Safety Recalls

17,395 recalls across FDA food, drug, and medical device recalls, CPSC consumer products, and NHTSA vehicles.

Showing 1,351–1,400 of 17,395

• Drug Recall · May 28, 2026

  Guardian Drug Co. Inc.

  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

• Medical Device Recall · May 28, 2026

  Medline Industries, LP

  Medline Convenience Kits: 1) OPEN HEART PEDS PACK, Model Number: DYNJ88569; 2) OPEN HEART PEDS PACK, Model Number: DYNJ88569A; 3) OPEN HEART PEDS PACK, Model Number: DYNJ88569B; 4) OPEN HEART P

  Convenience Kits contain Covidien Mon-a-Therm General Purpose Temperature Probes Size 9 Fr. Medtronic has issued a recall of specific production lots of the Covidien Mon-a-Therm general purpose temperature probe-size 9 due to an error in its distribution control process.

  Class II

• Drug Recall · May 28, 2026

  Guardian Drug Co. Inc.

  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

  Guardian Drug Co. Inc.

  CAREone, ULTRA STRENGTH CALCIUM ANTACID, Calcium Carbonate 1000 mg, 72 chewable Tablets, Distributed by: FOODHOLD U.S.A, LLC, LANDOVER, MD 20785, NDC 72476-178-23.

  Presence of foreign substance: small metallic particles in chewable tablets.

  Class II

• Drug Recall · May 28, 2026

  Guardian Drug Co. Inc.

  HyVee, Extra Strength Antacid, Calcium Carbonate 750 mg, 96 CHEWABLE TABLETS, DISTRIBUTED BY: HY-VEE INC., Inc., WEST DES MOINES, IA 50266, UPC: 0 75450 82497 1.

  Presence of foreign substance: small metallic particles in chewable tablets.

  Class II

• Consumer Product Recall · May 28, 2026

  Daoen Inc., of City of Industry, California

  Zen Fidget Magnetic Ball Sets

  The recalled magnetic balls violate the mandatory standard for toys because they are loose high-powered magnets, posing an ingestion hazard to children. When high-powered magnets are swallowed, they can attract each other, or other metal objects, and become lodged in the digestive system. This can result in perforations, twisting, and/or blockage of the intestines, blood poisoning and death.

  Unclassified

• Consumer Product Recall · May 28, 2026

  Shenzhenshibangduoladianzikejimaoyi Co., Ltd (Shenzhen Bangduola Electronic Technology Trade Co., Ltd.), doing business as Anzmtosn, of China

  Anzmtosn Luminous Fidget Spinner Balls

  The 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.

  Unclassified

• Drug Recall · May 28, 2026

  Guardian Drug Co. Inc.

  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 28, 2026

  CareFusion 213, LLC

  BD ChloraPrep Clear, (2% w/v chlorhexidine gluconate (CHG) and 70% v/v isopropyl alcohol (IPA) 1 mL Applicator, 60 Applicators, Sterile Solution, Care Fusion 213, LLC, El Paso, TX 79912, subsidiary of

  Lack of Assurance of Sterility: Due to wrinkles in the paper lidding which may breach the seal area.

  Class II

• Medical Device Recall · May 28, 2026

  Medline Industries, LP

  Medline Convenience Kits: 1) OPEN HEART PEDS PACK, Model Number: DYNJ88569D; 2) ACCESSORY KIT, Model Number: DYNJ901348F

  Convenience Kits contain Covidien Mon-a-Therm General Purpose Temperature Probes Size 9 Fr. Medtronic has issued a recall of specific production lots of the Covidien Mon-a-Therm general purpose temperature probe-size 9 due to an error in its distribution control process.

  Class II

• Consumer Product Recall · May 28, 2026

  MiniWarGaming Inc., doing business as MiniWarGaming Forge

  MiniWarGaming and Primal Horizon Disc Magnets

  The magnets violate the mandatory safety standard for magnets because the high-powered magnets fit within CPSC's small parts cylinder and are stronger than permitted, posing a deadly ingestion hazard to children. When high-powered magnets are swallowed, the ingested magnets can attract each other, or other metal objects, and become lodged in the digestive system. This can result in perforations, twisting, and/or blockage of the intestines, blood poisoning and death.

