Safety Recalls
RSS ↗17,395 recalls across FDA food, drug, and medical device recalls, CPSC consumer products, and NHTSA vehicles.
Showing 851–900 of 17,395
- Class III
Drug Recall · July 6, 2026
Supernus Pharmaceuticals, Inc.
Trokendi XR, topiramate extended-release capsules, 25mg, 30 Capsules, Rx only, Manufactured by: Catalent Pharma Solutions, Winchester, KY 40391 USA, Manufactured for: Supernus Pharmaceuticals, Inc., RFailed Dissolution Specifications
- Class II
Drug Recall · July 6, 2026
CLEVIPREX (clevidipine injectable emulsion) 50 mg/100 mL (0.5 mg/mL), 10 Single Use Vials, Rx Only, Manufactured for: Chiesi USA, Inc., Cary, NC 27518, by Fresenius Kabi, Graz, Austria, NDC 10122-611-Lack of Assurance of Sterility
- Class II
Medical Device Recall · July 6, 2026
Siemens Healthcare Diagnostics, Inc.
Atellica CH Urine Albumin REF: 11537225, in vitro diagnosticProcessing of urine albumin assay on the CI analyzers may lead to the following issues: Falsely depressed Atellica CH Urea Nitrogen (UN_c) results; Falsely depressed Atellica CH Enzymatic Hemoglobin A1c (A1c_E) results; Increased rate of reaction cuvette QC failures and Delayed results due to QC failures.
- Class II
Medical Device Recall · July 6, 2026
Esteem Body Soft Convex Urostomy Pouch Model/Catalog Numbers: 423703, 423704, 423705, 423707, 423708, 423709, 423710, 423712, 423713, 423714, 423715, 423716, 423717, 423718, 423721, 423722, 423723, 4Urostomy Pouches may leak from cap during use.
- Class I
Medical Device Recall · July 6, 2026
Brand Name: Elevaris/Spectra Medical Devices Product Name: Sodium Chloride Injection, 0.9%, USP 10mL Ampule Model/Catalog Number: AMPUL10MLK. Sodium Chloride Flush for IV tubing systems and indManufacturing firm, Huons, was cited for issues regarding product quality and sterility assurance. If the product sterility is compromised, patients may be exposed to microorganisms, endotoxins, or foreign matter. This may trigger inflammatory responses, infections, micro-clots, and organ failure.
- Unclassified
Vehicle Recall · July 5, 2026
2026 CADILLAC ESCALADE, 2026 CADILLAC ESCALADE ESV, 2026 CHEVROLET SILVERADO 1500, 2026 CHEVROLET TAHOE, 2026 GMC SIERRA 1500, 2026 GMC YUKON, 2026 GMC YUKON XLFront or rear wheel lockup increases the risk of a crash.
- Class I
Food Recall · July 3, 2026
Frutas y Hortalizas del Sur S.A.
Organic Whole Blueberries, Net Wt 10 oz (284g) plastic bag, packed in 8 bags per case of 10 oz each. Keep FrozenPotential E. coli O145:H28 Contamination
- Unclassified
Vehicle Recall · July 2, 2026
2023 HYUNDAI IONIQ 5, 2024 HYUNDAI IONIQ 5A fire increases the risk of injury.
- Unclassified
Consumer Product Recall · July 2, 2026
Changsha Jiali Duo Technology Co., Ltd., dba Topyond, of China
Topyond Pool Drain Port with CoverThe recalled drain ports with covers violate the entrapment protection standards of the Virginia Graeme Baker Pool and Spa Safety Act (VGBA), posing deadly entrapment and drowning hazards to consumers.
