Safety Recalls
RSS ↗15,062 recalls across FDA food, drug, and medical device recalls, CPSC consumer products, and NHTSA vehicles.
Showing 151–200 of 15,062
- Class I
Drug Recall · May 28, 2026
BD ChloraPrep Clear (2% w/v chlorhexidine gluconate (CHG) and 70% v/v isopropyl alcohol (IPA)), 1 mL Applicator, 60 Applicators per inner Carton, Sterile Solution, Care Fusion 213, LLC, El Paso, TX 79Non-Sterility: Due to presence of Aspergillus penicillioides.
- Class II
Drug Recall · May 28, 2026
TopCare health, EXTRA STRENGTH, Antacid Tablets, CALCIUM CARBONATE 750mg, 96 CHEWABLE TABLETS, DISTRIBUTED BY TOPCO ASSOCIATES LLC.,ELK GROVE VILLAGE, IL 60007, NDC 76162-128-22.Presence of foreign substance: small metallic particles in chewable tablets.
- Class II
Drug Recall · May 28, 2026
MARKET BASKET ANTACID Calcium Carbonate 1000 mg, ULTRA STRENGTH, 72 Tablets, Distributed by: De Moules Supermarkets, Inc.,Tewksbury, Mass 01875, UPC 0 49705 83149 6.Presence of foreign substance: small metallic particles in chewable tablets.
- Unclassified
Consumer Product Recall · May 28, 2026
Hop Thang Interior Wood Co. Ltd., of Vietnam
Mainstays 9-Drawer Fabric DressersThe recalled dressers are unstable if they are not anchored to the wall, posing tip-over and entrapment hazards that can result in risk of serious injuries or death to children. The dressers violate the mandatory safety standard as required by the STURDY Act.
- Unclassified
Consumer Product Recall · May 28, 2026
Giantex Inc., of Ontario, California
Giantex and Costway 2-liter and 3-liter Portable Steam SaunasThe sauna's steam diffuser can be positioned too close to a consumer's body, allowing hot steam to come in contact with user, posing a burn hazard.
- Unclassified
Consumer Product Recall · May 28, 2026
Zhejiang Mingrui Furniture Co. Ltd. aka Joy Furniture
Talan and Royce Collection Sofas, Loveseats and ReclinersThe power switch on the sofa, loveseat, or recliner can malfunction and overheat posing a risk of serious injury from a fire hazard.
- Class II
Drug Recall · May 28, 2026
24/7 life BY 7-ELEVEN, Extra strength Antacid Tablets, Calcium Carbonate 750 mg, 96 chewable tablets, DISTRIBUTED BY 7-ELEVEN, IRVING, TX 75063, UPC 0 5254863573 2.Presence of foreign substance: small metallic particles in chewable tablets.
- Class II
Drug Recall · May 28, 2026
GOODSENSE Extra Strength, Antacid TABLETS, Calcium Carbonate 750 mg, 96 Chewable Tablets, Distributed by: Geiss, Destin & Dunn, inc., Peachtree City, GA, NDC 50804-129-22.Presence of foreign substance: small metallic particles in chewable tablets.
- Unclassified
Consumer Product Recall · May 28, 2026
Giantex Inc., of Ontario, California
Giantex outdoor lounge chairsConsumers can place their fingers in a pinch point, when adjusting the lounge chair, posing an amputation risk.
- Class II
Drug Recall · May 28, 2026
Good Neighbor Pharmacy, extra strength Antacid Calcium Carbonate 1000 mg, 72 chewable tablets, Distributed by: Amerisourcebergen, 1 West First Avenue, Conshohocken, PA, 19428, NDC 24385-595-23.Presence of foreign substance: small metallic particles in chewable tablets.
- Class II
Drug Recall · May 28, 2026
Harris Teeter, ULTRA STRENGTH ANTACID, Calcium Carbonate 1000 mg, 72 CHEWABLE TABLETS, Distributed by: Harris Teeter, LLC.,MATTHEWS, NC 28105, UPC: 0 72036-73108-1.Presence of foreign substance: small metallic particles in chewable tablets.