  Unclassified

• Consumer Product Recall · May 28, 2026

  Proudly American Store, of Canada

  VL2020 Lithium Coin Batteries

  The 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.

  Unclassified

• Consumer Product Recall · May 28, 2026

  Giantex Inc., of Ontario, California

  Giantex and Costway 2-liter and 3-liter Portable Steam Saunas

  The 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 Recliners

  The power switch on the sofa, loveseat, or recliner can malfunction and overheat posing a risk of serious injury from a fire hazard.

  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 MT2287

  The 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

• Medical Device Recall · May 28, 2026

  Medline Industries, LP

  Medline Convenience kits containing recalled Swan-Ganz Catheters CENTRAL AND ARTERIAL LINE TOTE DYNJ8407

  Kits contain Swan-Ganz catheters recalled by Becton Dickinson (BD). BD has received complaints of leaks/breakage involving failures of the (blue) proximal injectate lumen hub on these catheters. This has led to instances of leakage, lumen damage, and breakage, and may lead to infection, medication loss, and/or blood loss.

  Class II

• Drug Recall · May 28, 2026

  Guardian Drug Co. Inc.

  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.

  Class II

• Consumer Product Recall · May 28, 2026

  Tzumi Electronics of New York, New York

  SLF Sauna Blankets

  The recalled sauna blankets can overheat, posing fire and burn hazards.

  Unclassified

• Food Recall · May 28, 2026

  Azuma Foods International Inc USA

  azuma foods TAKO WASABI Seasoned Octopus with Wasabi PERISHABLE/KEEP FROZEN PRODUCT OF JAPAN DISTRIBUTED BY: AZUMA FOODS INTERNATIONAL INC., U.S.A. HAYWARD, CA 94545 Retail: 3-50g PACKS NET WT. 5.

  Undeclared fish.

  Class I

• Drug Recall · May 28, 2026

  Guardian Drug Co. Inc.

  H.E.B Extra Strength Calcium Carbonate Antacid Tablets, Calcium Carbonate 750 mg, 96 Chewable Tablets, MADE WITH PRIDE & CARE FOR H.E.B, 646 S. FLORES ST, SAN ANTONIO, TX, NDC 37808-136-22.

  Presence of foreign substance: small metallic particles in chewable tablets.

  Class II

• Drug Recall · May 28, 2026

  Guardian Drug Co. Inc.

  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.

  Class II

• Food Recall · May 28, 2026

  Specialty Bakers, LLC

  Vanilla Dessert Shells (Giant), 6 dessert shells/1 package, 1 dessert shell is approximately 23.67 grams. 1package is 142 grams. 1 package has 1 plastic tray which holds 6 desserts shells. Plastic is

  Undeclared Allergen (Soy)

  Class II

• Consumer Product Recall · May 28, 2026

  Giantex Inc., of Ontario, California

  Giantex outdoor lounge chairs

  Consumers can place their fingers in a pinch point, when adjusting the lounge chair, posing an amputation risk.

  Unclassified

• Consumer Product Recall · May 28, 2026

  Hop Thang Interior Wood Co. Ltd., of Vietnam

  Mainstays 9-Drawer Fabric Dressers

  The 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

• Drug Recall · May 28, 2026

  Guardian Drug Co. Inc.

  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

• Medical Device Recall · May 28, 2026

  Medline Industries, LP

  Medline Convenience kits containing recalled Swan-Ganz Catheters KIT GERMANTOWN CABG DYNJ905855 KIT UNIVERSITY CABG PACK DYNJ905857 OH MED RN CDS DYNJ905936B

  Kits contain Swan-Ganz catheters recalled by Becton Dickinson (BD). BD has received complaints of leaks/breakage involving failures of the (blue) proximal injectate lumen hub on these catheters. This has led to instances of leakage, lumen damage, and breakage, and may lead to infection, medication loss, and/or blood loss.

  Class II

• Drug Recall · May 28, 2026

  Guardian Drug Co. Inc.

  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., NDC 55319-171-68.

  Presence of foreign substance: small metallic particles in chewable tablets.

