Recalls

All US Product Recalls

Searchable archive of product recalls from the FDA, USDA FSIS, CPSC, NHTSA, and EPA — translated into plain English, severity-scored from objective criteria, and always linked back to the original government notice.

Agency

All agencies FDA (Food)FDA (Drugs)FDA (Devices)USDA FSIS CPSC NHTSA EPA

501–525 of 26077

HighFDA (Food)·H-0797-2026·2026-05-27
Liposomal Womens 50+ Multivitamin Drops recalled due to bacterial contamination risk
Wellnov Supplements is recalling 474 bottles of Liposomal Womens 50+ Liquid Multivitamin Drops due to manufacturing deviations that could allow bacterial contamination, including possible Clostridium botulinum.
Product
Liposomal Womens 50+ Liquid Multivitamin Drops. Dosage: 3ml Liquid. Packaging: Aluminum bottle. 90 ml. Firm Address: Vitaminally LLC Chandler, AZ 85225.
Category
Food
Distribution
Distributed nationwide
HighUSDA FSIS·PHA-05242026-01·2026-05-24
Beef Kofta Products from The Kebab Shop Due to E. Coli Contamination
The USDA Food Safety and Inspection Service issued a public health alert for beef kofta served at The Kebab Shop restaurant locations in California, Texas, and Florida due to possible E. coli O157:H7 contamination. Nine people in California have become ill.
Product
Olympia Food Industries, Inc. — FSIS Issues Public Health Alert for Beef Kofta Products Served at The Kebab Shop Restaurant Locations Due to Possible E. Coli O157:H7 Contamination
Category
Food
Distribution
3 states
SevereCPSC·26503·2026-05-21
WSDZ Light-up Shot Glasses Recalled Due to Button Battery Ingestion Risk
ABC Trading is recalling WSDZ Light-up Shot Glasses because the button cell batteries can be easily accessed by children, creating an ingestion hazard that can cause serious internal injuries or death. No injuries have been reported.
Product
WSDZ Light-up Shot Glasses
Category
Consumer Product
Distribution
Distributed nationwide
SevereCPSC·26501·2026-05-21
Sierra 125U Youth All-Terrain Vehicles Recalled for Crash and Burn Hazards
Lil Pick Up Inc. has recalled about 700 Sierra 125U Youth ATVs sold from October 2025 through April 2026 due to defects that violate federal safety standards and pose risks of serious injury or death, including suspension failures, faulty reverse lights, failing brakes, and hot surfaces.
Product
Sierra 125U Youth All-Terrain Vehicles (ATVs)
Category
Vehicle
Distribution
Distributed nationwide
SevereCPSC·26504·2026-05-21
Bethlehem Lights 10-inch Illuminated Ribbon Spheres Recalled for Fire Hazard
Bethlehem Lights 10-inch Illuminated Ribbon Spheres are recalled because the LED lights can overheat and spark, posing a risk of serious injury or death from fire. About 2,000 units sold online through QVC from July 2024 to April 2026 are affected.
Product
Bethlehem Lights 10-inch Illuminated Ribbon Spheres
Category
Consumer Product
Distribution
Distributed nationwide
SevereCPSC·26502·2026-05-21
Portable Hook-On Chairs Recalled Due to Fall Hazard Risk
PandaEar is recalling about 9,700 portable hook-on chairs sold online because the crotch restraints can be removed without tools, allowing infants to fall through openings. No injuries have been reported.
Product
Portable Hook-On Chairs
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·26499·2026-05-21
Orb Funkee Squeeze Toys Recalled Due to Asbestos Exposure Risk
The Orb Factory is recalling approximately 121,340 Orb Funkee squeeze toys (model 17451 and 41929) because the sand filling may contain fibrous tremolite asbestos. No illnesses have been reported, but inhalation of the asbestos fibers poses a serious health risk.
Product
Orb Funkee Squeeze Toys
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·26498·2026-05-21
HomeProGym Resistance Bands Recalled Due to Impact Hazard
HomeProGym is recalling certain purple 60-pound and gray 70-pound resistance bands because they can forcefully separate from the handle during use, posing a risk of serious injury. Five reports of separation have been received with no injuries reported.
Product
HomeProGym Resistance Bands
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·26497·2026-05-21
Children's Toys with Accessible Button Batteries Recalled for Ingestion Risk
ABC Trading recalls toy headbands and electronic pet cages because button cell batteries are easily accessible to children, posing a risk of serious injury or death if swallowed. About 84,700 units sold nationwide from November 2022 through October 2025 are affected.
Product
Toy Headbands, Electronic Pet Cage-Dinosaur Tribes, My Pet Bird Cute Bird Tribes
Category
Consumer Product
