Search Results for Nationwide recall
Showing results 181 - 200 of 975 for Nationwide recall.
nanoMaterials Discovery Corporation Issues Voluntary Nationwide Recall of its Alcohol Antiseptic 80% Alcohol Solution | FDA
Discovery Corporation is voluntarily recalling all lots of its Alcohol Antiseptic...Corporation Issues Voluntary Nationwide Recall of its Alcohol Antiseptic 80%...Solution When a company announces a recall, market withdrawal, or safety alert
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/nanomaterials-discovery-corporation-issues-voluntary-nationwide-recall-its-alcohol-antiseptic-80
Je Dois L’avoir Boutique Issues Voluntary Nationwide Recall of 365 Skinny High Intensity and 365 Skinny Emergency Boutique Due to the Presence of Sibutramine | FDA
This recall has been completed and FDA has terminated this recall....L’avoir Boutique Issues Voluntary Nationwide Recall of 365 Skinny High Intensity...Sibutramine This recall has been completed and FDA has terminated this recall. When a
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/je-dois-lavoir-boutique-issues-voluntary-nationwide-recall-365-skinny-high-intensity-and-365-skinny
G.A. Mart Issues Voluntary Nationwide Recall of H&NATURAL TejoRoot and H&NATURAL Brazil Seed Dietary Supplements Due to the Presence of Yellow Oleander (Thevetia peruviana), a Poisonous Plant Native to Mexico and Central America | FDA
Mart dba H&Natural, is voluntarily recalling 2 lots of H&NATURAL TejoRoot, 10g...ANNOUNCEMENT G.A. Mart Issues Voluntary Nationwide Recall of H&NATURAL TejoRoot and H&NATURAL...America When a company announces a recall, market withdrawal, or safety alert
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/ga-mart-issues-voluntary-nationwide-recall-hnatural-tejoroot-and-hnatural-brazil-seed-dietary
Ata Int. Inc. Issues Voluntary Nationwide Recall of BLUEFUSION Capsules, Due to presence of Undeclared Sildenafil, Tadalafil, Desmethyl carbodenafil, Dithiodesmethyl carbodenafil, Scutellarin and Daidzein | FDA
This recall has been completed and FDA has terminated this recall....Ata Int. Inc. Issues Voluntary Nationwide Recall of BLUEFUSION Capsules, Due to...Daidzein This recall has been completed and FDA has terminated this recall. When a
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/ata-int-inc-issues-voluntary-nationwide-recall-bluefusion-capsules-due-presence-undeclared
Hospira, Inc. Issues A Voluntary Nationwide Recall For 4.2% Sodium Bicarbonate Injection, 8.4% Sodium Bicarbonate Injection, and Atropine Sulfate Injection Due to the Potential Presence of Glass Particulate Matter | FDA
...a Pfizer company, is voluntarily recalling the lots listed in the table below...Hospira, Inc. Issues A Voluntary Nationwide Recall For 4.2% Sodium Bicarbonate Injection...Matter When a company announces a recall, market withdrawal, or safety alert
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/hospira-inc-issues-voluntary-nationwide-recall-42-sodium-bicarbonate-injection-84-sodium-bicarbonate
Fabalish Inc. Recalls “Kickin’ Carrot Falafel Bites” Because of Possible Health Risk | FDA
This recall has been completed and FDA has terminated this recall....COMPANY ANNOUNCEMENT Fabalish Inc. Recalls “Kickin’ Carrot Falafel Bites” Because...Risk This recall has been completed and FDA has terminated this recall. When a
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/fabalish-inc-recalls-kickin-carrot-falafel-bites-because-possible-health-risk
Global Pharma Healthcare Issues Voluntary Nationwide Recall of Artificial Tears Lubricant Eye Drops Due to Possible Contamination | FDA
Pharma Healthcare is voluntarily recalling all lots within expiry of their Artificial...Pharma Healthcare Issues Voluntary Nationwide Recall of Artificial Tears Lubricant...Contamination When a company announces a recall, market withdrawal, or safety alert
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/global-pharma-healthcare-issues-voluntary-nationwide-recall-artificial-tears-lubricant-eye-drops-due
Lupin Pharmaceuticals, Inc. Issues Voluntarily Nationwide Recall of All Irbesartan Tablets and Irbesartan and Hydrochlorothiazide Tablets Due to Potential Presence of N-nitrosoirbesartan Impurity | FDA
This recall has been completed and FDA has terminated this recall....Pharmaceuticals, Inc. Issues Voluntarily Nationwide Recall of All Irbesartan Tablets and...Impurity This recall has been completed and FDA has terminated this recall. When a
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/lupin-pharmaceuticals-inc-issues-voluntarily-nationwide-recall-all-irbesartan-tablets-and-irbesartan
Hospira, Inc. Issues A Voluntary Nationwide Recall For One Lot of Bleomycin for Injection, USP 15 Units Single Dose ONCO-TAIN™ Glass Fliptop Vial Due To The Potential For Presence of Glass Particulate Matter | FDA
...a Pfizer company, is voluntarily recalling one lot of Bleomycin for Injection...lot BL12206A, to the user level. The recall was initiated due to a confirmed customer...Hospira, Inc. Issues A Voluntary Nationwide Recall For One Lot of Bleomycin for...Matter When a company announces a recall, market withdrawal, or safety alert
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/hospira-inc-issues-voluntary-nationwide-recall-one-lot-bleomycin-injection-usp-15-units-single-dose
Alembic Pharmaceuticals Limited Issues Voluntary Nationwide Recall of Telmisartan Tablets, USP, 20 mg Due to Label Mix-Up | FDA
This recall has been completed and FDA has terminated this recall....Pharmaceuticals Limited Issues Voluntary Nationwide Recall of Telmisartan Tablets, USP,...Mix-Up This recall has been completed and FDA has terminated this recall. When a