- Unclassified
Vehicle Recall · July 2, 2026
2023 KIA EV6, 2024 KIA EV6, 2024 KIA EV9A fire increases the risk of injury.
- Class II
Drug Recall · July 2, 2026
Mycophenolate Mofetil for Injection USP, 500 mg/Vial, Single Dose Vial, 4 vials per carton, Rx only, Manufactured for: Mylan Institutional LLC, Morgantown, WV, 26505 USA, Made in India, NDC 67457-386-Presence of precipitate
- Unclassified
Consumer Product Recall · July 2, 2026
Sanven Technology Ltd., dba Vevor, of Rancho Cucamonga, California
VEVOR baby loungersThe recalled baby loungers violate the mandatory safety standard for infant sleep products. The sides are too low to contain an infant and the enclosed openings at the foot of the loungers are wider than allowed, posing serious risks of fall and entrapment hazards to infants. In addition, the baby loungers do not have a stand, posing a fall hazard if used on elevated surfaces. These violations create an unsafe sleeping environment and can cause death or serious injury.
- Unclassified
Consumer Product Recall · July 2, 2026
Groupe SEB USA dba Rowenta USA, of Parsippany, New Jersey
Rowenta Cordless Vacuum Cleaners with lithium-ion batteryThe recalled lithium-ion battery in the vacuum cleaner can overheat and ignite, posing a risk of serious injury from fire and burn hazards.
- Class II
Medical Device Recall · July 2, 2026
OsteoBallast, 45 x 17.5 mm (SeaSpine Brand), REF: 56800095. Ballast, 45 x 17.5 mm (IsoTis Brand), REF: 02-8000-095Demineralized bone matrix (DBM) in resorbable mesh indicated for use with autograft as a bone graft extender in the posterolateral spine and pelvis, were filled with approx. 4.5 cc DBM (fill for 45 ¿ 11 mm configuration) instead of approx. 7.5 cc DBM (fill for 45 ¿ 17.5 mm configuration), which may lead to delayed fusion, incomplete fusion, pseudarthrosis, or lack of bone ingrowth.
- Unclassified
Consumer Product Recall · July 2, 2026
Winco Fireworks International, LLC, of Grandview, Missouri
Roman Candles 8 Shot 3-Pack Firework DevicesThe recalled fireworks can malfunction, and shots can blow out the side of the tube, posing a risk of serious injury from explosion and burn hazards.
- Unclassified
Consumer Product Recall · July 2, 2026
Diamond Wipes International, Inc. of Chino, California
CVS Health Medicated Hemorrhoidal WipesThe recalled medicated wipes contain lidocaine, which must be in child-resistant packaging, as required by the Poison Prevention Packaging Act. The packaging of the wipes is not child-resistant, posing a risk of serious injury or death from poisoning if the contents of the wipes are ingested by young children.
- Unclassified
Consumer Product Recall · July 2, 2026
Cooper Lighting, LLC, of Peachtree City, Georgia
Metalux Optimized High Bay (OHB) LED Light FixturesThe LED's board can overheat or come into contact with the lens or nearby combustible materials, posing a fire hazard.
- Unclassified
Consumer Product Recall · July 2, 2026
Winco Fireworks International, LLC, of Grandview, Missouri
Unity 7 Shot 200 Gram Aerial Cake Firework DevicesThe recalled fireworks can tip over, posing a risk of serious injury from explosion and burn hazards.
- Unclassified
Consumer Product Recall · July 2, 2026
Xishentang Dongguan Trading Co, Ltd., dba Pretty-Life, of China
AMASKY Nursing PillowsThe recalled nursing pillows advertised for infant feeding and tummy time violate the mandatory safety standards for nursing pillows and infant support cushions because they can obstruct an infant's breathing, posing a serious risk of injury or death from suffocation.
- Unclassified
Consumer Product Recall · July 2, 2026
Conair LLC, of Stamford, Connecticut
Metal Wire Bristle Grill BrushesSmall metal wire bristles can detach from the brushes and stick to the grill or food, posing an ingestion hazard and risk of serious internal injuries that could require surgery.
- Unclassified
Consumer Product Recall · July 2, 2026
Changzhou Niujie Battery Technology Co., Ltd., dba JSNJ_Tech, of China
Junpower CR2032 BatteriesThe lithium coin batteries are not sold in child-resistant packaging and do not bear the warning labels as required under Reese's Law. When button cell or coin batteries are swallowed, the ingested batteries can cause serious injuries, including internal chemical burns and death.
