Search Results for FOOD DIRECTIONS
Showing results 41 - 60 of 104 for FOOD DIRECTIONS.
Baloian Farms of Arizona Co., Recalls Whole Fresh American Cucumbers Because of Possible Health Risks Due to Salmonella | FDA
November 15, 2024. Discussions with the US Food and Drug Administration (“FDA”) confirmed...this. Baloian is also contacting its direct buyers to advise them of the recall
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/baloian-farms-arizona-co-recalls-whole-fresh-american-cucumbers-because-possible-health-risks-due
Sandoz Inc. Issues Voluntary Recall of Ranitidine Hydrochloride Capsules 150mg and 300mg Due to An Elevated Amount of Unexpected Impurity, N-Nitrosodimethylamine (NDMA), in the Product | FDA
...contaminant and found in water and foods, including meats, dairy products, and...all recalled products. Wholesalers (direct customers) will be asked to immediately
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/sandoz-inc-issues-voluntary-recall-ranitidine-hydrochloride-capsules-150mg-and-300mg-due-elevated
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
...contaminant and found in water and foods, including meats, dairy products and...is notifying its distributors and direct customers by certified mail and is
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
August Egg Company Recalls Shell Eggs Because of Possible Health Risk | FDA
Lucky, Smart & Final, Safeway, Raleys, Food 4 Less and Ralphs. The eggs were also...refund. Further questions may be directed to the company at 1-800-710-2554,
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/august-egg-company-recalls-shell-eggs-because-possible-health-risk
URGENT: Nationwide Voluntary Recall of Natierra Organic Freeze- Dried Blueberry (lot # 2021363-1 & 2022026-1) Due to levels of Lead | FDA
...site is actively working to enhance food safety system by implementing mandatory...salesadmin@BrandStormInc.com or send a direct message utilizing www.Natierra.com
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/urgent-nationwide-voluntary-recall-natierra-organic-freeze-dried-blueberry-lot-2021363-1-2022026-1
Endo USA, Inc. Issues Voluntary, Nationwide Recall of Adrenalin® Chloride Solution (EPINEPHrine Nasal Solution, USP) Due to the Potential for Administration Errors | FDA
...product, which pre-dates the 1938 Federal Food, Drug & Cosmetic Act, was never submitted...providing written notification to all direct customer accounts that have received
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/endo-usa-inc-issues-voluntary-nationwide-recall-adrenalinr-chloride-solution-epinephrine-nasal
CORRECTION: Foodynamics Recalls Raw Dog Barkery, BellePepper Cats, and Kanu Pets Brand Freeze-Dried Pet Treats Because Of Possible Salmonella Contamination | FDA
...distribution and has contacted all direct customers. No adverse health effects...recalled products. Wash and sanitize pet food bowls, cups, and storage containers
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/correction-foodynamics-recalls-raw-dog-barkery-bellepepper-cats-and-kanu-pets-brand-freeze-dried-pet
Torrent Pharmaceuticals Limited Expands Voluntary Nationwide Recall of Losartan Potassium Tablets, USP | FDA
...substance that occurs naturally in certain foods, drinking water, air pollution, and...return of this product should be directed to Qualanex at 1-888-280-2040 (live
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/torrent-pharmaceuticals-limited-expands-voluntary-nationwide-recall-losartan-potassium-tablets-usp
American Regent, Inc. Issues Voluntary Nationwide Recall of Three Lots of Epinephrine Injection, USP 30 mg/ 30 mL (1 mg/mL) Due to the Presence of Particulate Matter and Lack of Assurance of Sterility | FDA
...and is to be used by or under the direction of a physician. Epinephrine Injection...result from insect stings or bites, foods, drugs, sera, diagnostic testing substances
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/american-regent-inc-issues-voluntary-nationwide-recall-three-lots-epinephrine-injection-usp-30-mg-30
UPDATED: Torrent Pharmaceuticals Limited Issues Voluntary Nationwide Recall of Losartan Potassium Tablets, USP and Losartan Potassium and Hydrochlorothiazide Tablets, USP | FDA
...substance that occurs naturally in certain foods, drinking water, air pollution, and...return of this product should be directed to Qualanex at 1-888-280-2040 (live
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/updated-torrent-pharmaceuticals-limited-issues-voluntary-nationwide-recall-losartan-potassium
