Safety Recalls

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17,553 recalls across FDA food, drug, and medical device recalls, CPSC consumer products, and NHTSA vehicles.

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Showing 1,501–1,550 of 17,553

Medical Device Recall · May 28, 2026
Medline Industries, LP
Medline Convenience kits containing recalled Swan-Ganz Catheters CABG A CDS CDS982269K CDS982269L CDS982269M CDS982269N CARDIAC MAJOR DYNJ901328D DYNJ901328F HEART A DYNJ90
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
Medical Device Recall · May 28, 2026
SEASPINE ORTHOPEDICS CORPORATION
SeaSpine Polyaxial Head REF Number: 41-3010
Due to manufacturing error, polyaxial head may popoff from the screw intraoperatively following insertion.
Class II
Drug Recall · May 28, 2026
Guardian Drug Co. Inc.
HALEON CALCIUM CARBONATE TUMS ANTACID, Assorted Fruit Tablets, 750 mg, 330-count bottle, Haleon, Warren, NJ 07059, UPC 3 0766 3072 10 9.
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 RIGHT HEART CATH PACK CTX DYNJ68530B
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.
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.
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, 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
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
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
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
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
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
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
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
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.
EQUALINE extra strength, antacid tablets, calcium carbonate 750mg, 96 chewable tablets, DISTRIBUTED BY SUPERVALU INC.,EDEN PRARIE, MN 55344 USA, NDC 41163-129-22.
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
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
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
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
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
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
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