Search Results for Nationwide recall
Showing results 221 - 240 of 975 for Nationwide recall.
Recall Reminder: Gerber Products Company Previously Recalled and Discontinued All Batches of Gerber® Soothe N Chew® Teething Sticks Due To Potential Choking Hazard | FDA
Gerber Products Company initiated a recall and discontinuation of all batches...ANNOUNCEMENT Recall Reminder: Gerber Products Company Previously Recalled and Discontinued...Hazard When a company announces a recall, market withdrawal, or safety alert
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/recall-reminder-gerber-products-company-previously-recalled-and-discontinued-all-batches-gerberr
The Salsa Texan Issues Allergy Alert and Recall Expansion for Undeclared Wheat and Milk in Tortillas | FDA
This recall has been completed and FDA has terminated this recall....Salsa Texan Issues Allergy Alert and Recall Expansion for Undeclared Wheat and...Tortillas This recall has been completed and FDA has terminated this recall. When a
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/salsa-texan-issues-allergy-alert-and-recall-expansion-undeclared-wheat-and-milk-tortillas
Efficient Laboratories, Inc. Expands Voluntary Nationwide Recall to Consumers to Include Twelve Additional Lots of Rompe Pecho CF, Rompe Pecho EX, Rompe Pecho MAX, and Rompe Pecho DM Sold in 2019 Due to Microbial Contamination Concerns | FDA
This recall has been completed and FDA has terminated this recall....Laboratories, Inc. Expands Voluntary Nationwide Recall to Consumers to Include Twelve...Concerns This recall has been completed and FDA has terminated this recall. When a
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/efficient-laboratories-inc-expands-voluntary-nationwide-recall-consumers-include-twelve-additional
Coppertone® Issues Voluntary Nationwide Recall of Specific Lots of Pure & Simple SPF 50 Spray (2021 Launch), Sport Mineral SPF 50 Spray (2021 Launch), and Travel-Size Coppertone® Sport Spray SPF 50 (1.6OZ) Aerosols Sunscreen Sprays Due to the Presence of Benzene | FDA
This recall has been completed and FDA has terminated this recall....Coppertone® Issues Voluntary Nationwide Recall of Specific Lots of Pure & Simple...Benzene This recall has been completed and FDA has terminated this recall. When a
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/coppertoner-issues-voluntary-nationwide-recall-specific-lots-pure-simple-spf-50-spray-2021-launch
SterRx, LLC Issues Voluntary Nationwide Recall of Certain SterRx Products | FDA
...today announced the voluntary nationwide recall of approximately 240 lots within...SterRx, LLC Issues Voluntary Nationwide Recall of Certain SterRx Products When...When a company announces a recall, market withdrawal, or safety alert, the FDA
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/sterrx-llc-issues-voluntary-nationwide-recall-certain-sterrx-products
Gilead Issues A Voluntary Nationwide Recall of Two Lots of Veklury® (Remdesivir) Due to Presence of Glass Particulates | FDA
This recall has been completed and FDA has terminated this recall....ANNOUNCEMENT Gilead Issues A Voluntary Nationwide Recall of Two Lots of Veklury® (Remdesivir)...Particulates This recall has been completed and FDA has terminated this recall. When a
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/gilead-issues-voluntary-nationwide-recall-two-lots-vekluryr-remdesivir-due-presence-glass
Ascend Laboratories LLC. Issues Voluntary Nationwide Recall of Dabigatran Etexilate Capsules, USP 75 mg and 150 mg, Due to the Detection of N-Nitroso-dabigatran (NDAB) Impurity | FDA
Laboratories LLC. is voluntarily recalling Dabigatran Etcxilate Capsules. USP...Laboratories LLC. Issues Voluntary Nationwide Recall of Dabigatran Etexilate Capsules...Impurity When a company announces a recall, market withdrawal, or safety alert
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/ascend-laboratories-llc-issues-voluntary-nationwide-recall-dabigatran-etexilate-capsules-usp-75-mg
Church & Dwight Issues Voluntary Nationwide Recall of One Specific Lot of TheraBreath Strawberry Splash for Kids 16oz Sold Exclusively on Amazon Between May 31 and September 02, 2023, Due to Microbial Contamination Identified as Yeast (Candida Parapsilosis) | FDA
...(NYSE:CHD) today initiated a voluntary recall of one specific lot of TheraBreath...Church & Dwight Issues Voluntary Nationwide Recall of One Specific Lot of TheraBreath...Parapsilosis) When a company announces a recall, market withdrawal, or safety alert
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/church-dwight-issues-voluntary-nationwide-recall-one-specific-lot-therabreath-strawberry-splash-kids
Nurse Assist, LLC Issues Recall of 0.9% Sodium Chloride Irrigation USP and Sterile Water for Irrigation USP Nationwide and to Canada | FDA
Assist, LLC initiated a voluntary recall of 0.9% sodium chloride irrigation...ANNOUNCEMENT Nurse Assist, LLC Issues Recall of 0.9% Sodium Chloride Irrigation...Irrigation USP Nationwide and to Canada When a company announces a recall, market withdrawal
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/nurse-assist-llc-issues-recall-09-sodium-chloride-irrigation-usp-and-sterile-water-irrigation-usp
Male Enhancement Supplements Recalled | FDA
