Search Results for Nationwide recall
Showing results 81 - 100 of 975 for Nationwide recall.
Sun Pharmaceutical Industries, Inc. Issues Voluntary Nationwide Recall of RIOMET ER™ (Metformin Hydrochloride for Extended-Release Oral Suspension) Due to N-Nitrosodimethylamine (NDMA) Content Above the Acceptable Daily Intake (ADI) Limit | FDA
This recall has been completed and FDA has terminated this recall....Industries, Inc. Issues Voluntary Nationwide Recall of RIOMET ER™ (Metformin Hydrochloride...Limit This recall has been completed and FDA has terminated this recall. When a
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/sun-pharmaceutical-industries-inc-issues-voluntary-nationwide-recall-riomet-ertm-metformin
Grupo Yacana México S.A.S De C.V. Issues Voluntary Nationwide Recall of All Lots of Yacana Hand Sanitizer Due to Potential Presence of Methanol (Wood Alcohol) and Sub-Potent Ethanol | FDA
This recall has been completed and FDA has terminated this recall....A.S De C.V. Issues Voluntary Nationwide Recall of All Lots of Yacana Hand Sanitizer...Ethanol This recall has been completed and FDA has terminated this recall. When a
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/grupo-yacana-mexico-sas-de-cv-issues-voluntary-nationwide-recall-all-lots-yacana-hand-sanitizer-due
Lupin Pharmaceuticals, Inc. Issues Voluntary Nationwide Recall of 2 Lots of Tydemy™ (Drospirenone, Ethinyl Estradiol and Levomefolate Calcium Tablets 3mg/0.03mg/0.451mg and Levomefolate Calcium Tablets 0.451mg) Due to Out of Specification (OOS) Results at the 12-month Stability Time Point | FDA
This recall has been completed and FDA has terminated this recall....Pharmaceuticals, Inc. Issues Voluntary Nationwide Recall of 2 Lots of Tydemy™ (Drospirenone...Point This recall has been completed and FDA has terminated this recall. When a
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/lupin-pharmaceuticals-inc-issues-voluntary-nationwide-recall-2-lots-tydemytm-drospirenone-ethinyl
Med Man Expands Voluntary Nationwide Recall of Up2 and Bow & Arrow Due to Presence of Undeclared Sildenafil | FDA
This recall has been completed and FDA has terminated this recall....ANNOUNCEMENT Med Man Expands Voluntary Nationwide Recall of Up2 and Bow & Arrow Due to...Sildenafil This recall has been completed and FDA has terminated this recall. When a
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/med-man-expands-voluntary-nationwide-recall-up2-and-bow-arrow-due-presence-undeclared-sildenafil
Glenmark Pharmaceuticals Inc., USA Issues Voluntary Nationwide Recall for Potassium Chloride Extended-Release Capsules, USP (750 mg) 10 mEq K Due to Failed Dissolution | FDA
..., USA, Mahwah, NJ is voluntarily recalling 114 batches of Potassium Chloride...consumer level. The product is being recalled because of failed dissolution. Risk...Pharmaceuticals Inc., USA 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/glenmark-pharmaceuticals-inc-usa-issues-voluntary-nationwide-recall-potassium-chloride-extended
AvKARE Issues Voluntary Nationwide Recall of Sildenafil 100mg Tablets and Trazodone 100mg Tablets Due to Product Mix-Up | FDA
This recall has been completed and FDA has terminated this recall....ANNOUNCEMENT AvKARE Issues Voluntary Nationwide Recall of Sildenafil 100mg Tablets and...Mix-Up This recall has been completed and FDA has terminated this recall. When a
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/avkare-issues-voluntary-nationwide-recall-sildenafil-100mg-tablets-and-trazodone-100mg-tablets-due
Soluciones Cosméticas Issues Voluntary Nationwide Recall of Bersih Hand Sanitizer Gel Due to The Potential Presence of Undeclared Methanol (Wood Alcohol): Updated August 7, 2020 | FDA
