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Showing results 201 - 220 of 975 for Nationwide recall.

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

Moor Herbs Recalls “Angel Formula” Infant Formula Because of Possible Health Risk | FDA

This recall has been completed and FDA has terminated this recall....COMPANY ANNOUNCEMENT Moor Herbs Recalls “Angel Formula” Infant Formula 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/moor-herbs-recalls-angel-formula-infant-formula-because-possible-health-risk

MPM Medical LLC Issues Voluntary Nationwide Recall of Regenecare HA Hydrogel Due to Burkholderia cepecia Contamination | FDA

This recall has been completed and FDA has terminated this recall....Medical LLC Issues Voluntary Nationwide Recall of Regenecare HA Hydrogel Due...Contamination This recall has been completed and FDA has terminated this recall. When a
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/mpm-medical-llc-issues-voluntary-nationwide-recall-regenecare-ha-hydrogel-due-burkholderia-cepecia

Adam’s Polishes, LLC Issues Voluntary Nationwide Recall of Hand Sanitizer Due to Potential Contamination With Methanol | FDA

Adam’s Polishes, LLC is voluntarily recalling lot 133475 of Adam’s Polishes Hand...undeclared methanol. Adam’s Polishes is recalling 19 other lots in an abundance of...Polishes, LLC Issues Voluntary Nationwide Recall of Hand Sanitizer Due to Potential...Methanol When a company announces a recall, market withdrawal, or safety alert
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/adams-polishes-llc-issues-voluntary-nationwide-recall-hand-sanitizer-due-potential-contamination

Scentsational Soaps & Candles, Inc. Issues Voluntary Nationwide Recall of Scented Hand Sanitizers Due to the Presence of Methanol (Wood Alcohol), Benzene and Acetaldehyde | FDA

This recall has been completed and FDA has terminated this recall....Candles, Inc. Issues Voluntary Nationwide Recall of Scented Hand Sanitizers Due...Acetaldehyde This recall has been completed and FDA has terminated this recall. When a
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/scentsational-soaps-candles-inc-issues-voluntary-nationwide-recall-scented-hand-sanitizers-due

Bindle Bottle Issues Voluntary Recall on 32 Oz, 24 Oz, 20 Oz, and 13 Oz Insulated Food and Drink Bottles | FDA

This recall has been completed and FDA has terminated this recall....ANNOUNCEMENT Bindle Bottle Issues Voluntary Recall on 32 Oz, 24 Oz, 20 Oz, and 13 Oz Insulated...Bottles This recall has been completed and FDA has terminated this recall. When a
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/bindle-bottle-issues-voluntary-recall-32-oz-24-oz-20-oz-and-13-oz-insulated-food-and-drink-bottles

Exela Pharma Sciences, LLC Issues Voluntary Nationwide Recall of 8.4% Sodium Bicarbonate Injection, USP, 50 mEq/50 mL, Midazolam in 0.8% Sodium Chloride Injection 100 mg/100 mL, and ELCYS (cysteine hydrochloride Injection), USP 500 mg/10 mL Due to the Presence of Particulate Matter | FDA

Sciences, LLC, (Exela) is voluntarily recalling the products listed in the table...Sciences, LLC Issues Voluntary Nationwide Recall of 8.4% 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/exela-pharma-sciences-llc-issues-voluntary-nationwide-recall-84-sodium-bicarbonate-injection-usp-50

Fresenius Kabi Issues Voluntary Nationwide Recall of a Single Lot of Dexmedetomidine Hydrochloride Injection Due to Cross-Contamination of Lidocaine | FDA

This recall has been completed and FDA has terminated this recall....Fresenius Kabi Issues Voluntary Nationwide Recall of a Single Lot of Dexmedetomidine...Lidocaine 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-single-lot-dexmedetomidine-hydrochloride-injection

Hofood99 Inc Recalls Enoki Mushroom Due to Possible Health Risk | FDA

Hofood99 Inc of Brooklyn, NY 11231 is recalling its 200g packages of Enoki Mushroom...COMPANY ANNOUNCEMENT Hofood99 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/hofood99-inc-recalls-enoki-mushroom-due-possible-health-risk

Feel Good Foods Issues Voluntary Recall of Gluten-Free Cream Cheese Stuffed Mini Bagels | FDA

This recall has been completed and FDA has terminated this recall....Voluntary Recall of Gluten-Free Cream Cheese Stuffed Mini Bagels This recall has been...has terminated this recall. When a company announces a recall, market withdrawal
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/feel-good-foods-issues-voluntary-recall-gluten-free-cream-cheese-stuffed-mini-bagels