- Unclassified
Consumer Product Recall · July 2, 2026
Shenzhen Bopu Product Design Co., Ltd., dba POPOOO, of China
POPOOO Jungle Safari LED Finger LightsThe recalled LED finger lights violate the mandatory safety standard for toys because they contain 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
Consumer Product Recall · July 2, 2026
Target, of Minneapolis, Minnesota
Gigglescape™ Under the Sea Popping ToyThe clear plastic dome can detach from the blue plastic base, making the small plastic balls inside the toy accessible to children, posing a choking hazard.
- Unclassified
Vehicle Recall · July 2, 2026
2023 KIA TELLURIDE, 2024 KIA TELLURIDEA fire increases the risk of injury.
- Class II
Food Recall · July 2, 2026
Brooklyn Roasting Company Pasteurized Cold Brew Concentrate; 2.5gal; bag in a box distributed between 04/01/2026 and 06/20/2026.Ambient storage of the product may lead to Clostridium botulinum toxin formation.
- Class II
Medical Device Recall · July 1, 2026
Intramedullary Bone Saw Blade Assembly Model/Catalog Number: 475635 Product Description: Intramedullary Bone Saw Blade Assembly 15mmZimmer Biomet is conducting a medical device recall removal for various sizes of the Intramedullary Bone Saw Blade Assembly due to potential sterile barrier packaging damage caused by an exposed saw blade.
- Class II
Medical Device Recall · July 1, 2026
Stryker Hoffmann II Connecting Rod Micro 3 x 50mm. Catalog Number: 50796050.Potential cracking of the Hoffmann II Carbon Connecting Rods following cleaning and sterilization.
- Class II
Medical Device Recall · July 1, 2026
Intramedullary Bone Saw Blade Assembly Model/Catalog Number: 475620 Product Description: Intramedullary Bone Saw Blade Assembly 12mmZimmer Biomet is conducting a medical device recall removal for various sizes of the Intramedullary Bone Saw Blade Assembly due to potential sterile barrier packaging damage caused by an exposed saw blade.
- Class II
Medical Device Recall · July 1, 2026
Cardiac Workstation 5000. Product Number: 860439.Device will intermittently provide inaccurate data related to native heart rate.
- Class II
Medical Device Recall · July 1, 2026
Stryker Hoffmann II Connecting Rod Micro 3 x 60mm. Catalog Number: 50796060.Potential cracking of the Hoffmann II Carbon Connecting Rods following cleaning and sterilization.
- Class II
Medical Device Recall · July 1, 2026
5-PLASMA Bivalirudin Calibrator, Model Number 5D-46905Stability issues with the reconstituted lyophilized human plasma and bivalirudin matrix have been identified. These stability issues lead to a degradation of measurable bivalirudin in the controls, calibrators, and linearity values.
- Class II
Medical Device Recall · July 1, 2026
Cardiac Workstation 7000. Product Number: 860441.Device will intermittently provide inaccurate data related to native heart rate.
- Class II
Medical Device Recall · July 1, 2026
Stryker Hoffmann II Connecting Rod Micro 3 x 120mm. Catalog Number: 50796120.Potential cracking of the Hoffmann II Carbon Connecting Rods following cleaning and sterilization.
- Unclassified
Vehicle Recall · July 1, 2026
2023 BMW X1, 2023 BMW X7, 2023 BMW XM, 2024 BMW X1, 2024 BMW X5, 2024 BMW X6, 2024 BMW X7, 2024 BMW XM, 2024 BMW 530I, 2024 BMW I5, 2025 BMW I5, 2025 BMW X7, 2025 BMW X6, 2025 BMW X5, 2025 BMW I7, 202A loss of power brake assist can extend the distance required to stop the vehicle. Additionally, malfunctioning ABS and/or DSC systems can cause a loss of vehicle control. Either of these scenarios can increase the risk of a crash.
