🔔 Product Recalls & Refunds

Product recalls offering refunds, replacements, or repairs to consumers who purchased the item. Browse 4,751 active opportunities below.

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When the FDA, CPSC, NHTSA, or another regulatory agency determines a product is unsafe or defective, manufacturers are required to issue a recall. Consumers who purchased the recalled item are typically entitled to a full refund, free replacement, or free repair — at no cost to them. Over 3,000 active FDA recalls are currently tracked in our database, covering food products, prescription drugs, over-the-counter medications, medical devices, and consumer electronics. CPSC recalls cover children's toys, furniture, appliances, and sporting goods. Claiming a recall remedy is usually quick — most require only contacting the manufacturer or returning the product to the retailer.

Product Recalls & Refunds (4,751 active — showing top 30 of 4,751)

Warren James Recalls the Copper Cup Found in Flashgitz Relic Lunch Boxes Due to Risk of Serious Injury or Death from Lead Poisoning Free replacement available

This recall involves the copper cup found in the Flashgitz-branded Space King No Girls Allowed Relic Lunch Boxes. The Relic Box is a retro style lunch box conta…

Product Recall National

Wade Logan Annyka 9-Drawer Fabric Dressers Recalled Due to Risk of Serious Injury or Death from Tip-Over and Entrapment Hazards; Violate Mandatory Standard for Clothing Storage Units; Imported by Nin… Full refund available

This recall involves Wade Logan Annyka 9-Drawer Fabric Dressers. The recalled dressers are made of fabric and a metal frame, and were sold in black, brown, gray…

Product Recall National

TOMY Recalls Boon PIVOT Collapsible Toddler Tower Kitchen Step Stools Due to Risk of Serious Injury and Death from Tip-Over and Fall Hazards Free repair available

This recall involves Boon PIVOT Toddler Tower Kids Kitchen Step Stools. The metal and plastic tower stools were sold in gray and white and measure about 22 inch…

Product Recall National

Target Recalls Cat & Jack Children's Sandals Due to Risk of Serious Injury or Death from Choking Hazard Full refund available

This recall involves Cat & Jack-branded children's sandals. The sandals are tan and have two raffia straps with gold buckles and plastic pearls. The brand is pr…

Product Recall National

SDADI Kitchen Step Stools Recalled Due to Risk of Serious Injury and Death from Entrapment and Fall Hazards; Imported by Yiwushi Bihe Trading Full refund available

SDADI Kitchen Step Stools are wooden standing towers for kids. The towers were sold under model numbers LT05 and LT01 in gray, white, espresso, pink and natural…

Product Recall National

Panasonic Recalls Electric Toaster Ovens Due to Shock and Fire Hazards Full refund available

This recall involves all Panasonic Electric Toaster Ovens, Model No. NB-G200. The Electric Toaster Ovens are stainless steel with the temperature knob located o…

Product Recall National

Oitnlaughter Projecting Finger Light Toys Recalled Due to Risk of Serious Injury or Death from Battery Ingestion; Violate Mandatory Standard for Toys; Sold on Amazon by Delightmi Full refund available

This recall involves Oitnlaughter-branded LED Finger Lights. They were sold in sets of 36 multi-colored lights. Each finger light has three internal button cell…

Product Recall National

Noerishia Adult Portable Bed Rails Recalled Due to Risk of Serious Injury or Death from Entrapment and Asphyxiation; Violates Mandatory Standard for Adult Portable Bed Rails; Sold on Amazon by Hurzein Refund available

This recall involves Noerishia adult portable bed rails. The bed rails come in black, measure 24 inches wide by 36 inches tall, are made of carbon steel, and we…

Product Recall National

MNIENT Adult Portable Bed Rails Recalled Due to Risk of Serious Injury or Death from Entrapment and Asphyxiation; Violate Mandatory Standard for Adult Portable Bed Rails Full refund available

This recall involves MNIENT-branded adult portable bed rails, model LQX-110055. The recalled bed rails have a white frame with black foam rubber handle grips, a…

Product Recall National

Madewell Recalls Women's Sweaters Due to Due to Risk of Serious Injury or Death from Burn Hazard; Violate Mandatory Standard for Clothing Textiles Full refund available

This recall involves two styles of Madewell-branded Double V-Neck Pullover and V-Neck Cardigan women's sweaters. The sweaters were sold with or without buttons