Apotex Corp. Issues Voluntary Nationwide Recall of Brimonidine Tartrate Ophthalmic Solution, 0.15% Due to Cracks that Have Developed in Some of the Units Caps of the Bottles | FDA

US FDA, is initiating a voluntary recall at the Consumer level for six (6) lots...Solution, 0.15% specified below. This recall is being initiated out of an abundance...Apotex Corp. Issues Voluntary Nationwide Recall of Brimonidine Tartrate Ophthalmic...Bottles When a company announces a recall, market withdrawal, or safety alert
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/apotex-corp-issues-voluntary-nationwide-recall-brimonidine-tartrate-ophthalmic-solution-015-due

Hospira Issues Voluntary Nationwide Recall of Daptomycin for Injection Lyophilized Powder for Solution, Due to Infusion Reactions | FDA

This recall has been completed and FDA has terminated this recall....ANNOUNCEMENT Hospira Issues Voluntary Nationwide Recall of Daptomycin for Injection Lyophilized...Reactions 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-daptomycin-injection-lyophilized-powder-solution-due

KVK-Tech, Inc. Issues Voluntary Nationwide Recall of One Lot of Betaxolol Tablets, USP 10 mg (Batch Number: 17853A) as a Precautionary Measure Due to a Single Foreign Tablet Found During the Line Clearance After the Batch was Packaged | FDA

Pennsylvania, KVK-Tech, Inc. is voluntarily recalling one lot (Batch Number: 17853A; “the...KVK-Tech, Inc. Issues Voluntary Nationwide Recall of One Lot of Betaxolol Tablets...Packaged When a company announces a recall, market withdrawal, or safety alert
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/kvk-tech-inc-issues-voluntary-nationwide-recall-one-lot-betaxolol-tablets-usp-10-mg-batch-number

Getinge / Atrium Medical Corporation Issues Medical Device Correction for Nurse Assist Syringes Provided with Express Drains | FDA

...notified affected customers of a nationwide recall (medical device correction) for...response to a voluntary medical device recall initiated by a supplier, Nurse Assist...Drains When a company announces a recall, market withdrawal, or safety alert...Announcement View Product Photos More Recalls, Market Withdrawals, & Safety Alerts
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/getinge-atrium-medical-corporation-issues-medical-device-correction-nurse-assist-syringes-provided

Fresenius Kabi Issues Voluntary Nationwide Recall of Two Lots of Dexmedetomidine Hydrochloride Injection Due to Cross-Contamination of Lidocaine | FDA

This recall has been completed and FDA has terminated this recall....Fresenius Kabi Issues Voluntary Nationwide Recall of Two Lots of Dexmedetomidine...Lidocaine 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-two-lots-dexmedetomidine-hydrochloride-injection

Scenic Fruit Company Recalls Organic Pineapple Because of Possible Health Risk | FDA

This recall has been completed and FDA has terminated this recall....Company Recalls Organic Pineapple Because of Possible Health Risk This recall has...has terminated this recall. When a company announces a recall, market withdrawal
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/scenic-fruit-company-recalls-organic-pineapple-because-possible-health-risk

Buzzagogo, Inc. Issues Voluntary Nationwide Recall of Allergy Bee Gone for Kids Nasal Swab Remedy Due to Potential Microbial Contamination | FDA

This recall has been completed and FDA has terminated this recall....Buzzagogo, Inc. Issues Voluntary Nationwide Recall of Allergy Bee Gone for Kids...Contamination This recall has been completed and FDA has terminated this recall. When a
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/buzzagogo-inc-issues-voluntary-nationwide-recall-allergy-bee-gone-kids-nasal-swab-remedy-due

Reckitt/Mead Johnson Nutrition Voluntarily Recalls Select Batches of Nutramigen Hypoallergenic Infant Formula Powder Because of Possible Health Risk | FDA

This recall has been completed and FDA has terminated this recall....Reckitt/Mead Johnson Nutrition Voluntarily Recalls Select Batches of Nutramigen Hypoallergenic...Risk This recall has been completed and FDA has terminated this recall. When a
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/reckittmead-johnson-nutrition-voluntarily-recalls-select-batches-nutramigen-hypoallergenic-infant

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

Gear Isle Issues Voluntary Nationwide Recall of Pro Power Knight Plus, NUX Male Enhancement and DYNAMITE SUPER Capsules Due to the Presence of Sildenafil and Tadalafil | FDA

Sacramento, CA, Gear Isle is voluntarily recalling the following products listed in...ANNOUNCEMENT Gear Isle Issues Voluntary Nationwide Recall of Pro Power Knight Plus, NUX...Tadalafil When a company announces a recall, market withdrawal, or safety alert
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/gear-isle-issues-voluntary-nationwide-recall-pro-power-knight-plus-nux-male-enhancement-and-dynamite