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Search Results for Nationwide recall

Showing results 681 - 700 of 973 for Nationwide recall.

MBI Distributing, Inc. Issues Voluntary Nationwide Recall of Homeopathic Teething Drops, Nausea Drops, Intestinal Colic Drops, Stomach Calm, Expectorant Cough Syrup, Silver-Zinc Throat Spray, and Argentum Elixir Due to a Lack of Process Controls | FDA

This recall has been completed and FDA has terminated this recall....Distributing, Inc. Issues Voluntary Nationwide Recall of Homeopathic Teething Drops...Controls This recall has been completed and FDA has terminated this recall. When a
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/mbi-distributing-inc-issues-voluntary-nationwide-recall-homeopathic-teething-drops-nausea-drops

Camber Pharmaceuticals, Inc. Issues Voluntary Nationwide Recall of Valsartan Tablets, USP, 40mg, 80mg, 160mg and 320mg Due to The Detection of Trace Amounts of N-Nitrosodimethylamine (NDMA) Impurity, Found in an Active Pharmaceutical Ingredient (API) | FDA

This recall has been completed and FDA has terminated this recall....Pharmaceuticals, Inc. Issues Voluntary Nationwide Recall of Valsartan Tablets, USP, 40mg...(API) This recall has been completed and FDA has terminated this recall. When a
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/camber-pharmaceuticals-inc-issues-voluntary-nationwide-recall-valsartan-tablets-usp-40mg-80mg-160mg

Fresenius Kabi Issues Voluntary Nationwide Recall of Midazolam Injection, USP, 2 mg/2 mL Due to Reports of Blister Packages Containing Syringes of Ondansetron Injection, USP, 4 mg/2 mL | FDA

This recall has been completed and FDA has terminated this recall....Fresenius Kabi Issues Voluntary Nationwide Recall of Midazolam Injection, USP,...mL This recall has been completed and FDA has terminated this recall. When a
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/fresenius-kabi-issues-voluntary-nationwide-recall-midazolam-injection-usp-2-mg2-ml-due-reports

Biota Biosciences Issues Voluntary Nationwide Recall of Cannabidiol (CBD) Complex, Curcumin Complex, and Cannabidiol + Curcumin Injectables Because They Were Marketed Without FDA Approval | FDA

Biota Biosciences is voluntarily recalling the following lots in the table below...Biosciences Issues Voluntary Nationwide Recall of Cannabidiol (CBD) Complex...Approval When a company announces a recall, market withdrawal, or safety alert
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/biota-biosciences-issues-voluntary-nationwide-recall-cannabidiol-cbd-complex-curcumin-complex-and

Janssen Issues Voluntary Nationwide Recall for One Lot of ORTHO-NOVUM 1/35 and Two Lots of ORTHO-NOVUM 7/7/7 Due to Incorrect Veridate Dispenser Instructions | FDA

This recall has been completed and FDA has terminated this recall....ANNOUNCEMENT Janssen Issues Voluntary Nationwide Recall for One Lot of ORTHO-NOVUM 1/35...Instructions This recall has been completed and FDA has terminated this recall. When a
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/janssen-issues-voluntary-nationwide-recall-one-lot-ortho-novum-135-and-two-lots-ortho-novum-777-due

J&J Distributing (owned by New Harvest Foods) Recalls Multiple Products Because of Possible Health Risk | FDA

Distributing of St. Paul, MN, is recalling multiple products because they have...Distributing (owned by New Harvest Foods) Recalls Multiple Products Because of Possible...Health Risk When a company announces a recall, market withdrawal, or safety alert
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/jj-distributing-owned-new-harvest-foods-recalls-multiple-products-because-possible-health-risk

Royal International Trading Inc Issues Alert On Undeclared Sulfites In “Tayni Boctoka Dry Fruits Mix Compot Apple” | FDA

