Search Results for FOOD DIRECTIONS
Showing results 61 - 80 of 104 for FOOD DIRECTIONS.
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
Amneal Pharmaceuticals, LLC. Issues Voluntary Nationwide Recall of Nizatidine Oral Solution, 15 mg/mL, Due to Potential Levels of N-nitrosodimethylamine (NDMA) Impurity Amounts Above the Levels Established by FDA | FDA
...contaminant and found in water and foods, including meats, dairy products and...in the USA. Amnealis notifying its direct customers by mailing (FED Ex Standard
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/amneal-pharmaceuticals-llc-issues-voluntary-nationwide-recall-nizatidine-oral-solution-15-mgml-due
Supreme Service Solutions LLC Voluntarily Recalls Supreme Produce Cucumber Products Because of Possible Health Risk | FDA
...initiated their recall after the US Food and Drug Administration (“FDA”) notified...SunFed is also contacting each of its direct buyers to advise them of the recall
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/supreme-service-solutions-llc-voluntarily-recalls-supreme-produce-cucumber-products-because-possible
Yummi Sushi LLC Voluntarily Recalls Cucumber Products Because of Possible Health Risk | FDA
...initiated their recall after the US Food and Drug Administration (“FDA”) notified...SunFed is also contacting each of its direct buyers to advise them of the recall
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/yummi-sushi-llc-voluntarily-recalls-cucumber-products-because-possible-health-risk
Greenwich Rx Issues Voluntary Nationwide Recall of Compounded Glutathione Due to Elevated Endotoxin Levels | FDA
...healthcare provider. Customers can direct questions regarding this recall to...conducted with the knowledge of the U.S. Food and Drug Administration.
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/greenwich-rx-issues-voluntary-nationwide-recall-compounded-glutathione-due-elevated-endotoxin-levels
Sprayology Issues Voluntary Nationwide Recall of Homeopathic Aqueous-Based Medicines Due to Microbial Contamination | FDA
Sprayology is notifying its retailers and direct consumers by letter and is arranging...conducted with the knowledge of the U.S. Food and Drug Administration.
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/sprayology-issues-voluntary-nationwide-recall-homeopathic-aqueous-based-medicines-due-microbial
Church & Dwight Co., Inc. Issues Voluntary Nationwide Recall of Zicam® Cold Remedy Nasal Swabs, Zicam® Nasal AllClear Swabs, and Orajel™ Baby Teething Swabs Due to Microbial Contamination | FDA
...additional questions can also be directed to its Consumer Relations team Monday...conducted with the knowledge of the U.S. Food and Drug Administration. This recall
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/church-dwight-co-inc-issues-voluntary-nationwide-recall-zicamr-cold-remedy-nasal-swabs-zicamr-nasal
Denton Pharma, Inc. dba Northwind Pharmaceuticals Voluntarily Recalls All Unexpired Lots of its Ranitidine Tablets and Ceases Distribution, Due to Possible Presence of N-nitrosodimethylamine (NDMA) Impurity | FDA
...below. Northwind is notifying its direct customers with a recall notification...conducted with the knowledge of the U.S. Food and Drug Administration.
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/denton-pharma-inc-dba-northwind-pharmaceuticals-voluntarily-recalls-all-unexpired-lots-its
Pfizer Issues a Voluntary Nationwide Recall for Twelve Lots of CHANTIX® (Varenicline) Tablets Due to N-Nitroso Varenicline Content | FDA
Nitrosamines are common in water and foods, including cured and grilled meats...process. Pfizer has notified their direct consignees by letter to arrange for
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/pfizer-issues-voluntary-nationwide-recall-twelve-lots-chantixr-varenicline-tablets-due-n-nitroso
Pfizer Expands Voluntary Nationwide Recall to include Four Additional Lots of CHANTIX® (varenicline) Tablets Due to N- Nitroso Varenicline Content | FDA
Nitrosamines are common in water and foods, including cured and grilled meats...process. Pfizer has notified their direct consignees by letter to arrange for
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/pfizer-expands-voluntary-nationwide-recall-include-four-additional-lots-chantixr-varenicline-tablets
American Regent, Inc. Issues Voluntary Nationwide Recall of One Lot of Papaverine Hydrochloride Injection, USP 60 mg/ 2 mL Due to the Presence of Visible Particulate Matter | FDA
...and is to be used by or under the direction of a physician. Patients that use...conducted with the knowledge of the U.S. Food and Drug Administration. American Regent
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/american-regent-inc-issues-voluntary-nationwide-recall-one-lot-papaverine-hydrochloride-injection
Koikoi Trading Inc., Issues Allergy Alert on Undeclared Wheat and Sesame in FU ZHOU FISH BALL (200g / 400g / 5lb)
...may have reached consumers through direct delivery to restaurant customers, distributors...made with the knowledge of the U.S. Food and Drug Administration (FDA). What
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/koikoi-trading-inc-issues-allergy-alert-undeclared-wheat-and-sesame-fu-zhou-fish-ball-200g-400g-5lb
Nostrum Laboratories, Inc. Issues Voluntary Nationwide Recall of Sucralfate Tablets USP 1 Gram Within Expiry | FDA
...is notifying its distributors and direct consignees for this product by email...conducted with the knowledge of the U.S. Food and Drug Administration.
