Search Results for Nationwide recall
Showing results 921 - 940 of 975 for Nationwide recall.
Midwest Northern Nut Issues Voluntary Allergy Alert On Various Undeclared Allergens In Their Nut And Seed Snack Products | FDA
This recall has been completed and FDA has terminated this recall....Products This recall has been completed and FDA has terminated this recall. When a...a company announces a recall, market withdrawal, or safety alert, the FDA posts
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/midwest-northern-nut-issues-voluntary-allergy-alert-various-undeclared-allergens-their-nut-and-seed
STIFF BOY LLC. Issues Voluntary Nationwide Recall of THE BEAST Capsules Due to Presence of Undeclared Sildenafil | FDA
STIFF BOY LLC. is voluntarily recalling all lots within expiry of The Beast...STIFF BOY LLC. Issues Voluntary Nationwide Recall of THE BEAST 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/stiff-boy-llc-issues-voluntary-nationwide-recall-beast-capsules-due-presence-undeclared-sildenafil
Nature’s Rx Issues Voluntary Nationwide Recall of Silver Bullet 10x to Undeclared PDE-5 Inhibitors in the Product | FDA
Nature’s Rx is voluntarily recalling quantity lots of Silver Bullet 10x, description...hospital, retail or consumer level. This recall has been initiated because the product...Nature’s Rx Issues Voluntary Nationwide Recall of Silver Bullet 10x to Undeclared...Product When a company announces a recall, market withdrawal, or safety alert
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/natures-rx-issues-voluntary-nationwide-recall-silver-bullet-10x-undeclared-pde-5-inhibitors-product
Teva Pharmaceuticals USA Issues Voluntary Nationwide Recall of all Amlodipine/Valsartan Combination Tablets and Amlodipine/Valsartan/Hydrochlorothiazide Combination Tablets that are Within Expiry | FDA
Pharmaceuticals has initiated a voluntary recall in the United States, to the patient...Pharmaceuticals USA Issues Voluntary Nationwide Recall of all Amlodipine/Valsartan Combination...Expiry When a company announces a recall, market withdrawal, or safety alert
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/teva-pharmaceuticals-usa-issues-voluntary-nationwide-recall-all-amlodipinevalsartan-combination
Fresenius Kabi Issues Voluntary Nationwide Recall of Two Lots of Fluorouracil Injection Due to the Potential for Glass Particulate | FDA
Fresenius Kabi USA, LLC is voluntarily recalling two lots of Fluorouracil Injection...Fresenius Kabi Issues Voluntary Nationwide Recall of Two Lots of Fluorouracil Injection...Particulate When a company announces a recall, market withdrawal, or safety alert
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/fresenius-kabi-issues-voluntary-nationwide-recall-two-lots-fluorouracil-injection-due-potential
Updated: Torrent Pharmaceuticals Limited Expands Voluntary Nationwide Recall of Losartan Potassium Tablets, USP and Losartan Potassium/Hydrochlorothiazide Tablets, USP | FDA
Pharmaceuticals Limited is expanding its recall for Losartan Potassium Tablets USP...Pharmaceuticals Limited Expands Voluntary Nationwide Recall of Losartan Potassium Tablets...Tablets, USP When a company announces a recall, market withdrawal, or safety alert
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/updated-torrent-pharmaceuticals-limited-expands-voluntary-nationwide-recall-losartan-potassium
Camber Pharmaceuticals, Inc. Issues Voluntary Nationwide Recall of Montelukast Tablets USP, 10mg 30Ct. Due to Product/Label Mix-Up | FDA
Pharmaceuticals, Inc. is voluntarily recalling one single lot of Montelukast Sodium...10mg, to the consumer level. This recall of one batch of Montelukast Sodium...Pharmaceuticals, Inc. Issues Voluntary Nationwide Recall of Montelukast Tablets USP, 10mg...Mix-Up 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-montelukast-tablets-usp-10mg-30ct-due
Silver Star Brands, Inc. Issues Voluntary Nationwide Recall of Human and Animal Drug Products Due to Microbial Contamination | FDA
Brands, Inc., is initiating a voluntary recall of six products for humans (including...Brands, Inc. Issues Voluntary Nationwide Recall of Human and Animal Drug Products...Contamination When a company announces a recall, market withdrawal, or safety alert
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/silver-star-brands-inc-issues-voluntary-nationwide-recall-human-and-animal-drug-products-due
Auromedics Pharma LLC Issues Voluntary Nationwide Recall of Product Piperacillin and Tazobactam For Injection 3.375 Grams Per Vial, Due to Presence of Glass Particulates | FDA
AuroMedics Pharma LLC is voluntarily recalling two lots of Piperacillin and Tazobactam...Auromedics Pharma LLC Issues Voluntary Nationwide Recall of Product Piperacillin and Tazobactam...Particulates 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-product-piperacillin-and-tazobactam
UpSpring LLC Issues Allergy Alert On Undeclared Milk In "UpSpring Baby Iron + Immunity" | FDA