- Class II
Drug Recall · May 28, 2026
Good Neighbor Pharmacy, extra strength Antacid Calcium Carbonate 750 mg, chewable, 96-count bottle, Distributed by: Amerisourcebergen, 1 West First Avenue, Conshohocken, PA, 19428, NDC 24385-106-80.Presence of foreign substance: small metallic particles in chewable tablets.
- Class II
Drug Recall · May 28, 2026
BD ChloraPrep FREPP Clear, (2% w/v chlorhexidine gluconate (CHG) and 70% v/v isopropyl alcohol (IPA) 1.5 mL Applicator, 20 Applicators, Sterile Solution, Care Fusion 213, LLC, El Paso, TX 79912, subsLack of Assurance of Sterility: Due to wrinkles in the paper lidding which may breach the seal area.
- Class II
Drug Recall · May 28, 2026
FAMILY WELLNESS, ULTRA STRENGT, ANTACID TABLETS, Calcium Carbonate 1000 mg, 72 CHEWABLE TABLETS, DISTRIBUTED BY: MIDWOOD BRANDS, LLC, 500 VOLVO PKWY, CHESAPEAKE, VA 23320 USA., UP: 0 32251-92282-4.Presence of foreign substance: small metallic particles in chewable tablets.
- Class II
Drug Recall · May 28, 2026
KIRKLAND Signature, ULTRA STRENGTH ANTACID, Calcium Carbonate, 1000 mg, 265-count bottle, MANUFACTURED BY: GUARDIAN DRUG COMPANY, INC., 2 CHARLES COURT/DAYTON, NJ 08810, FOR: Costco Wholesale CorporatPresence of foreign substance: small metallic particles in chewable tablets.
- Class I
Drug Recall · May 28, 2026
BD ChloraPrep FREPP Clear,(2% w/v chlorhexidine gluconate (CHG) and 70% v/v isopropyl alcohol (IPA)) 1.5 mL Applicator, 20 Applicators, Sterile Solution, Care Fusion 213, LLC, El Paso, TX 79912, subsiNon-Sterility: Due to presence of Aspergillus penicillioides. And Lack of Assurance of Sterility: Due to wrinkles in the paper lidding which may breach the seal area.
- Class II
Drug Recall · May 28, 2026
Extra strength Antacid Calcium Carbonate 750 mg, chewable tablets, 96-count bottle, DISTRIBUTED BY CASEY'S MARKETING COMPANY, ANKENY, IA 50521, UPC: 0 98437 24361 9.Presence of foreign substance: small metallic particles in chewable tablets.
- Unclassified
Consumer Product Recall · May 28, 2026
Proudly American Store, of Canada
VL2020 Lithium Coin BatteriesThe recalled coin batteries are not in child-resistant packaging and do not bear the warning labels required under Reese's Law. When button cell or coin batteries are swallowed, the ingested batteries can cause serious injuries, internal chemical burns, and death.
- Class II
Drug Recall · May 28, 2026
GOODSENSE Ultra Strength, Antacid TABLETS, Calcium Carbonate 1000 mg, 72 Chewable Tablets, Distributed by: Geiss, Destin & Dunn, inc., Peachtree City, GA, NDC 50804-171-68.Presence of foreign substance: small metallic particles in chewable tablets.
- Unclassified
Consumer Product Recall · May 28, 2026
Missry Associates, Inc., doing business as Misco Enterprises, of Edison, New Jersey
Misco Sports Light-Up Racket Sets, model MT2287The racket sets violate the mandatory standard for toys because the screw on the racket used to secure the battery compartment does not remain attached when opened, and the button cell batteries in the shuttlecock can be easily accessed by children. If button cell or coin batteries are swallowed, the ingested batteries can cause serious injuries, including internal chemical burns, and death.