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2159-2026·2026-05-20
NextStep Hemodialysis Catheters with Defective Sheath Introducer
Arrow International is recalling NextStep Antegrade and Retrograde Hemodialysis Catheters worldwide because an included 16F dual-valved splittable sheath introducer may not split as intended, potentially causing pain, bleeding, hematoma, and tissue injury.
Product
NextStep Antegrade Chronic Hemodialysis Catheter, REF: AC-15192-SFX, AC-15232-SFX, CS-15192-SFX, CS-15232-SFX, CS-15272-SFX, CS-15312-SFX, CS-15422-SFX, CS-15502-SFX; NextStep Antegrade Hemodialysis Catheter with Arrow Simplicity Micro-Introducer, REF: CS-15192-SFXM, CS-1523
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2144-2026·2026-05-20
Medline Cardiac Catheterization Kits Recalled for Particulate Contamination
Medline Industries is recalling multiple cardiac catheterization kits due to the presence of particulate matter in the fluid path of manifolds. The affected kits were distributed nationwide and internationally.
Product
1. DBD-MTS,3V,MAN,KIT, Medline Kit Number/SKU 60010195; 2. MTS-LEFT HEART,KIT, Medline Kit Number/SKU 60033123; 3. MTS,3 VALVE,KIT, Medline Kit Number/SKU 60050183; 4. MTS,LEFT HEART,KIT, Medline Kit Number/SKU 60080349; 5. MTS,3 VALVE,LEFT HEART,KIT, Medline Kit Number/S
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2145-2026·2026-05-20
Medline Cardiac Catheterization Kits Recalled for Particulate Contamination
Medline Industries is recalling multiple cardiac catheterization kits because particulate contamination has been found within the fluid path of the manifolds used in these kits.
Product
1. 3 VALVE MAN KIT, Medline Kit SKU Number: 65101544; 2. 3V MANIFOLD KIT, Medline Kit SKU Number: 65110351; 3. HEART CATH PACK-LF, Medline Kit SKU Number: DYNJ0373285M; 4. ANGIO DRAPE CARDIAC PACK, Medline Kit SKU Number: DYNJ51615P; 5. ANGIO DRAPE CARDIAC PACK, Medli
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0525-2026·2026-05-20
Oasis Tears PF Lubricant Eye Drops Recalled for Sterility Assurance
Oasis Medical, Inc. is recalling Oasis Tears PF preservative-free lubricant eye drops nationwide due to lack of assurance of sterility following FDA observations during an inspection.
Product
OASIS TEARS PF — OASIS TEARS PF (GLYCERIN)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2200-2026·2026-05-20
LVIS Intraluminal Support Device Stent Recalled Dimensional Nonconformance
MICROVENTION INC. is recalling LVIS Intraluminal Support Devices due to dimensional nonconformance and incorrect device configuration that may result from manufacturing commingling, creating risk of vessel injury, thrombosis, or neurological events.
Product
LVIS Intraluminal Support Device, REF/Outside Diameter(OD)xTotal Length(TL)xWorking Length(WL): 214022-CAS/4.0 mm x 22 mm x 18 mm, 214518-CAS/4.5 mm x 18 mm x 14 mm, 213517-CAS/3.5 mm x 17 mm x 13 mm
Category
Medical Device
Distribution
0 states
SevereFDA (Food)·H-0853-2026·2026-05-20
Organic Peppermint Leaf Powder Recalled for Potential Salmonella Contamination
Pure Ground Ingredients is recalling Organic Peppermint Leaf Powder due to potential Salmonella contamination. The affected product was distributed in California.
Product
Pure Ground Ingredients-Organic Peppermint Leaf Powder. wholesale bulk; tea/food manufacturers. Closed container stored in a cool settings at ambient/room temperature, free of direct sunlight. Packaging: Box with poly liner. Net wt: total produced 581 lbs. Firm Name/Address: Pure
Category
Food
Distribution
1 state
SevereFDA (Devices)·Z-2047-2026·2026-05-20
Omnicell i.v.Station label stock rolls for syringe preparation
Omnicell is recalling rolls of label stock used in the i.v.Station automation device due to potential for mislabeled syringes during IV medication preparation and compounding.
Product
Rolls of label stock used with the Omnicell i.v.Station. 1. Part Number 258920028, LABEL, STERILE, IVSTATION SYRINGE (40MMX40MM). 2. Part Number 258900029, LABEL, STERILE, IVSTATION SYRINGE (20MMX40MM). Model/Catalog Number: IVS-RBT-001. i.v.STATION is an automat
Category
Medical Device
Distribution
0 states
SevereFDA (Devices)·Z-2186-2026·2026-05-20
Reprocessed Electrophysiology Catheters Recalled for Incomplete Seals
Stryker Sustainability Solutions is recalling Daig Livewire Steerable reprocessed electrophysiology catheters due to incomplete seals on sterile product packaging, which could compromise sterility and patient safety.
Product
Daig Livewire Steerable, Product Number 401575; REPROCESSED ELECTROPHYSIOLOGY CATHETER