This recall has been completed and FDA has terminated this recall....Apple” 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/royal-international-trading-inc-issues-alert-undeclared-sulfites-tayni-boctoka-dry-fruits-mix-compot

A&H Focal Inc. Issues Nationwide Recall of 21 Products Marketed as Dietary Supplements & One Cosmetic Product Due to the Possible Presence of Undeclared Erectile Dysfunction Ingredients | FDA

This recall has been completed and FDA has terminated this recall....ANNOUNCEMENT A&H Focal Inc. Issues Nationwide Recall of 21 Products Marketed as Dietary...Ingredients This recall has been completed and FDA has terminated this recall. When a
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/ah-focal-inc-issues-nationwide-recall-21-products-marketed-dietary-supplements-one-cosmetic-product

Sciegen Pharmaceuticals, Inc. Issues Voluntary Nationwide Recall of Irbesartan Tablets, USP 75 Mg, 150 Mg, and 300 Mg Due to The Detection of Trace Amounts of NDEA (N-Nitrosodiethylamine) Impurity Found in The Active Pharmaceutical Ingredient (API) | FDA

This recall has been completed and FDA has terminated this recall....Pharmaceuticals, Inc. Issues Voluntary Nationwide Recall of Irbesartan Tablets, USP 75...(API) This recall has been completed and FDA has terminated this recall. When a
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/sciegen-pharmaceuticals-inc-issues-voluntary-nationwide-recall-irbesartan-tablets-usp-75-mg-150-mg

Astrazeneca Initiates Voluntary Nationwide Recall of One Lot of Brilinta 90 mg Professional Sample Bottles Due to Report of Another Medicine in One Bottle From That Lot | FDA

This recall has been completed and FDA has terminated this recall....Astrazeneca Initiates Voluntary Nationwide Recall of One Lot of Brilinta 90 mg...Lot This recall has been completed and FDA has terminated this recall. When a
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/astrazeneca-initiates-voluntary-nationwide-recall-one-lot-brilinta-90-mg-professional-sample-bottles

Advanced Pharma, Inc. d/b/a Avella of Houston Issues Voluntary Nationwide Recall of Specific Lots of Potassium Phosphate and Succinylcholine Repacked and/or Compounded at its Houston Location as a Result of Hospira, Inc’s June 15, 2017 Recall of Such Pro | FDA

This recall has been completed and FDA has terminated this recall....Avella of Houston Issues Voluntary Nationwide Recall of Specific Lots of Potassium...Hospira, Inc’s June 15, 2017 Recall of Such Pro This recall has been completed and
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/advanced-pharma-inc-dba-avella-houston-issues-voluntary-nationwide-recall-specific-lots-potassium

Teva Pharmaceuticals, USA Extends Voluntary Nationwide Recall to Consumer/User Level for One Lot of Paliperidone Extended-Release Tablets, 3mg, 90 Count Bottles Distributed Under the Actavis Pharma Inc. Label Due to Dissolution Test Failure | FDA

This recall has been completed and FDA has terminated this recall....Pharmaceuticals, USA Extends Voluntary Nationwide Recall to Consumer/User Level for One...Failure This recall has been completed and FDA has terminated this recall. When a
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/teva-pharmaceuticals-usa-extends-voluntary-nationwide-recall-consumeruser-level-one-lot-paliperidone

Hospira Issues a Voluntary Nationwide Recall For 8.4% Sodium Bicarbonate Injection, USP, Neut tm (Sodium Bicarbonate 4% Additive Solution), QUELICIN tm (Succinylcholine Chloride Injection, USP) and Potassium Phosphates Injection, US | FDA

This recall has been completed and FDA has terminated this recall....ANNOUNCEMENT Hospira Issues a Voluntary Nationwide Recall For 8.4% Sodium Bicarbonate Injection...US This recall has been completed and FDA has terminated this recall. When a
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/hospira-issues-voluntary-nationwide-recall-84-sodium-bicarbonate-injection-usp-neut-tm-sodium