Product Recall National

Liizousuda Paint Thinner Bottles Recalled Due to Risk of Serious Injury or Death from Child Poisoning; Violate Mandatory Standard for Child-Resistant Packaging; Sold on Amazon.com by Shenzhen Gudebo… Free replacement available

This recall involves Liizousuda paint thinner bottles. The paint thinner comes in a clear bottle with a black cap and a wraparound label. The label states "Odor…

Product Recall National

Jobon Torch Lighters Recalled Due to Risk of Serious Injury or Death from Fire and Burn Hazards; Violate Mandatory Standard for Multipurpose Lighters Full refund available

This recall involves Jobon butane torch lighters. The lighters have a side ignition trigger and hands-free operation lock. The lighters come in gray/brown, gold…

Product Recall National

Huish Outdoors Recalls Hollis Diving Regulators Due to Risk of Serious Injury or Death from Drowning Free repair available

This recall involves Hollis 200LX second stage diving regulators. The regulators are used for Scuba diving and are made of black and red plastic and metal. "200…

Product Recall National

Currey & Company Recalls Nottaway Chandeliers Due to Risk of Serious Injury or Death from Electrocution Hazard Free replacement available

This recall involves Currey & Company's Nottaway chandeliers. The iron with brass frame light fixtures were sold in gold, bronze and champagne finishes and in t…

Product Recall National

Boehringer Ingelheim Pharmaceuticals, Inc.: Synjardy XR Tablets (empagliflozin and metformin hydrochloride extended-release tablets), 12.5/1000 mg, 60 Tablets per Bottle, Rx only, Distributed by: Boehringer Ingelheim Pharmaceuticals, Inc., Ridgefield FDA drug recall — return recalled medication to your pharmacy for a full refund of purchase price

Recall reason: CGMP Deviations: An incorrect detergent was used and the required swab sampling was not performed on a production hopper that had previously been…

Product Recall CT

Lannett Company Inc.: Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate and Amphetamine Sulfate Extended-Release Capsules, 5 mg, Rx Only, 100 capsules, Distributed by: Lannett Company, Inc., Philadelphia, PA 1 FDA drug recall — return recalled medication to your pharmacy for a full refund of purchase price

Recall reason: Labeling: Label Mix-up: Capsules contain only immediate-release (IR) pellets while labeled as ER capsules.. Recalled by Lannett Company Inc.. Dis…

Product Recall National

CareFusion 213, LLC: BD ChloraPrep Clear, (2% w/v chlorhexidine gluconate (CHG), and 70% v/v isopropyl alcohol (IPA), Packaged as a) 100 x 3ml applicators/case, NDC 54365-400-32, catalog 930400NS; b) 250 x 3ml applicators/case, NDC 54365-400-32, bulk FDA drug recall — return recalled medication to your pharmacy for a full refund of purchase price

Recall reason: Lack of assurance of sterility: Unsterilized ChloraPrep & PurPrep Applicators, intended for further processing and sterilization were instead dis…

Product Recall National

CareFusion 213, LLC: BD ChloraPrep Hi-Lite Orange, (2% w/v chlorhexidine gluconate (CHG) and 70% v/v isopropyl alcohol) packaged as: a) 25 x 26 mL applicators/case, NDC 54365-400-38, calatog number 930815NS: b) 50 x 26 mL appliactors/case, bulk catal FDA drug recall — return recalled medication to your pharmacy for a full refund of purchase price

Recall reason: Lack of assurance of sterility: Unsterilized ChloraPrep & PurPrep Applicators, intended for further processing and sterilization were instead dis…

Product Recall National

CareFusion 213, LLC: BD ChloraPrep Scrub Teal, (2% w/v chlorhexidine gluconate (CHG) and 70% v/v isopropyl alcohol) packaged as a) 100 x 10.5 mL Applicators/case, NDC 54365-400-36, catalog number 930725NS; b) 100 x 10.5 mL Applicators/case, bulk cata FDA drug recall — return recalled medication to your pharmacy for a full refund of purchase price

Recall reason: Lack of assurance of sterility: Unsterilized ChloraPrep & PurPrep Applicators, intended for further processing and sterilization were instead dis…

Product Recall National

CareFusion 213, LLC: BD ChloraPrep Hi-Lite Orange, (2% w/v chlorhexidine gluconate (CHG) and 70% v/v isopropyl alcohol) packaged as a) 100 x 3 mL applicators/case, NDC 54365-400-33, calatog 930415NS: b) 250 x 3mL applicators/case, bulk catalog number FDA drug recall — return recalled medication to your pharmacy for a full refund of purchase price