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2158-2026·2026-05-20
Cannon II Plus Hemodialysis Catheter Recall Due to Sheath Introducer Defect
Arrow International is recalling Cannon II Plus Hemodialysis Catheters due to a defective sheath introducer that may not split properly, potentially causing withdrawal resistance, prolonged procedure time, pain, bleeding, hematoma, and tissue injury.
Product
Cannon II Plus Hemodialysis Catheter, REF: CS-15242-VSP, CS-15282-VSP, CS-15322-VSP, CS-15362-VSP, CS-15552-VSP, CSD-15242-SP, CSD-15282-SP; Cannon II Plus Hemodialysis Catheter with Arrow Simplicity Micro-Introducer, REF: CS-15242-SPM, CS-15282-SPM, CS-15322-SPM, CS-15362-SPM
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2139-2026·2026-05-20
Namic Angiographic Manifold recalls due to particulate contamination
Medline Industries is recalling Namic Angiographic Manifolds because particulate has been found in the fluid path of the devices. The affected units were distributed nationwide in the U.S. and internationally.
Product
Namic Angiographic Manifold, custom, Medline Product Number/SKU 64038301; Cardiopulmonary bypass adaptor, stopcock, manifold, or fitting.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·H-0781-2026·2026-05-20
Kroger Cheese and Garlic Croutons recalled for possible salmonella contamination
Kroger HOMESTYLE Cheese and Garlic Croutons are being recalled due to possible salmonella contamination in the non-fat milk powder ingredient. The product was distributed to retailers in Indiana, Tennessee, and Wisconsin.
Product
Kroger HOMESTYLE Cheese AND Garlic CROUTONS NET WT 5 OZ (141g) UPC 0 11110 81353 4 DISTRIBUTED BY THE KROGER CO., CINCINNATI, OHIO 45202
Category
Food
Distribution
3 states
SevereFDA (Devices)·Z-2138-2026·2026-05-20
Namic Angiographic Manifold Recalled for Particulate Contamination
Medline Industries is recalling approximately 7,075 units of the Namic Angiographic Manifold (SKU 64038200) due to particulate found in the fluid path. The manifold is used in cardiopulmonary bypass procedures and is distributed across the US and internationally.
Product
Namic Angiographic Manifold, custom, Medline Product Number/SKU 64038200; Cardiopulmonary bypass adaptor, stopcock, manifold, or fitting.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2142-2026·2026-05-20
Namic Preceptor Manifold extravascular blood pressure transducer
Medline is recalling the Namic Preceptor Manifold due to particulate matter found in the fluid path. The recall affects 760 units distributed in the US and eight other countries.
Product
Namic Preceptor Manifold, custom, Medline Product Number/SKU 64039307; Extravascular blood pressure transducer
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2066-2026·2026-05-20
Medical Angiographic Control Syringes Recalled for Rotating Adapter Risk
Windstone Medical Packaging is recalling Custom Convenience Kits containing Medline Namic Angiographic Control Syringes due to risk that the rotating adapter may unwind during use, potentially causing disconnection and exposure to biohazards, blood loss, infection, or air embolism.
Product
Custom Convenience Kit containing recalled Medline Namic Angiographic Control Syringes with Rotating Adapter (Namic RA Syringes) Angio Pack Part numbers AMS6908E, AMS6908F
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2146-2026·2026-05-20
Medline Medical Convenience Kits with Namic Manifold Fluid Contamination
Medline Industries is recalling medical convenience kits (HEART CATH PACK-LF, Kit Number DYNJ36478B) due to particulate matter found in the fluid path of the Namic Manifold. Affected kits were distributed in the US and internationally.
Product
Medline medical convenience kits, containing Namic Manifold, Labeled as: HEART CATH PACK-LF, Medline Kit Number/SKU DYNJ36478B
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2167-2026·2026-05-20
Hologic Selenia Dimensions Mammography Systems Loose Internal Bolts
Hologic has recalled Selenia Dimensions Mammography Systems because internal bolts may become loose, missing, or broken over time. The company has received complaints of this issue affecting systems nationwide.
Product
SELENIA DIMENSIONS MAMMOGRAPHY SYSTEMS. Model Numbers: SDA-SYS-3000-2D-HTC, SDA-SYS-3000-3D, SDM-SYS-6000-2D, SDM-SYS-6000-3D, SDM-00001-2D, SDM-00001-3D, SDM-00001-M2D, SDM-00001-M3D, SDM-05000-2A2, SDM-05000-2A3, SDM-05000-2AC, SDM-05000-2D2, SDM-05000-2D3, SDM-05000-2DC, SDM-0
Category
Medical Device
Distribution
Distributed nationwide

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