UpSpring LLC of Austin, TX is recalling one batch of its 60 ml dark brown glass...Immunity" When a company announces a recall, market withdrawal, or safety alert...Announcement View Product Photos More Recalls, Market Withdrawals, & Safety Alerts
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/upspring-llc-issues-allergy-alert-undeclared-milk-upspring-baby-iron-immunity
NOVIS PR LLC Issues Voluntary Nationwide Recall of PECGEN DMX Due to a Labeling Error | FDA
Novis PR LLC is voluntarily recalling 5 lots of PECGEN DMX, 16 oz, a liquid...Voluntary Nationwide Recall of PECGEN DMX Due to a Labeling Error More Recalls, Market...Over-the-Counter Drugs Reason for Announcement: Recall Reason Description Incorrect dosage
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/novis-pr-llc-issues-voluntary-nationwide-recall-pecgen-dmx-due-labeling-error
Fresenius Kabi Issues Voluntary Nationwide Recall of Sodium Chloride Injection, USP, 0.9% Due to Product Labeling Incorrectly Stating Stoppers Do Not Contain Latex | FDA
Fresenius Kabi USA is voluntarily recalling 163 lots of Sodium Chloride Injection...user level. The product is being recalled because the stoppers contain natural...Fresenius Kabi Issues Voluntary Nationwide Recall of Sodium Chloride Injection...Contain Latex When a company announces a recall, market withdrawal, or safety alert
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/fresenius-kabi-issues-voluntary-nationwide-recall-sodium-chloride-injection-usp-09-due-product
Pharm D Solutions, LLC Issues Voluntary Nationwide Recall of all Sterile Compounded Drugs Due to A Potential Lack of Sterility Assurance | FDA
Pharm D Solutions, LLC is voluntarily recalling all sterile compounded drug products...drug products are being voluntarily recalled due to concerns that practices at...Solutions, LLC Issues Voluntary Nationwide Recall of all Sterile Compounded Drugs...Assurance When a company announces a recall, market withdrawal, or safety alert
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/pharm-d-solutions-llc-issues-voluntary-nationwide-recall-all-sterile-compounded-drugs-due-potential
Legacy Pharmaceutical Packaging, LLC Expands Voluntary Nationwide Recall of Losartan Potassium Tablets, USP, 50mg 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
LLC is expanding its consumer-level recall of 3 repackaged lots Losartan Tablets...Packaging, LLC Expands 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/legacy-pharmaceutical-packaging-llc-expands-voluntary-nationwide-recall-losartan-potassium-tablets
UPDATED: Torrent Pharmaceuticals Limited Issues Voluntary Nationwide Recall of Losartan Potassium Tablets, USP and Losartan Potassium and Hydrochlorothiazide Tablets, USP | FDA
Limited is expanding its voluntary recall from 10 lots of Losartan potassium...Pharmaceuticals Limited Issues Voluntary Nationwide Recall of Losartan Potassium Tablets...Tablets, USP When a company announces a recall, market withdrawal, or safety alert
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/updated-torrent-pharmaceuticals-limited-issues-voluntary-nationwide-recall-losartan-potassium
Prinston Pharmaceutical Inc. issues Voluntary Nationwide Recall of Irbesartan and Irbesartan HCTZ Tablets Due to Detection of a Trace Amount of Unexpected Impurity, N- nitrosodiethylamine (NDEA) in the Products | FDA
Healthcare LLC., has initiated a voluntary recall of one (1) lot of Irbesartan and seven...Pharmaceutical Inc. issues Voluntary Nationwide Recall of Irbesartan and Irbesartan...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-irbesartan-and-irbesartan-hctz
King Bio Issues Voluntary Nationwide Recall of Aquaflora Candida HP9, Lymph Detox, and Baby Teething Liquids Due to Microbial Contamination | FDA
King Bio is voluntarily recalling four lots of Aquaflora Candida HP9, Lymph...ANNOUNCEMENT King Bio Issues Voluntary Nationwide Recall of Aquaflora Candida HP9, Lymph...Contamination When a company announces a recall, market withdrawal, or safety alert
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/king-bio-issues-voluntary-nationwide-recall-aquaflora-candida-hp9-lymph-detox-and-baby-teething
Nuway Distributors llc Issues Voluntary [Worldwide/Nationwide] Recall of APEXXX Due to Presence of Undeclared Sildenafil | FDA
Nuway Distributors llc is voluntarily recalling all lots of APEXXX tablets to the...Issues Voluntary [Worldwide/Nationwide] Recall of APEXXX 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/nuway-distributors-llc-issues-voluntary-worldwidenationwide-recall-apexxx-due-presence-undeclared
Sunstone Organics Issues Voluntary Nationwide Recall of Select Kratom Products Due to Potential Contamination by Salmonella | FDA
Sunstone Organics Issues Voluntary Nationwide Recall of Select Kratom Products Due...Salmonella When a company announces a recall, market withdrawal, or safety alert
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/sunstone-organics-issues-voluntary-nationwide-recall-select-kratom-products-due-potential
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