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Search Results for Nationwide recall

Showing results 141 - 160 of 975 for Nationwide recall.

C&A Naturistics Issues Voluntary Nationwide Recall of AK Forte Tablets con Ortiga y Omega 3 Due to the Presence of Undeclared Drug Ingredients: Diclofenac, Dexamethasone, and Methocarbamol | FDA

CA, C&A Naturistics is voluntarily recalling all lots of AK Forte, 400 mg tablets...Naturistics Issues Voluntary Nationwide Recall of AK Forte Tablets con Ortiga...Methocarbamol When a company announces a recall, market withdrawal, or safety alert
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/ca-naturistics-issues-voluntary-nationwide-recall-ak-forte-tablets-con-ortiga-y-omega-3-due-presence

Alcon Laboratories Issues Voluntary Nationwide Recall of One (1) Lot of Systane Lubricant Eye Drops Ultra PF, Single Vials On-the-Go, 25 count (Lot 10101), Due to Fungal Contamination | FDA

Alcon Laboratories is voluntarily recalling one (1) lot of Systane Lubricant...Laboratories Issues Voluntary Nationwide Recall of One (1) Lot of Systane Lubricant...Contamination When a company announces a recall, market withdrawal, or safety alert
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/alcon-laboratories-issues-voluntary-nationwide-recall-one-1-lot-systane-lubricant-eye-drops-ultra-pf

SoloVital.com Issues Voluntary Nationwide Recall of Umary Acido Hialuronica, Suplemento Alimenticio 850 mg Capsules Due to the Presence of Undeclared Drug Ingredients: Diclofenac and Omeprazole | FDA

CA, SoloVital.com is voluntarily recalling all lots of Umary Acido Hialuronica...SoloVital.com Issues Voluntary Nationwide Recall of Umary Acido Hialuronica, Suplemento...Omeprazole When a company announces a recall, market withdrawal, or safety alert
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/solovitalcom-issues-voluntary-nationwide-recall-umary-acido-hialuronica-suplemento-alimenticio-850

Fresenius Kabi Issues Voluntary Nationwide Recall of Ketorolac Tromethamine Injection, USP Due to the Presence of Particulate Matter | FDA

This recall has been completed and FDA has terminated this recall....Fresenius Kabi Issues Voluntary Nationwide Recall of Ketorolac Tromethamine 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/fresenius-kabi-issues-voluntary-nationwide-recall-ketorolac-tromethamine-injection-usp-due-presence

Teva Pharmaceuticals USA, Inc. Initiates Voluntary Nationwide Recall of Metformin Hydrochloride Extended-Release Tablets USP 500 mg and 750 mg Due to Detection of N-Nitrosodimethylamine (NDMA) | FDA

Pharmaceuticals USA, Inc. is voluntarily recalling fourteen (14) lots of Metformin Hydrochloride...USA, Inc. Initiates Voluntary Nationwide Recall of Metformin Hydrochloride Extended-Release...(NDMA) When a company announces a recall, market withdrawal, or safety alert
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/teva-pharmaceuticals-usa-inc-initiates-voluntary-nationwide-recall-metformin-hydrochloride-extended

Insight Pharmaceuticals Issues Voluntary Nationwide Recall of TING® 1% Tolnaftate Athlete’s Foot Spray Antifungal Spray Liquid Due to the Presence of Benzene | FDA

...company (“Insight”), is voluntarily recalling two lots of TING® 1% Tolnaftate Athlete’s...Pharmaceuticals Issues Voluntary Nationwide Recall of TING® 1% Tolnaftate Athlete’s...Benzene When a company announces a recall, market withdrawal, or safety alert
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/insight-pharmaceuticals-issues-voluntary-nationwide-recall-tingr-1-tolnaftate-athletes-foot-spray

Botanical-Be Issues Voluntary Nationwide Recall of Kuka Flex Forte, Reumo Flex (Caplets) and Artri King (Tablets). Due to Presence of Undeclared Diclofenac | FDA