- Unclassified
Consumer Product Recall · May 28, 2026
Tzumi Electronics of New York, New York
SLF Sauna BlanketsThe recalled sauna blankets can overheat, posing fire and burn hazards.
- Unclassified
Consumer Product Recall · May 28, 2026
Anzmtosn Luminous Fidget Spinner BallsThe recalled toys violate the?mandatory safety standard for toys?because the mini flashlight included with the fidget spinner balls contains button cell batteries that can be easily accessed by children. If button cell or coin batteries are swallowed, the ingested batteries can cause serious injuries,?including internal chemical burns, and death.
- Class II
Drug Recall · May 28, 2026
HyVee, Ultra Strength Antacid, Calcium Carbonate 1000 mg, 72 CHEWABLE TABLETS, DISTRIBUTED BY: HY-VEE INC., Inc., WEST DES MOINES, IA 50266, UPC: 0 75450 82514 5.Presence of foreign substance: small metallic particles in chewable tablets.
- Class II
Drug Recall · May 28, 2026
CAREone, EXTRA STRENGTH CALCIUM ANTACID, Calcium Carbonate 750 mg, 96 chewable Tablets, Distributed by: FOODHOLD U.S.A, LLC, LANDOVER, MD 20785, NDC 72476-127-80.Presence of foreign substance: small metallic particles in chewable tablets.
- Class II
Drug Recall · May 28, 2026
TopCare health, ULTRA STRENGTH, Antacid Tablets, CALCIUM CARBONATE 1000mg, 72 CHEWABLE TABLETS, DISTRIBUTED BY TOPCO ASSOCIATES LLC.,ELK GROVE VILLAGE, IL 60007, NDC 76162-129-68.Presence of foreign substance: small metallic particles in chewable tablets.
- Class II
Drug Recall · May 28, 2026
HALEON CALCIUM CARBONATE TUMS ANTACID, Assorted Fruit Tablets, 1000 mg, 160-count bottle, Haleon, Warren, NJ 07059, UPC 3 07660 74610 2.Presence of foreign substance: small metallic particles in chewable tablets.
- Class II
Drug Recall · May 27, 2026
Aripiprazole Tablets USP, Rx only, 30 mg, 30 tablets, Marketed by: Ajanta Pharma USA Inc., Bridgewater, NJ 08807, Made in India, NDC 27241-056-03.Product Mix-Up: A bottle containing Voriconazole Tablets 50 mg was labelled and distributed as Aripiprazole Tablets USP 30 mg.
- Class II
Medical Device Recall · May 27, 2026
Advance Aluminum Chloride Gel Clear Hemostatic Gel Kit, Catalog number 504600-28Some units of Aluminum Chloride Gel contain the package insert for Ferric Sulfate Gel. The incorrect insert misidentifies the product and contains different first aid instructions, most critically in that the Ferric Sulfate insert instructs users to induce vomiting in the case of ingestion, while the correct Aluminum Chloride insert instructs users not to induce vomiting.
- Class II
Drug Recall · May 27, 2026
Glenmark Pharmaceuticals Inc., USA
Alyacen 7/7/7, Norethindrone and Ethinyl Estradiol Tablets USP, 0.5mg/0.035mg, 0.75mg/0.035mg, 1 mg/0.0.35mg, 3 Blister Cards each containing 28 tablets, 28 day regimen, Rx only, Manufactured by: GlenFailed Impurities/Degradation Specifications: This recall is being initiated due to out-of-specification results total impurities.
