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Search Results for Nationwide recall

Showing results 61 - 80 of 975 for Nationwide recall.

Maquiladora Miniara S.A. de C.V. Issues Voluntary Nationwide Recall of Shine and Clean Hand Sanitizer and Due to 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 Shine and Clean 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/maquiladora-miniara-sa-de-cv-issues-voluntary-nationwide-recall-shine-and-clean-hand-sanitizer-and

Kiriko, LLC. Issues Voluntary Nationwide Recall of A1 Slim Due to Undeclared Sibutramine, Phenolphthalein and N-Desmethyl Sibutramine | FDA

..., Kiriko, LLC. is voluntarily recalling all lots of A1 Slim 30 capsules bottle...Kiriko, LLC. Issues Voluntary Nationwide Recall of A1 Slim Due to Undeclared...Sibutramine When a company announces a recall, market withdrawal, or safety alert
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/kiriko-llc-issues-voluntary-nationwide-recall-a1-slim-due-undeclared-sibutramine-phenolphthalein-and

Amneal Pharmaceutical LLC Issues a Nationwide Recall of Ropivacaine Hydrochloride Injection, USP 500mg/100mL, Due to the Potential Presence of Particulate Matter | FDA

NJ, Amneal Pharmaceutical LLC, is recalling two lots of Ropivacaine Hydrochloride...Amneal Pharmaceutical LLC Issues a Nationwide Recall of Ropivacaine Hydrochloride...Matter When a company announces a recall, market withdrawal, or safety alert
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/amneal-pharmaceutical-llc-issues-nationwide-recall-ropivacaine-hydrochloride-injection-usp

Novartis Issues Voluntary Nationwide Recall of One Lot 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 one...ANNOUNCEMENT Novartis Issues Voluntary Nationwide Recall of One Lot 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-nationwide-recall-one-lot-sandimmuner-oral-solution-cyclosporine-oral

4e Brands North America Issues Expanded Nationwide Voluntary Recall of Hand Sanitizer Due to Potential Presence of Undeclared Methanol (Wood Alcohol) | FDA

Brands North America is voluntarily recalling all lots of Hand Sanitizer brands...consumer level. These products are being recalled due to the potential presence of methanol...America Issues Expanded Nationwide Voluntary Recall of Hand Sanitizer Due to...Alcohol) When a company announces a recall, market withdrawal, or safety alert
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/4e-brands-north-america-issues-expanded-nationwide-voluntary-recall-hand-sanitizer-due-potential

Amneal Pharmaceuticals, LLC. Issues a Nationwide Voluntary Recall of Vancomycin Hydrochloride for Oral Solution USP, 250mg/5mL, Due to the Potential for Some Bottles to be Super Potent Which May be Harmful | FDA

This recall has been completed and FDA has terminated this recall....Pharmaceuticals, LLC. Issues a Nationwide Voluntary Recall of Vancomycin Hydrochloride...Harmful This recall has been completed and FDA has terminated this recall. When a
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/amneal-pharmaceuticals-llc-issues-nationwide-voluntary-recall-vancomycin-hydrochloride-oral-solution

Albek de Mexico S.A. de C.V. Issues Voluntary Nationwide Recall of All Hand Sanitizers Due to Potential Presence of Undeclared Methanol | FDA

Mexico S.A. de C.V. is voluntarily recalling all lots and all brands of hand sanitizer...November 7, 2019 and June 28, 2020. This recall is being initiated out of...S.A. de C.V. Issues Voluntary Nationwide Recall of All Hand Sanitizers Due to...Methanol When a company announces a recall, market withdrawal, or safety alert
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/albek-de-mexico-sa-de-cv-issues-voluntary-nationwide-recall-all-hand-sanitizers-due-potential

Marlex Pharmaceuticals, Inc. Issues Voluntary Nationwide Recall of Digoxin Tablets USP, 0.125mg and Digoxin Tablets USP, 0.25mg Due to Label Mix-Up | FDA

This recall has been completed and FDA has terminated this recall....Pharmaceuticals, Inc. Issues Voluntary Nationwide Recall of Digoxin Tablets USP, 0.125mg...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/marlex-pharmaceuticals-inc-issues-voluntary-nationwide-recall-digoxin-tablets-usp-0125mg-and-digoxin

One Source Nutrition, Inc. Issues Voluntary Nationwide Recall of Vitality Capsules Due to Presence of Undeclared Sildenafil and Tadalafil | FDA

One Source Nutrition is voluntarily recalling all lots of Vitality capsules to...Nutrition, Inc. Issues Voluntary Nationwide Recall of Vitality Capsules Due to Presence...Tadalafil When a company announces a recall, market withdrawal, or safety alert
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/one-source-nutrition-inc-issues-voluntary-nationwide-recall-vitality-capsules-due-presence-0

4e Brands North America Issues Nationwide Voluntary Recall of Hand Sanitizer Due to Potential Presence of Undeclared Methanol (Wood Alcohol) | FDA