Botanical-Be has voluntarily initiated a recall of all batches of Kuka Flex Forte caplets...caplets, and Artri King tablets. This recall is directed at the consumer...Botanical-Be Issues Voluntary Nationwide Recall of Kuka Flex Forte, Reumo Flex...Diclofenac When a company announces a recall, market withdrawal, or safety alert
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/botanical-be-issues-voluntary-nationwide-recall-kuka-flex-forte-reumo-flex-caplets-and-artri-king

Endo USA, Inc. Issues Voluntary, Nationwide Recall of One Lot of Clonazepam Orally Disintegrating Tablets, USP (C-IV) Lot Number 550147301 Due to Mislabeling: Incorrect Strength on Product Carton | FDA

...subsidiaries, Endo USA, Inc., is voluntarily recalling one lot of Clonazepam Orally Disintegrating...Endo USA, Inc. Issues Voluntary, Nationwide Recall of One Lot of Clonazepam Orally...Carton 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-one-lot-clonazepam-orally-disintegrating-tablets-usp

Noah’s Wholesale, LLC Issues Voluntary Nationwide Recall of the Rock Due to Presence of Undeclared Sildenafil | FDA

Noah’s Wholesale, LLC is voluntarily recalling one lot of the rock# 03032021,exp:12/2027...Wholesale, LLC Issues Voluntary Nationwide Recall of the Rock Due to Presence of...Sildenafil When a company announces a recall, market withdrawal, or safety alert
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/noahs-wholesale-llc-issues-voluntary-nationwide-recall-rock-due-presence-undeclared-sildenafil

WS Global Issues Nationwide Recall of Himalayan Pain Relief Tea Due to the Presence of Hidden Drug Ingredients, Diclofenac and Dexamethasone | FDA

... INC Brooklyn, NY is voluntarily recalling all lots of Himalayan Pain Relief...ANNOUNCEMENT WS Global Issues Nationwide Recall of Himalayan Pain Relief Tea...Dexamethasone When a company announces a recall, market withdrawal, or safety alert
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/ws-global-issues-nationwide-recall-himalayan-pain-relief-tea-due-presence-hidden-drug-ingredients

Hikma Pharmaceuticals USA Inc. Extends Voluntary Nationwide Recall of One Lot of Acetaminophen Injection, 1000mg/100mL, (10mg/mL) Bags Due to an Individual Unit of Acetaminophen Overwrap Found to Have Contained a Labelled Bag of Dexmedetomidine HCL Injection (400mcg/100mL) | FDA

USA, Inc. is extending its voluntary recall of one lot (listed below) of Acetaminophen...consumer/user level. The product is being recal...Pharmaceuticals USA Inc. Extends Voluntary Nationwide Recall of One Lot of Acetaminophen Injection...(400mcg/100mL) When a company announces a recall, market withdrawal, or safety alert
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/hikma-pharmaceuticals-usa-inc-extends-voluntary-nationwide-recall-one-lot-acetaminophen-injection

YoCrunch® Products Voluntarily Recalled by Danone U.S. Due to Potential Presence of Plastic Pieces in Dome Topper | FDA

...voluntarily recalling YoCrunch® products sold at retail stores nationwide due to...ANNOUNCEMENT YoCrunch® Products Voluntarily Recalled by Danone U.S. Due to Potential Presence...Topper When a company announces a recall, market withdrawal, or safety alert
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/yocrunchr-products-voluntarily-recalled-danone-us-due-potential-presence-plastic-pieces-dome-topper

Meta Herbal Issues Voluntary Nationwide Recall of Magnum XXL 9800 Capsules Due to Presence of Undeclared Sildenafil | FDA

Hampton NY- Meta Herbal is voluntarily recalling 500 blister packs of Magnum XXL 9800...Meta Herbal Issues Voluntary Nationwide Recall of Magnum XXL 9800 Capsules Due...Sildenafil When a company announces a recall, market withdrawal, or safety alert
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/meta-herbal-issues-voluntary-nationwide-recall-magnum-xxl-9800-capsules-due-presence-undeclared

SugarMDs LLC Issues Voluntary Nationwide Recall of Advanced Glucose Support Supplements Capsules Due to Presence of Undeclared Glyburide and Metformin | FDA