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/nostrum-laboratories-inc-issues-voluntary-nationwide-recall-sucralfate-tablets-usp-1-gram-within
Global Mix, Inc Recalls Tejocote Products Because of Possible Health Risk | FDA
...posted by the FDA https://www.fda.gov/food/alerts-advisories-safety-informatio...via the below websites via courier direct delivery and mail order. Etsy.com amazon
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/global-mix-inc-recalls-tejocote-products-because-possible-health-risk
American Regent, Inc. Animal Health Issues Nationwide Recall of Two Lots of Adequan® Canine and Two Lots of Adequan® I.M. Due to Visible Glass Fiber Material in the Product | FDA
...and are to be used by or under the direction of a licensed veterinarian. Adequan...conducted with the knowledge of the U.S. Food and Drug Administration. American Regent
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/american-regent-inc-animal-health-issues-nationwide-recall-two-lots-adequanr-canine-and-two-lots
Unique Pharmaceutical Laboratories (A Div. of J. B. Chemicals & Pharmaceuticals Ltd.) Issues Voluntary Nationwide Recall of Cetirizine Hydrochloride Tablets USP 5 mg Due to Potential Cross Contamination with Ranitidine | FDA
...has notified its distributors and direct customers by email and is arranging...conducted with the knowledge of the U.S. Food and Drug Administration.
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/unique-pharmaceutical-laboratories-div-j-b-chemicals-pharmaceuticals-ltd-issues-voluntary-nationwide
Par Health Issues Voluntary Nationwide Recall of Two Lots of Brevital® Sodium 500 mg/vial CIV (Methohexital Sodium for Injection, USP) Due to the Presence of Particulate Matter | FDA
Questions regarding this recall can be directed to Inmar, Inc. at 1-844-774-1187 Monday...conducted with the knowledge of the U.S. Food and Drug Administration. Package Identification:
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/par-health-issues-voluntary-nationwide-recall-two-lots-brevitalr-sodium-500-mgvial-civ-methohexital
Pfizer Expands Voluntary Nationwide Recall to include All Lots of CHANTIX® (Varenicline) Tablets Due to N-Nitroso Varenicline Content | FDA
Nitrosamines are common in water and foods, including cured and grilled meats...process. Pfizer has notified their direct consignees by letter to arrange for
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/pfizer-expands-voluntary-nationwide-recall-include-all-lots-chantixr-varenicline-tablets-due-n
Cardinal Health, Inc. Issues Voluntary Nationwide Recall of Certain LEADER™ Brand Eye Drops Supplied by Velocity Pharma, LLC Due to Potential Risk of Eye Infections | FDA
Health, Inc. is notifying all impacted direct accounts via mail of this voluntary...conducted with the knowledge of the U.S. Food and Drug Administration.
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/cardinal-health-inc-issues-voluntary-nationwide-recall-certain-leadertm-brand-eye-drops-supplied
Kadesh Incorporation Issues Voluntary Nationwide Recall of Puriton Eye Relief Drops Due to Non-Sterile Production Conditions | FDA
...product is relatively high and can cause direct destruction of tissues in the cornea...conducted with the knowledge of the U.S. Food and Drug Administration.
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/kadesh-incorporation-issues-voluntary-nationwide-recall-puriton-eye-relief-drops-due-non-sterile