Rong Shing Trading Ny Inc. Issues Allergy Alert on Undeclared Milk in Ganchi Naiweitangpian Candies | FDA

This recall has been completed and FDA has terminated this recall....Candies 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/rong-shing-trading-ny-inc-issues-allergy-alert-undeclared-milk-ganchi-naiweitangpian-candies

Endo Pharmaceuticals Inc. Issues Voluntary Nationwide Recall for One Lot of Edex® (alprostadil for injection) 10 mcg 2 Pack Carton Due to Potential Lack of Sterility Assurance | FDA

This recall has been completed and FDA has terminated this recall....Pharmaceuticals Inc. Issues Voluntary Nationwide Recall for One Lot of Edex® (alprostadil...Assurance This recall has been completed and FDA has terminated this recall. When a
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/endo-pharmaceuticals-inc-issues-voluntary-nationwide-recall-one-lot-edexr-alprostadil-injection-10

Heritage Pharmaceuticals Inc. Issues Voluntary Nationwide Recall of Amikacin Sulfate Injection, USP 1gm/4 mL (250mg/mL) and Prochlorperazine Edisylate Injection, USP 10mg/2mL (5mg/mL) as a Result of a Sterility Test Failure | FDA

This recall has been completed and FDA has terminated this recall....Pharmaceuticals Inc. Issues Voluntary Nationwide Recall of Amikacin Sulfate Injection...Failure This recall has been completed and FDA has terminated this recall. More Recalls
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/heritage-pharmaceuticals-inc-issues-voluntary-nationwide-recall-amikacin-sulfate-injection-usp-1gm4

Lupin Pharmaceuticals Inc. Announces a Nationwide Recall of Mibelas™ 24 Fe (Norethindrone Acetate and EthinylEstradiol 1mg/0.02mg Chewable Tablets and Ferrous Fumarate 75 mg) Tablets Due to Out of Sequence Tablets and Missing Expiry/Lot Information | FDA

This recall has been completed and FDA has terminated this recall....Pharmaceuticals Inc. Announces a Nationwide Recall of Mibelas™ 24 Fe (Norethindrone...Information 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-announces-nationwide-recall-mibelastm-24-fe-norethindrone-acetate-and

Kader Exports Recalls Frozen Cooked Shrimp Because of Possible Health Risk | FDA

...with an abundance of caution, is recalling certain consignments of various sizes...The product has been distributed nationwide from late February 2020 to Mid-May...COMPANY ANNOUNCEMENT Kader Exports Recalls Frozen Cooked Shrimp Because of Possible...Health Risk When a company announces a recall, market withdrawal, or safety alert
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/kader-exports-recalls-frozen-cooked-shrimp-because-possible-health-risk

Advanced Pharma, Inc. D/B/A Avella of Houston Issues Voluntary Nationwide Recall of All Unexpired Nitroglycerin Injection In 5% Dextrose USP Products Produced At Its Houston Location From March 3, 2017 Through May 31, 2017 Due To Sub-Potency | FDA

This recall has been completed and FDA has terminated this recall....Avella of Houston Issues Voluntary Nationwide Recall of All Unexpired Nitroglycerin...Sub-Potency This recall has been completed and FDA has terminated this recall. When a
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/advanced-pharma-inc-dba-avella-houston-issues-voluntary-nationwide-recall-all-unexpired

Med Man Issues Voluntary Nationwide Recall of Up2 Due to Presence of Undeclared Sildenafil | FDA

Med Man Distribution is voluntarily recalling all lots of Up2 Dietary supplement...ANNOUNCEMENT Med Man Issues Voluntary Nationwide Recall of Up2 Due to Presence of Undeclared...Sildenafil When a company announces a recall, market withdrawal, or safety alert
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/med-man-issues-voluntary-nationwide-recall-up2-due-presence-undeclared-sildenafil