MO, SugarMDs, LLC is voluntarily recalling Lot: 22165-003 Advance Glucose Support...SugarMDs LLC Issues Voluntary Nationwide Recall of Advanced Glucose Support Supplements...Metformin When a company announces a recall, market withdrawal, or safety alert
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/sugarmds-llc-issues-voluntary-nationwide-recall-advanced-glucose-support-supplements-capsules-due

Adamis Pharmaceuticals Corporation Issues Nationwide Voluntary Recall of SYMJEPI® (Epinephrine) Injection for Potential Manufacturing Defect | FDA

This recall has been completed and FDA has terminated this recall....Pharmaceuticals Corporation Issues Nationwide Voluntary Recall of SYMJEPI® (Epinephrine)...Defect This recall has been completed and FDA has terminated this recall. When a
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/adamis-pharmaceuticals-corporation-issues-nationwide-voluntary-recall-symjepir-epinephrine-injection

Miracle8989 Issues Voluntary Nationwide Recall of PremierZen Gold 7000, PremierZen Platinum 8000 and MaxxZEN Platinum 12000, Due to Presence of Undeclared Sildenafil and Tadalafil | FDA

This recall has been completed and FDA has terminated this recall....Miracle8989 Issues Voluntary Nationwide Recall of PremierZen Gold 7000, PremierZen...Tadalafil This recall has been completed and FDA has terminated this recall. When a
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/miracle8989-issues-voluntary-nationwide-recall-premierzen-gold-7000-premierzen-platinum-8000-and

Teva Issues Voluntary Nationwide Recall of One Lot of IDArubicin Hydrochloride Injection USP 5 mg/5 mL Due to the Presence of Particulate Matter | FDA

This recall has been completed and FDA has terminated this recall....ANNOUNCEMENT Teva Issues Voluntary Nationwide Recall of One Lot of IDArubicin Hydrochloride...Matter This recall has been completed and FDA has terminated this recall. When a
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/teva-issues-voluntary-nationwide-recall-one-lot-idarubicin-hydrochloride-injection-usp-5-mg5-ml-due

Haleon Issues Voluntary Nationwide Recall of Robitussin Honey CF Max Day Adult and Robitussin Honey CF Max Nighttime Adult Products Due to Microbial Contamination | FDA

Haleon is voluntarily recalling eight lots of Robitussin Honey CF Max Day Adult...consumer level. The product is being recalled due to microbial contamination. In...ANNOUNCEMENT Haleon Issues Voluntary Nationwide Recall of Robitussin Honey CF Max Day...Contamination When a company announces a recall, market withdrawal, or safety alert
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/haleon-issues-voluntary-nationwide-recall-robitussin-honey-cf-max-day-adult-and-robitussin-honey-cf

PNHC, LLC d/b/a Heal the World Issues Voluntary Nationwide Recall of Heal the World Hand Sanitizer Packaged in 9.6 Ounce Bottles Because They Resemble Small Water Bottles | FDA

This recall has been completed and FDA has terminated this recall....Heal the World Issues Voluntary Nationwide Recall of Heal the World Hand Sanitizer...Bottles This recall has been completed and FDA has terminated this recall. When a
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/pnhc-llc-dba-heal-world-issues-voluntary-nationwide-recall-heal-world-hand-sanitizer-packaged-96

Brassica Pharma Pvt. Ltd. Issues Voluntary Nationwide Recall of Equate Lubricant Eye Ointment, Equate Stye Lubricant Eye Ointment, CVS Health Lubricant Eye Ointment, Lubricant PM Ointment Due to Potential Lack of Sterility | FDA

Brassica Pharma Pvt. Ltd. is voluntarily recalling Eye Ointment products listed in the...September 2025. The products are being recalled due to lack of sterility assurance...Pharma Pvt. Ltd. Issues Voluntary Nationwide Recall of Equate Lubricant Eye Ointment...Sterility When a company announces a recall, market withdrawal, or safety alert
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/brassica-pharma-pvt-ltd-issues-voluntary-nationwide-recall-equate-lubricant-eye-ointment-equate-stye