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/alembic-pharmaceuticals-limited-issues-voluntary-nationwide-recall-telmisartan-tablets-usp-20-mg-due
B. Braun Medical Inc. Issues Voluntary Nationwide Recall of 0.9% Sodium Chloride for Injection USP 250ML in Excel Due to Fluid Leakage or Low Fill Volume | FDA
This recall has been completed and FDA has terminated this recall....Medical Inc. Issues Voluntary Nationwide Recall of 0.9% Sodium Chloride for Injection...Volume This recall has been completed and FDA has terminated this recall. When a
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/b-braun-medical-inc-issues-voluntary-nationwide-recall-09-sodium-chloride-injection-usp-250ml-excel
Fusion Health and Vitality Issues Voluntary Nationwide Recall of Core Essential Nutrients and Immune Boost Sublingual Vitamin D3 Due to the Unapproved Use of a Food Additive and Unapproved Marketing Statements | FDA
This recall has been completed and FDA has terminated this recall....and Vitality Issues Voluntary Nationwide Recall of Core Essential Nutrients and...Statements This recall has been completed and FDA has terminated this recall. When a
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/fusion-health-and-vitality-issues-voluntary-nationwide-recall-core-essential-nutrients-and-immune
TDBBS LLC Recalls Green Tripe Dog Treats Due to Potential Foreign Metal Object Contamination | FDA
This recall has been completed and FDA has terminated this recall....COMPANY ANNOUNCEMENT TDBBS LLC Recalls Green Tripe Dog Treats Due to Potential...Contamination This recall has been completed and FDA has terminated this recall. When a
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/tdbbs-llc-recalls-green-tripe-dog-treats-due-potential-foreign-metal-object-contamination
Acella Pharmaceuticals, LLC Issues Voluntary Nationwide Recall of Two Lots of NP Thyroid®, Thyroid Tablets, USP Due to Sub Potency | FDA
This recall has been completed and FDA has terminated this recall....Pharmaceuticals, LLC Issues Voluntary Nationwide Recall of Two Lots of NP Thyroid®, Thyroid...Potency This recall has been completed and FDA has terminated this recall. When a
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/acella-pharmaceuticals-llc-issues-voluntary-nationwide-recall-two-lots-np-thyroidr-thyroid-tablets
UPDATE - Akorn Issues Voluntary Nationwide Recall of Various Human and Animal Drug Products Within Expiry Due to Company Shutdown | FDA
Trustee is initiating a voluntary recall of various w...UPDATE - Akorn Issues Voluntary Nationwide Recall of Various Human and Animal Drug...Shutdown When a company announces a recall, market withdrawal, or safety alert
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/update-akorn-issues-voluntary-nationwide-recall-various-human-and-animal-drug-products-within-expiry
Major Pharmaceuticals Issues Voluntary Nationwide Recall of Valsartan Due to the Potential Presence of a Probable Carcinogen (NDMA) | FDA
This recall has been completed and FDA has terminated this recall....Pharmaceuticals Issues Voluntary Nationwide Recall of Valsartan Due to the Potential...(NDMA) This recall has been completed and FDA has terminated this recall. When a
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/major-pharmaceuticals-issues-voluntary-nationwide-recall-valsartan-due-potential-presence-probable
Global Pharma Healthcare Issues Voluntary Nationwide Recall of Delsam Pharma Artificial Eye Ointment Due to Possible Microbial Contamination | FDA
Pharma Healthcare is voluntarily recalling Batch No. H29 of Artificial Eye Ointment...Pharma Healthcare Issues Voluntary Nationwide Recall of Delsam Pharma Artificial Eye...Contamination When a company announces a recall, market withdrawal, or safety alert
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/global-pharma-healthcare-issues-voluntary-nationwide-recall-delsam-pharma-artificial-eye-ointment
Beaumont Bio Med, Inc. Issues Voluntary Nationwide Recall of all their Homeopathic Aqueous/Alcohol-Based Medicines Due to the Nationwide Recall by the Contract Manufacturer, King Bio, of all their Aqueous-Based Products Due to Possible Microbial Contamination | FDA
This recall has been completed and FDA has terminated this recall....Bio Med, Inc. Issues Voluntary Nationwide Recall of all their Homeopathic Aqueous/Alcohol-Based...Aqueous/Alcohol-Based Medicines Due to the Nationwide Recall by the Contract Manufacturer
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/beaumont-bio-med-inc-issues-voluntary-nationwide-recall-all-their-homeopathic-aqueousalcohol-based
Tris Pharma, Inc Expands Its Voluntary Nationwide Retail Recall of Ibuprofen Oral Suspension Drops, USP, 50 mg per 1.25 mL, Due to Higher Concentration of Ibuprofen | FDA
This recall has been completed and FDA has terminated this recall....Inc Expands Its Voluntary Nationwide Retail Recall of Ibuprofen Oral Suspension...Ibuprofen This recall has been completed and FDA has terminated this recall. When a
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/tris-pharma-inc-expands-its-voluntary-nationwide-retail-recall-ibuprofen-oral-suspension-drops-usp
Dr. Berne’s Whole Health Products Issues Voluntary Nationwide Recall of Dr. Berne’s MSM Drops 5% and 15% Solution Eye Drops Due to Bacterial and Fungal Contamination | FDA
Whole Health Products is voluntarily recalling all lots of MSM DROPS 5%,15% Solution...Health Products Issues Voluntary Nationwide Recall of Dr. Berne’s MSM Drops 5% and...Contamination When a company announces a recall, market withdrawal, or safety alert
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/dr-bernes-whole-health-products-issues-voluntary-nationwide-recall-dr-bernes-msm-drops-5-and-15