Products , St Louis MO is voluntarily recalling tainted lot (HGW221116) within expiry...Enhancement Supplements Recalled When a company announces a recall, market withdrawal...the company. Read Announcement More Recalls, Market Withdrawals, & Safety Alerts
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/male-enhancement-supplements-recalled
Amneal Pharmaceuticals Issues Voluntary Nationwide Recall of Lorazepam Oral Concentrate, USP 2mg/mL, Due to Misprinted Dosing Droppers Supplied with the Product | FDA
This recall has been completed and FDA has terminated this recall....Pharmaceuticals Issues Voluntary Nationwide Recall of Lorazepam Oral Concentrate...Product 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-issues-voluntary-nationwide-recall-lorazepam-oral-concentrate-usp-2mgml-due
URGENT: Nationwide Voluntary Recall of Natierra Organic Freeze- Dried Blueberry (lot # 2021363-1 & 2022026-1) Due to levels of Lead | FDA
This recall has been completed and FDA has terminated this recall....COMPANY ANNOUNCEMENT URGENT: Nationwide Voluntary Recall of Natierra Organic Freeze-...Lead This recall has been completed and FDA has terminated this recall. When a
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/urgent-nationwide-voluntary-recall-natierra-organic-freeze-dried-blueberry-lot-2021363-1-2022026-1
Tony's Chocolonely Recalls Two Chocolate Products Because They May Contain Small Stones | FDA
York Corporation, is voluntarily recalling seven lots of Tony’s brand Dark Almond...COMPANY ANNOUNCEMENT Tony's Chocolonely Recalls Two Chocolate Products Because They...Stones When a company announces a recall, market withdrawal, or safety alert
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/tonys-chocolonely-recalls-two-chocolate-products-because-they-may-contain-small-stones
Recall of La Fiesta Brand Bread Crumbs (Unseasoned and Seasoned) for Undeclared Sesame | FDA
Food Products, LLC, La Mirada, CA is recalling 8 oz packages of La Fiesta brand...COMPANY ANNOUNCEMENT Recall of La Fiesta Brand Bread Crumbs (Unseasoned and...Sesame When a company announces a recall, market withdrawal, or safety alert
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/recall-la-fiesta-brand-bread-crumbs-unseasoned-and-seasoned-undeclared-sesame
Precision Dose Inc. Issues Voluntary Nationwide Recall of Ranitidine Oral Solution, USP 150 mg/10 mL Due to Possible Presence of N-nitrosodimethylamine (NDMA) Impurity | FDA
This recall has been completed and FDA has terminated this recall....Precision Dose Inc. Issues Voluntary Nationwide Recall of Ranitidine Oral Solution,...Impurity 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-ranitidine-oral-solution-usp-150-mg10-ml-due
RXQ Compounding, LLC Issues Voluntary Nationwide Recall of All Sterile Products within Expiry and Voluntarily Cessation of Production Due to the Lack of Sterility Process Assurance | FDA
This recall has been completed and FDA has terminated this recall....Compounding, LLC Issues Voluntary Nationwide Recall of All Sterile Products within...Assurance This recall has been completed and FDA has terminated this recall. When a
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/rxq-compounding-llc-issues-voluntary-nationwide-recall-all-sterile-products-within-expiry-and
Viva Raw Issues Voluntary Recall of Two Lots of Dog an Cat Foods Due to Salmonella and Listeria Monocytogenes Contamination | FDA
LLC, Charlotte, NC is voluntarily recalling two lots of dog and cat foods due...Salmonella and Listeria monocytogenes. The recall is for Lot 21495 (Viva Ground Beef...ANNOUNCEMENT Viva Raw Issues Voluntary Recall of Two Lots of Dog an Cat Foods Due...Contamination When a company announces a recall, market withdrawal, or safety alert
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/viva-raw-issues-voluntary-recall-two-lots-dog-cat-foods-due-salmonella-and-listeria-monocytogenes
Viva Raw Issues Voluntary Recall of Two Lots of Dog and Cat Foods Due to Salmonella and Listeria Monocytogenes Contamination | FDA
LLC, Charlotte, NC is voluntarily recalling two lots of dog and cat foods due...Salmonella and Listeria monocytogenes. The recall is for Lot 21495 (Viva Ground Beef...ANNOUNCEMENT Viva Raw Issues Voluntary Recall of Two Lots of Dog and Cat Foods Due...Contamination When a company announces a recall, market withdrawal, or safety alert
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/viva-raw-issues-voluntary-recall-two-lots-dog-and-cat-foods-due-salmonella-and-listeria
Harvest NYC Inc Recalls Enoki Mushroom Due to Possible Health Risk | FDA
NYC Inc of Brooklyn, NY 11231 is recalling its 200g packages of Enoki Mushroom...COMPANY ANNOUNCEMENT Harvest NYC Inc Recalls Enoki Mushroom Due to Possible Health...Health Risk When a company announces a recall, market withdrawal, or safety alert
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/harvest-nyc-inc-recalls-enoki-mushroom-due-possible-health-risk
Chetak LLC Group Recalls Product Because of Possible Health Risk | FDA
Are recalling Frozen ‘Deep Sprouted Mat(Moth) 16 oz. and Deep Sprouted Moong...COMPANY ANNOUNCEMENT Chetak LLC Group Recalls Product Because of Possible Health...Health Risk When a company announces a recall, market withdrawal, or safety alert
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/chetak-llc-group-recalls-product-because-possible-health-risk