination When a company announces a recall, market withdrawal, or safety alert
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/bionpharma-inc-issues-voluntary-nationwide-recall-atovaquone-oral-suspension-due-bacterial

The Harvard Drug Group, LLC Issues Voluntary Nationwide Recall of Certain Rugby® Laboratories Brand Eye Drops Supplied by Velocity Pharma, LLC Due to Potential Risk of Eye Infections | FDA

This recall has been completed and FDA has terminated this recall....Drug Group, LLC Issues Voluntary Nationwide Recall of Certain Rugby® Laboratories...Infections This recall has been completed and FDA has terminated this recall. When a
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/harvard-drug-group-llc-issues-voluntary-nationwide-recall-certain-rugbyr-laboratories-brand-eye