Brands North America is voluntarily recalling ten (10) bottle sizes of Hand Sanitizers...consumer level. The products are being recalled due to the potential presence of methanol...Brands North America Issues Nationwide Voluntary Recall of Hand Sanitizer Due to...Alcohol) When a company announces a recall, market withdrawal, or safety alert
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/4e-brands-north-america-issues-nationwide-voluntary-recall-hand-sanitizer-due-potential-presence

Shoppers-Plaza Issues Voluntary Nationwide Recall of Fouzee Sugarlin Herbal Formula Due To Presence Of Undeclared Metformin And Glyburide | FDA

California - Shoppers-Plaza is voluntarily recalling all lots of Fouzee Sugarlin Herbal...Shoppers-Plaza Issues Voluntary Nationwide Recall of Fouzee Sugarlin Herbal Formula...Glyburide When a company announces a recall, market withdrawal, or safety alert
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/shoppers-plaza-issues-voluntary-nationwide-recall-fouzee-sugarlin-herbal-formula-due-presence

Padagis Issues Voluntary Nationwide Recall for Nitroglycerin Lingual Spray Due to a Possible Defective Delivery System | FDA

This recall has been completed and FDA has terminated this recall....ANNOUNCEMENT Padagis Issues Voluntary Nationwide Recall for Nitroglycerin Lingual Spray...System This recall has been completed and FDA has terminated this recall. When a
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/padagis-issues-voluntary-nationwide-recall-nitroglycerin-lingual-spray-due-possible-defective

Real Clean Distribuciones SA de CV Issues Voluntary Nationwide Recall of Four Hand Sanitizer Due to Potential Presence of Undeclared Methanol (Wood Alcohol) | FDA

This recall has been completed and FDA has terminated this recall....Distribuciones SA de CV Issues Voluntary Nationwide Recall of Four Hand Sanitizer Due to...Alcohol) This recall has been completed and FDA has terminated this recall. When a
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/real-clean-distribuciones-sa-de-cv-issues-voluntary-nationwide-recall-four-hand-sanitizer-due

Provepharm Inc. Issues Voluntary Nationwide Recall of One Lot of Phenylephrine Hydrochloride Injection, USP, 10 mg/ mL (Pharmacy Bulk Package) Due to Presence of Particulate Matter | FDA

Pennsylvania, Provepharm Inc. is voluntarily recalling lot number 24020027; Expiry Date...hospital/institutional level. This recall was initiated based on a customer complaint...Provepharm Inc. Issues Voluntary Nationwide Recall of One Lot of Phenylephrine Hydrochloride...Matter When a company announces a recall, market withdrawal, or safety alert
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/provepharm-inc-issues-voluntary-nationwide-recall-one-lot-phenylephrine-hydrochloride-injection-usp

VitalityVita Issues Voluntary Nationwide Recall of VitalityXtra and PeakMax Capsules Due to the Presence of Undeclared Sildenafil and Diclofenac | FDA

... VitalityVita.com is voluntarily recalling lot 230811, Exp 8/11/25, of VitalityXtra...VitalityVita Issues Voluntary Nationwide Recall of VitalityXtra and PeakMax Capsules...Diclofenac When a company announces a recall, market withdrawal, or safety alert
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/vitalityvita-issues-voluntary-nationwide-recall-vitalityxtra-and-peakmax-capsules-due-presence

The Harvard Drug Group, LLC Issues Voluntary Nationwide Recall of Dronabinol Capsules, USP, 2.5 mg and Ziprasidone Hydrochloride Capsules, 20 mg Due to Label Mix-up | FDA

This recall has been completed and FDA has terminated this recall....Drug Group, LLC Issues Voluntary Nationwide Recall of Dronabinol Capsules, USP,...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/harvard-drug-group-llc-issues-voluntary-nationwide-recall-dronabinol-capsules-usp-25-mg-and

Hospira, Inc. Issues a Voluntary Nationwide Recall for 4.2% Sodium Bicarbonate Injection, USP and 1% and 2% Lidocaine HCl Injection, USP Due to the Potential for Presence of Glass Particulate Matter | FDA

This recall has been completed and FDA has terminated this recall....Hospira, Inc. Issues a Voluntary Nationwide Recall for 4.2% Sodium Bicarbonate Injection...Matter This recall has been completed and FDA has terminated this recall. When a
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/hospira-inc-issues-voluntary-nationwide-recall-42-sodium-bicarbonate-injection-usp-and-1-and-2

Ultra Supplement LLC Issues Voluntary Nationwide Recall of Sustango Due to the Presence of Undeclared Tadalafil | FDA

This recall has been completed and FDA has terminated this recall....Supplement LLC Issues Voluntary Nationwide Recall of Sustango Due to the 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-supplement-llc-issues-voluntary-nationwide-recall-sustango-due-presence-undeclared-tadalafil

Harmonic Nature Issues Voluntary Nationwide Recall of Hand Sanitizer Due to the Presence of 1-Propanol | FDA

Leon, Harmonic Nature is voluntarily recalling all 800 bottles Hand Sanitizer, 250mL...Harmonic Nature Issues Voluntary Nationwide Recall of Hand Sanitizer Due to the...1-Propanol When a company announces a recall, market withdrawal, or safety alert
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/harmonic-nature-issues-voluntary-nationwide-recall-hand-sanitizer-due-presence-1-propanol

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