- Class III
Food Recall · May 27, 2026
Roast beef and cheddar closed face sandwich packed in clear plastic wrap with a green adhesive label. The label reads in part as "***Lunch Box Kitchen*** Premium Convenience***Turkey & Cheddar Sub***BIncorrect Product Label; Roast Beef and Swiss closed face sub sandwich labeled as Turkey and Cheddar closed face sub sandwich
- Class II
Medical Device Recall · May 27, 2026
Brand Name: Dexcom G7 Continuous Glucose Monitoring System Product Name: Dexcom G7 US Retail Sensor/Transmitter 1-pack Model/Catalog Number: STP-AT-012 Software Version: N/A Product Description: DCertain lots of Dexcom G7 sensors originally designated as scrap and intended for destruction were stolen during the destruction process. The sensors were later sold to pharmacies and distributors by Pharmsource, LLC. Lot 1725204004 were designated for destruction because the G7 sensors were not properly sterilized and have an increased risk of skin infection if used. Lot 1725069002 were designated for destruction due to an increased risk of having no sensor readings available or experiencing sensor inaccuracy that includes the potential for missed detection of a hyperglycemic event or incorrect treatment decisions that can result in patient injury, including medical intervention to prevent permanent injury or impairment. Additionally, due to the unknown storage and handling and storage conditions these sensors may have undergone during the distribution, these sensors may present additional risk.
- Class II
Drug Recall · May 27, 2026
Niacin Extended-release Tablets, USP, 1,000 mg, 90-count bottles, Rx Only, Distributed by: Lannett Company, Inc., Philadelphia, PA 19136, NDC 62175-322-46.Failed Dissolution Specifications: during 12M LT stability testing OOS low for Stage 3 dissolution at the 24-hour timepoint.
- Class II
Medical Device Recall · May 26, 2026
Philips Avalon Fetal Monitor, FM 30 Part numberM2703AMonitor has incorrect assembly of the speaker connector which can cause device cables to be pulled out of the housing and increase the risk of intermittent or permanent loss of speaker output.
- Class II
Medical Device Recall · May 26, 2026
Philips Avalon Fetal Monitor, FM20, Part number M2702A, Part M2703AMonitor has incorrect assembly of the speaker connector which can cause device cables to be pulled out of the housing and increase the risk of intermittent or permanent loss of speaker output.
- Class II
Drug Recall · May 22, 2026
SUN PHARMACEUTICAL INDUSTRIES INC
Xyvona (levorphanol tartrate tablets), 3mg, 100 Tablets, Rx only, Forte BioPharma, Manufactured by: Ohm Laboratories Inc., New Brunswick, NJ 08901, Distributed by: Fort Bio-Pharma, LLC., Las Vegas, NVLabeling: Not Elsewhere Classified. This recall has been initiated in response to the denial by FDA of marketing the product under the proprietary name Xyvona
- Class II
Food Recall · May 22, 2026
boichik bagles Tuna Salad Ingredients: albacore tuna, mayonnaise (soybean oil, water, whole eggs and egg yolks, distilled vinegar, salt, sugar, lemon juice concentrate, calcium disodium edta, naturalIngredient statement declares eggs, but eggs are omitted from the "contains" allergen statement on the product labels.
- Class I
Medical Device Recall · May 22, 2026
Abiomed 14 Fr x 25 cm Low Profile Introducer Kit for Impella CP. Impella Set Product Code: 1000435. Introducer Product Code: 1000435.Potential for thrombus formation during prolonged use of the introducer.
- Class II
Drug Recall · May 22, 2026
Zep, Alcohol Sanitizer Spray, Ethanol 70%, Net Contents 55 Gallons 208 Liters, Made in USA, A Zep Inc. Brand, Distributed by: Zap Inc., 350 Joe Frank Harris Parkway, SE, Emerson, GA 30137, NDC 66949-1Microbial contamination of sterile products
- Class II
Food Recall · May 22, 2026
boichik bagles Pumpernickel Mix Bagels 6 pre-sliced bagels NET WT 26.5 OZ (1.66 LB) 750g Ingredients: Organic wheat flour ... Contains Wheat Topped flavors may additionally contain ... sesame seedUndeclared allergen, sesame.
- Class I
Medical Device Recall · May 22, 2026
Abiomed 14 Fr x 13 cm Low Profile Introducer Kit for Impella CP. Impella Set Product Code: 1000434. Introducer Product Code: 1000434.Potential for thrombus formation during prolonged use of the introducer.