Recall reason: Lack of assurance of sterility: Unsterilized ChloraPrep & PurPrep Applicators, intended for further processing and sterilization were instead dis…

Product Recall National

ACCORD BIOPHARMA INC: IMULDOSA, (ustekinumab-srlf) Injection, 130 mg/26 mL (5mg/mL), Rx only, Single dose vial, Manufactured by Accord BioPharma Inc., 8041 Arco corporate Drive, Suite 200, Raleigh, NC 27617, USA, Manufactured at: Catalent Indiana, LL FDA drug recall — return recalled medication to your pharmacy for a full refund of purchase price

Recall reason: Lack of assurance of Sterility:. Recalled by ACCORD BIOPHARMA INC. Distribution: US Nationwide.. Classification (Class II — potential health risk…

Product Recall National

Asclemed USA Inc.: Lidocaine HCl Injection USP, 1% (10 mg/mL), 5 mL single dose ampule, Rx Only, Distributed by Enovachem Pharmaceuticals, Torrance, CA 90501, NDC: 85766-187-01. FDA drug recall — return recalled medication to your pharmacy for a full refund of purchase price

Recall reason: Lack of Assurance of Sterility. Recalled by Asclemed USA Inc.. Distribution: USA Nationwide. Classification (Class II — potential health risk).

Product Recall National

Cipla USA, Inc.: Cinacalcet Hydrochloride Tablets, 60 mg, 30-count bottle, Rx Only, Manufactured by: Cipla Ltd., MIDC, Patalganga, India; Manufactured for: Cipla USA, Inc., 10 Independence Boulevard, Suite 300, Warren, NJ 07059, NDC 69097-411-02 FDA drug recall — return recalled medication to your pharmacy for a full refund of purchase price

Recall reason: cGMP Deviations: presence of N-nitroso-cinacalcet, above the acceptable daily intake (ADI).. Recalled by Cipla USA, Inc.. Distribution: USA Natio…

Product Recall National

Cipla USA, Inc.: Cinacalcet Hydrochloride Tablets, 90 mg, 30-count bottle, Rx Only, Manufactured by: Cipla Ltd., MIDC, Patalganga, India; Manufactured for: Cipla USA, Inc., 10 Independence Boulevard, Suite 300, Warren, NJ 07059, NDC 69097-412-02 FDA drug recall — return recalled medication to your pharmacy for a full refund of purchase price

Recall reason: cGMP Deviations: presence of N-nitroso-cinacalcet, above the acceptable daily intake (ADI).. Recalled by Cipla USA, Inc.. Distribution: USA Natio…

Product Recall National

CareFusion 213, LLC: BD PurPrep, (Povidone-iodine 8.3% w/w (0.83% available iodine) with isopropyl alcohol 72.5% w/w), 50 x 26 mL Applicator/case, STERILE SOLUTION, CAREFUSION 213, LLC, EL PASO, TX 79912, subsidiary of Beckton, Dickson and Co, Catalo FDA drug recall — return recalled medication to your pharmacy for a full refund of purchase price

Recall reason: Lack of assurance of sterility: Unsterilized ChloraPrep & PurPrep Applicators, intended for further processing and sterilization were instead dis…

Product Recall National

ACCORD HEALTHCARE, INC.: Levothyroxine Sodium Tablets, USP, 300 mcg (0.3mg), 90 Tablets bottles, Rx only, Manufactured for: Accord Healthcare, Inc., Raleigh, NC 27617, Manufactured by: lntas Pharmaceuticals Limited, Camp Road, Selaqui, Dehradun-248 1 FDA drug recall — return recalled medication to your pharmacy for a full refund of purchase price

Recall reason: Subpotent Drug. Recalled by ACCORD HEALTHCARE, INC.. Distribution: US Nationwide.. Classification (Class II — potential health risk). Affected l…

Product Recall National

CareFusion 213, LLC: BD ChloraPrep Scrub Teal, (2% w/v chlorhexidine gluconate (CHG) and 70% v/v isopropyl alcohol) packaged as a) 25 x 26 mL applicators/case, NDC 54365-400-39, catalog number 930825NS, b) 50 x 26 mL applicators/case, NDC 54365-400-3 FDA drug recall — return recalled medication to your pharmacy for a full refund of purchase price