Soluciones Cosméticas voluntary recalled all lots of Bersih Hand Sanitizer Gel...consumer level. The products are being recalled due to the potential presence of methanol...Soluciones Cosméticas Issues Voluntary Nationwide Recall of Bersih Hand Sanitizer Gel...7, 2020 When a company announces a recall, market withdrawal, or safety alert
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/soluciones-cosmeticas-issues-voluntary-nationwide-recall-bersih-hand-sanitizer-gel-due-potential-0
S&B Shopper LLC Issues Voluntary Nationwide Recall of Imperial Extreme 2000mg Due to Presence of Undeclared Sildenafil and Tadalafil | FDA
S&B Shopper LLC is voluntarily recalling all lots of Imperial Extreme 2000mg...Shopper LLC Issues Voluntary Nationwide Recall of Imperial Extreme 2000mg Due...Tadalafil When a company announces a recall, market withdrawal, or safety alert
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/sb-shopper-llc-issues-voluntary-nationwide-recall-imperial-extreme-2000mg-due-presence-undeclared
GURU INC. Issues Voluntary Nationwide Recall of Infla-650 Herbal Dietary Supplement Capsules Due to Hidden Drug Ingredients | FDA
Lilburn, GA, GURU INC. is voluntarily recalling Infla-650 Herbal Dietary Supplement...ANNOUNCEMENT GURU INC. Issues Voluntary Nationwide Recall of Infla-650 Herbal Dietary Supplement...Ingredients When a company announces a recall, market withdrawal, or safety alert
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/guru-inc-issues-voluntary-nationwide-recall-infla-650-herbal-dietary-supplement-capsules-due-hidden
Endo USA, Inc. Issues Voluntary, Nationwide Recall of Adrenalin® Chloride Solution (EPINEPHrine Nasal Solution, USP) Due to the Potential for Administration Errors | FDA
...subsidiaries, Endo USA, Inc., is voluntarily recalling all lots within expiry of Adrenalin®...Endo USA, Inc. Issues Voluntary, Nationwide Recall of Adrenalin® Chloride Solution...Errors When a company announces a recall, market withdrawal, or safety alert
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/endo-usa-inc-issues-voluntary-nationwide-recall-adrenalinr-chloride-solution-epinephrine-nasal
Church & Dwight Co., Inc. Issues Voluntary Nationwide Recall of Zicam® Cold Remedy Nasal Swabs, Zicam® Nasal AllClear Swabs, and Orajel™ Baby Teething Swabs Due to Microbial Contamination | FDA
...& Dwight Co., Inc. is voluntarily recalling all lots within expiry of Zicam®...Dwight Co., Inc. Issues Voluntary Nationwide Recall of Zicam® Cold Remedy Nasal Swabs...Contamination When a company announces a recall, market withdrawal, or safety alert
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/church-dwight-co-inc-issues-voluntary-nationwide-recall-zicamr-cold-remedy-nasal-swabs-zicamr-nasal
AAA Cosmética, S.A. de C.V. Issues Voluntary Nationwide Recall of all Lots Within Expiry of bio aaa Advance Hand Sanitizer 480 mL Due to the Potential Presence of Undeclared Methanol (Wood Alcohol) | FDA
This recall has been completed and FDA has terminated this recall....S.A. de C.V. Issues Voluntary Nationwide Recall of all Lots Within Expiry of...Alcohol) This recall has been completed and FDA has terminated this recall. When a
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/aaa-cosmetica-sa-de-cv-issues-voluntary-nationwide-recall-all-lots-within-expiry-bio-aaa-advance
Eli Lilly and Company Issues Voluntary Nationwide Recall of One Lot of GLUCAGON® Emergency Kit Due to Loss of Potency | FDA
Company (NYSE: LLY) is voluntarily recalling lot D239382D, Expiration April 2022...the consumer/user level. Lilly is recalling lot D239382D to the patient level...and Company Issues Voluntary Nationwide Recall of One Lot of GLUCAGON® Emergency...Potency When a company announces a recall, market withdrawal, or safety alert