- Class I
Food Recall · May 22, 2026
1. TNVitamins Ultrapotent Complete Green Superfood Moringa Capsules (120 count) 2. Doctor s Pride Complete Green Superfood Ultra Potent Moringa 10,000 mg (120 capsules)Product may be contaminated with Salmonella.
- Class II
Drug Recall · May 22, 2026
SUN PHARMACEUTICAL INDUSTRIES INC
Xyvona (levorphanol tartrate tablets), 2mg, 100 Tablets, Rx only, Forte BioPharma, Manufactured by: Ohm Laboratories Inc., New Brunswick, NJ 08901, Distributed by: Fort Bio-Pharma, LLC., Las Vegas, NVLabeling: Not Elsewhere Classified. This recall has been initiated in response to the denial by FDA of marketing the product under the proprietary name Xyvona
- Class I
Medical Device Recall · May 22, 2026
Abiomed Impella CP Set with SmartAssist (10th Generation) containing affected 14Fr Low Profile Introducer Kits 13 and 25 cm Japan. Product Code: 1000542.Potential for thrombus formation during prolonged use of the introducer.
- Class II
Food Recall · May 22, 2026
boichik bagels Whitefish Salad Ingredients: Smoked whitefish, mayonnaise (soybean oil, water, whole eggs and egg yolks, distilled vinegar, salt, sugar, lemon juice concentrate, calcium disodium edta,Ingredient statement declares eggs, but eggs are omitted from the "contains" allergen statement on the product labels.
- Class II
Food Recall · May 22, 2026
University of California Health Milk Bank
001165: Standard Pasteurized Donor Human Milk; 100 mL bottles 001198: Pediatric Pasteurized Donor Human Milk; 200 mL bottles No UPCProduct is potentially contaminated with foreign material (plastic particles).
- Class I
Medical Device Recall · May 22, 2026
Abiomed Impella CP Set with SmartAssist (10th Generation) containing affected 14Fr Low Profile Introducer Kits. Product Codes: 1000413, 1000834.Potential for thrombus formation during prolonged use of the introducer.
- Class II
Medical Device Recall · May 21, 2026
BD Connecta" BD Luer-Lok" 360 REF 394910 UDI-DI code: 00382903949106 BD Connecta" Stopcocks are used to administer fluids or medication through one or two different ports via an IV cannula or exteDue to stopcock issues when using the plastic luer-lok syringe, the connection at the Port C may over thread or continue to spin rather than tightening securely. This behavior has led some clinical users to perceive the connection as unstable.
- Class II
Drug Recall · May 21, 2026
safco SensiCaine-Ultra (20% Benzocaine), Topical Anesthetic Gel, Strawberry Flavor, 1 oz. (29.6mL), Distributed by: Safco Dental Supply Co., Buffalo Grove, IL 60099, Made in USA, NDC 67239-0223-1.Defective container:may contain bottles with incomplete seals
- Unclassified
Consumer Product Recall · May 21, 2026
ABC Trading Inc., of Vernon, California
Toy Headbands, Electronic Pet Cage-Dinosaur Tribes, My Pet Bird Cute Bird TribesThe recalled children's toys violate the mandatory standard for toys because they contain button cell batteries and the compartments that hold the batteries can be easily accessed by children, posing a deadly ingestion hazard to children. When button cell and coin batteries are swallowed, the ingested batteries can cause serious injuries, internal chemical burns and death.
- Unclassified
Consumer Product Recall · May 21, 2026
Lil Pick Up Inc., of Rowland Heights, California
Sierra 125U Youth All-Terrain Vehicles (ATVs)The recalled youth ATVs violate the federal mandatory ATV safety standard, posing a risk of serious injury or death. The youth ATVs fail to meet mechanical suspension requirements, and the reverse indicator light fails to illuminate, posing a crash hazard. The parking brakes fail to hold, posing a collision hazard. Additionally, the surfaces near the footwell can reach high temperatures, posing a risk of severe burns.