  Class II

• Medical Device Recall · May 28, 2026

  Medline Industries, LP

  Medline Convenience kits containing recalled Swan-Ganz Catheters CARDIAC MAJOR DYNJ901328G HEART A DYNJ903465K OPEN HEART DYNJ909090G SILVER CROSS OPEN HEART DYNJ906102M

  Kits contain Swan-Ganz catheters recalled by Becton Dickinson (BD). BD has received complaints of leaks/breakage involving failures of the (blue) proximal injectate lumen hub on these catheters. This has led to instances of leakage, lumen damage, and breakage, and may lead to infection, medication loss, and/or blood loss.

  Class II

• Drug Recall · May 28, 2026

  Ajanta Pharma USA Inc

  Fenofibrate Capsules, USP 200 mg, Rx only, 100 Capsules, Manufactured by: Ajanta Pharma Limited, India, Marketed by: Ajanta Pharma USA Inc. Bridgewater, NJ 08807, NDC 27241-120-04.

  CGMP Deviations

  Class II

• Drug Recall · May 28, 2026

  Guardian Drug Co. Inc.

  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

• Food Recall · May 28, 2026

  Wise Foods Inc

  Wise Onion Rings, 3.75 oz, metalized film in cardboard cartons, 14 bags per case,

  The product contains undeclared Yellow 5 and 6, Blue 1, and unapproved Red 3.

  Class II

• Drug Recall · May 28, 2026

  Guardian Drug Co. Inc.

  DISCOUNT drug mart, EXTRA STRENGTH, ANTACID TABLETS, Calcium Carbonate 750 mg, 96 Tablets, Distributed by: Drug Mart- Food Fair Medina, OH 44256, UPC: 0 93351 03992 8.

  Presence of foreign substance: small metallic particles in chewable tablets.

  Class II

• Drug Recall · May 28, 2026

  CareFusion 213, LLC

  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, subsi

  Non-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 I

• Medical Device Recall · May 28, 2026

  Medline Industries, LP

  Medline Convenience kits containing recalled Swan-Ganz Catheters OPEN HEART DYNJ909090B OPEN HEART CDS QVH CDS982523M

  Kits contain Swan-Ganz catheters recalled by Becton Dickinson (BD). BD has received complaints of leaks/breakage involving failures of the (blue) proximal injectate lumen hub on these catheters. This has led to instances of leakage, lumen damage, and breakage, and may lead to infection, medication loss, and/or blood loss.

  Class II

• Drug Recall · May 28, 2026

  CareFusion 213, LLC

  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, subs

  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

  Guardian Drug Co. Inc.

  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

  Guardian Drug Co. Inc.

  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.

  Class II

• Drug Recall · May 28, 2026

  CareFusion 213, LLC

  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 79

  Non-Sterility: Due to presence of Aspergillus penicillioides.

  Class I

• Drug Recall · May 28, 2026

  Guardian Drug Co. Inc.

  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

  Guardian Drug Co. Inc.

  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

  Guardian Drug Co. Inc.

  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

  Guardian Drug Co. Inc.

  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

• Medical Device Recall · May 27, 2026

  Dexcom, Inc.

  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: D

  Certain 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

• Vehicle Recall · May 27, 2026

  Ford Motor Company

  2023 FORD BRONCO SPORT, 2023 FORD MAVERICK, 2024 FORD BRONCO SPORT, 2024 FORD MAVERICK

  A detached control arm can cause a loss of vehicle control, increasing the risk of a crash.

  Unclassified

• Drug Recall · May 27, 2026

  Ajanta Pharma USA Inc

  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

• 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: Glen

  Failed Impurities/Degradation Specifications: This recall is being initiated due to out-of-specification results total impurities.

  Class II

• Vehicle Recall · May 27, 2026

  Toyota Motor Engineering & Manufacturing

  2024 TOYOTA LAND CRUISER HYBRID

  An instrument panel display that fails to show critical safety information, such as engine coolant temperature or electrical charge increases the risk of a crash or injury.

  Unclassified

• Drug Recall · May 27, 2026

  Lannett Company Inc.

  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 27, 2026

  Inter-Med Llc

  Advance Aluminum Chloride Gel Clear Hemostatic Gel Kit, Catalog number 504600-28

  Some 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

• Vehicle Recall · May 27, 2026

  Ford Motor Company

  2025 FORD EXPLORER

  A sudden loss of drive power can increase the risk of a crash.

  Unclassified