Amneal Pharmaceuticals, LLC. Issues Voluntary Nationwide Recall of Ranitidine Tablets, USP, 150mg and 300mg, and Ranitidine Syrup (Ranitidine Oral Solution, USP), 15 mg/mL, Due to Possible Presence of N-nitrosodimethylamine (NDMA) Impurity | FDA
...contaminant and found in water and foods, including meats, dairy products and...Repackagers. Amneal is notifying its direct customers via mail (UPS Standard Overnight)
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/amneal-pharmaceuticals-llc-issues-voluntary-nationwide-recall-ranitidine-tablets-usp-150mg-and-300mg
Westminster Pharmaceuticals, LLC. Issues Voluntary Nationwide Recall of Levothyroxine and Liothyronine (Thyroid Tablets, USP) Due to Risk of Adulteration | FDA
...the various therapeutic measures directed at these concomitant endocrine diseases...Westminster’s direct accounts. Westminster is notifying its direct accounts by
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/westminster-pharmaceuticals-llc-issues-voluntary-nationwide-recall-levothyroxine-and-liothyronine
Henkel Corp. Announces a Nationwide Recall of Schwarzkopf Professional Osis Grip 6.76 fl. Oz/200 ml Due to Packaging Imperfection | FDA
...recall with the knowledge of the U.S. Food and Drug Administration. As part of...complete satisfaction. Questions may be directed to dedicated customer specialists
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/henkel-corp-announces-nationwide-recall-schwarzkopf-professional-osis-grip-676-fl-oz200-ml-due
Alvogen Issues Voluntary Nationwide Recall for One Lot of Fentanyl Transdermal System 25 mcg/h Due to a Defective Delivery System | FDA
...is notifying its distributors and direct customers by certified letter and is...Questions regarding this recall should be directed to Alvogen Customer Complaints by
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/alvogen-issues-voluntary-nationwide-recall-one-lot-fentanyl-transdermal-system-25-mcgh-due-defective
Working Cow Homemade, Inc. Expands Recall of Ice Cream Products Because of Possible Health Risk
...conducted in cooperation with the U.S. Food and Drug Administration (“FDA”) out...credit. Additional questions may be directed to the Working Cow Headquarters at
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/working-cow-homemade-inc-expands-recall-ice-cream-products-because-possible-health-risk
Amneal Pharmaceuticals LLC Issues Voluntary Nationwide Recall of Metformin Hydrochloride Extended Release Tablets, USP, 500 mg and 750 mg, Due to Detection of N-Nitrosodimethylamine (NDMA) Impurity | FDA
...environmental contaminant found in water and foods, including meats, dairy products and...Repackagers. Amneal is notifying its direct customers via mail (UPS Standard Overnight)
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/amneal-pharmaceuticals-llc-issues-voluntary-nationwide-recall-metformin-hydrochloride-extended
Motivate Me Ashley, LLC is Recalling VidaSlim Brand 90-Day, 30-day and 7-Day Original Root, Root Plus, and Root Capsules & VidaSlim Hot Body Brew Due to the Presence of Yellow Oleander in the Products | FDA
...sold at www.vidaslim.com and through direct sales via independent distributors...conducted with the knowledge of the U.S. Food and Drug Administration. Consumers who
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/motivate-me-ashley-llc-recalling-vidaslim-brand-90-day-30-day-and-7-day-original-root-root-plus-and
Par Health Issues Voluntary Nationwide Recall of Argatroban Injection Due to the Presence of Particulate Matter | FDA
Injection 250 mg/2.5 mL (100 mg/mL) is a direct thrombin inhibitor indicated for prophylaxis...Questions regarding this recall can be directed to Inmar, Inc. at 1-855-648-7909 Monday
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/par-health-issues-voluntary-nationwide-recall-argatroban-injection-due-presence-particulate-matter
Hi Tech Pharmaceuticals Issues Voluntary Recall on Lipodrene w/25mg Ephedra Extract Dietary Supplement Due to the Presence of 1,4-dimethylamylamine (DMAA) | FDA
Heart attack. ( https://www.fda.gov/food/dietary-supplement-products-ingredi...distributed through wholesale and direct sales in the U.S. and Puerto Rico,
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/hi-tech-pharmaceuticals-issues-voluntary-recall-lipodrene-w25mg-ephedra-extract-dietary-supplement
Working Cow Homemade, Inc. Recalls Product Because of Possible Health Risk
...conducted in cooperation with the U.S. Food and Drug Administration (“FDA”) following...credit. Additional questions may be directed to the Working Cow Headquarters at
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/working-cow-homemade-inc-recalls-product-because-possible-health-risk