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/eli-lilly-and-company-issues-voluntary-nationwide-recall-one-lot-glucagonr-emergency-kit-due-loss
MasterPharm, LLC. Issues Voluntary Nationwide Recall of Finasteride Plus 1.25mg Due to the Presence of an Undeclared Antihypertensive Drug | FDA
This recall has been completed and FDA has terminated this recall....MasterPharm, LLC. Issues Voluntary Nationwide Recall of Finasteride Plus 1.25mg Due...Drug This recall has been completed and FDA has terminated this recall. When a
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/masterpharm-llc-issues-voluntary-nationwide-recall-finasteride-plus-125mg-due-presence-undeclared
ICU Medical Issues Nationwide Recall of Potassium Chloride Injection, 20 mEq and Potassium Chloride Injection, 10 mEq Due to Mislabeling | FDA
ICU Medical, Inc. is voluntarily recalling one lot each of POTASSIUM CHLORIDE...ANNOUNCEMENT ICU Medical Issues Nationwide Recall of Potassium Chloride Injection...Mislabeling When a company announces a recall, market withdrawal, or safety alert
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/icu-medical-issues-nationwide-recall-potassium-chloride-injection-20-meq-and-potassium-chloride
Roque Plast S.A. de C.V. Issues Voluntary Nationwide Recall of Command Brands Gel AntiBac Instant Hand Sanitizer Lots 200371-12, 200371OH-05, 170420OH-06, 170420OH-8 Due to Potential Presence of Methanol (Wood Alcohol) | FDA
This recall has been completed and FDA has terminated this recall....S.A. de C.V. Issues Voluntary Nationwide Recall of Command Brands Gel AntiBac...Alcohol) This recall has been completed and FDA has terminated this recall. When a
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/roque-plast-sa-de-cv-issues-voluntary-nationwide-recall-command-brands-gel-antibac-instant-hand
Dr. Reddy’s Issues a Nationwide Recall of Levetiracetam in 0.75% Sodium Chloride Injection 1,000 mg/100 mL, in the U.S., Due to Mislabeling of Infusion Bag | FDA
Dr. Reddy’s Laboratories Ltd is recalling one Batch/Lot No: A1540076 of Levetiracetam...ANNOUNCEMENT Dr. Reddy’s Issues a Nationwide Recall of Levetiracetam in 0.75% Sodium...Infusion Bag When a company announces a recall, market withdrawal, or safety alert
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/dr-reddys-issues-nationwide-recall-levetiracetam-075-sodium-chloride-injection-1000-mg100-ml-us-due
Teva Pharmaceuticals USA, Inc. Expands Voluntary Nationwide Recall of Losartan Potassium to 50 mg and 100 mg Tablets USP, Sold Exclusively to Golden State Medical Supply, Inc. | FDA
This recall has been completed and FDA has terminated this recall....Pharmaceuticals USA, Inc. Expands Voluntary Nationwide Recall of Losartan Potassium to 50 mg...Inc. This recall has been completed and FDA has terminated this recall. When a
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/teva-pharmaceuticals-usa-inc-expands-voluntary-nationwide-recall-losartan-potassium-50-mg-and-100-mg
Health Fixer Issues Voluntary Nationwide Recall of Male Ultra, Malextra, Electro Buzz, Ultra Armor and Male Ultra Pro Due to Undeclared Chloropretadalafil, Propoxyphenylsildenafil and Sildenafil | FDA
... AZ, HEALTH FIXER is voluntarily recalling all lots of dietary supplements by...Health Fixer Issues Voluntary Nationwide Recall of Male Ultra, Malextra, Electro...Sildenafil When a company announces a recall, market withdrawal, or safety alert
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/health-fixer-issues-voluntary-nationwide-recall-male-ultra-malextra-electro-buzz-ultra-armor-and
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