Recall reason: Lack of assurance of sterility: Unsterilized ChloraPrep & PurPrep Applicators, intended for further processing and sterilization were instead dis…

Product Recall National

Lupin Pharmaceuticals Inc.: prednisoLONE Acetate Ophthalmic Suspension, USP, 1%, Rx only, Sterile, a) 5 mL (NDC 70748-332-02); b) 10 mL (NDC 70748-332-03), c) 15 mL (70748-332-04), Manufactured by: Lupin Limited, Pithampur (M.P) 454 775, INDIA FDA drug recall — return recalled medication to your pharmacy for a full refund of purchase price

Recall reason: Presence of Foreign Substance. Recalled by Lupin Pharmaceuticals Inc.. Distribution: U.S. Nationwide. Classification (Class II — potential health…

Product Recall National

CareFusion 213, LLC: BD ChloraPrep CLear, (2% w/v chlorhexidine gluconate (CHG) and 70% v/v isopropyl alcohol),500 x 1 mL applicators/case, STERILE SOLUTION, CareFusion 123, LLC, El Paso, TX, subsidiary of Beckton, Dickson and Co. NDC 54365-400-31, b FDA drug recall — return recalled medication to your pharmacy for a full refund of purchase price

Recall reason: Lack of assurance of sterility: Unsterilized ChloraPrep & PurPrep Applicators, intended for further processing and sterilization were instead dis…

Product Recall National

CareFusion 213, LLC: BD ChloraPrep CLear, (2% w/v chlorhexidine gluconate (CHG) and 70% v/v isopropyl alcohol) 100 x 10.5 mL Applicators/case, STERILE SOLUTION, CareFusion 123, LLC, El Paso, TX, subsidiary of Beckton, Dickson and Co. NDC 54365-400-34 FDA drug recall — return recalled medication to your pharmacy for a full refund of purchase price

Recall reason: Lack of assurance of sterility: Unsterilized ChloraPrep & PurPrep Applicators, intended for further processing and sterilization were instead dis…

Product Recall National

How to claim a product recall refund or replacement

Check if a product you own has been recalled. Search our database by product type, brand, or keyword. You can also check recalls.gov for the official CPSC and multi-agency recall database.
Read the recall notice carefully. It will specify what the issue is, which product lots or date codes are affected, and exactly what remedy (refund, replacement, or repair) is being offered.
Stop using the recalled product immediately, especially for food, drug, or safety-critical recalls.
Follow the remedy instructions. For food recalls, discard the product or return it to the store for a refund. For device and product recalls, contact the manufacturer using the information in the recall notice.
Keep your original receipt if you have it, but most recalls do not require proof of purchase — the product's lot number or serial number is usually sufficient.
Document your claim. Note the date you contacted the manufacturer, the representative's name, and any confirmation numbers provided.

Frequently Asked Questions

How do I find out if a product I own has been recalled?+

Search our database by brand or product name. You can also check recalls.gov (CPSC), fda.gov/safety/recalls-market-withdrawals-safety-alerts (FDA), or nhtsa.gov/vehicle-safety/recalls (NHTSA). Sign up for recall alerts from the relevant agency to be notified automatically.

Do I need a receipt to claim a product recall?+

Usually not. Most recalls identify affected products by lot number, date code, or serial number on the package or product itself. Manufacturers cannot require proof of purchase for safety recalls. Check the specific recall notice for any documentation requirements.

How long do I have to claim a recall remedy?+

Recall remedies typically remain available for at least one year, and many remain open indefinitely for safety-critical recalls. However, funds are sometimes limited, so it is best to act promptly. Our database shows the current status of each recall — we remove recalls once they close.

What is the difference between a Class I, II, and III FDA recall?+

Class I recalls involve products with a reasonable probability of causing serious health consequences or death (e.g., contaminated food, incorrect drug strength). Class II recalls involve products that may cause temporary or medically reversible health problems. Class III recalls involve products unlikely to cause any health consequences but that violate FDA regulations.

Can I get a refund for a recalled prescription drug?+

Yes. For recalled prescription medications, return the unused portion to the pharmacy where you purchased it. The pharmacy is required to accept returned recalled medications and provide a refund or work with your insurance to reverse the claim. Contact the manufacturer's recall hotline if the pharmacy is unresponsive.

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