- Class II
Medical Device Recall · July 1, 2026
Intramedullary Bone Saw Blade Assembly Model/Catalog Number: 475630 Product Description: Intramedullary Bone Saw Blade Assembly 14mmZimmer Biomet is conducting a medical device recall removal for various sizes of the Intramedullary Bone Saw Blade Assembly due to potential sterile barrier packaging damage caused by an exposed saw blade.
- Class II
Food Recall · July 1, 2026
Mellish Island Super Skin; Dietary Supplement; 60 Capsules, 2 per day; Distributed by Mellish Island Corp. UPC: 8 58792 00332 3Firm's finished product label does not declare the source of marine collagen which was determined to be fish.
- Class II
Medical Device Recall · July 1, 2026
5-PLASMA Bivalirudin Control, Model Number 5D-44905Stability issues with the reconstituted lyophilized human plasma and bivalirudin matrix have been identified. These stability issues lead to a degradation of measurable bivalirudin in the controls, calibrators, and linearity values.
- Class II
Medical Device Recall · July 1, 2026
Intramedullary Bone Saw Blade Assembly Model/Catalog Number: 475625 Product Description: Intramedullary Bone Saw Blade Assembly 13mmZimmer Biomet is conducting a medical device recall removal for various sizes of the Intramedullary Bone Saw Blade Assembly due to potential sterile barrier packaging damage caused by an exposed saw blade.
- Class II
Medical Device Recall · July 1, 2026
Stryker Hoffmann II Connecting Rod Micro 3 x 40mm. Catalog Number: 50796040.Potential cracking of the Hoffmann II Carbon Connecting Rods following cleaning and sterilization.
- Class I
Drug Recall · July 1, 2026
Victory Medical Center Pharmacy
Glutathione (MDV), 200 mg/mL, 30 mL vial, each mL contains Glutathione 200 mg, Ascorbic Acid 20 mg, Benzyl Alcohol 1.5%, Na Hydroxide (Ph Adjust) in sterile water for injection, VMC.Microbial Contamination of Sterile Products - out of specifications results were obtained for bacterial endotoxin.
- Class II
Medical Device Recall · July 1, 2026
Intramedullary Bone Saw Blade Assembly Model/Catalog Number: 475640 Product Description: Intramedullary Bone Saw Blade Assembly 16mmZimmer Biomet is conducting a medical device recall removal for various sizes of the Intramedullary Bone Saw Blade Assembly due to potential sterile barrier packaging damage caused by an exposed saw blade.
- Class II
Medical Device Recall · July 1, 2026
Stryker Hoffmann II Connecting Rod Micro 3 x 30mm. Catalog Number: 50796030.Potential cracking of the Hoffmann II Carbon Connecting Rods following cleaning and sterilization.
- Class II
Food Recall · July 1, 2026
FLOUNDER SASHIMI WITH SAUCE; Keep Frozen; Net WT: 300g; UPC: 8 809342 366186Foreign Manufacturer label contains Undeclared allergen ingredients Wheat, Soy, Sesame, Yellow #5 and Blue #1 in Frozen Flounder Products.
- Class II
Medical Device Recall · July 1, 2026
Stryker Hoffmann II Connecting Rod Micro 3 x 150mm. Catalog Number: 50796150.Potential cracking of the Hoffmann II Carbon Connecting Rods following cleaning and sterilization.
- Class II
Food Recall · July 1, 2026
Sliced Korean Halibut with Soy sauce, Wasabi, Vinegar Chili Paste; Keep Frozen; Net WT: 12.2OZ (374g); UPC: 6 78108 16991 4Foreign Manufacturer label contains Undeclared allergen ingredients Wheat, Soy, Sesame, Yellow #5 and Blue #1 in Frozen Flounder Products.
- Class II
Medical Device Recall · July 1, 2026
5-PLASMA Bivalirudin AMR Verification Kit, Model Number 5D-45905Stability issues with the reconstituted lyophilized human plasma and bivalirudin matrix have been identified. These stability issues lead to a degradation of measurable bivalirudin in the controls, calibrators, and linearity values.
- Class II
Medical Device Recall · July 1, 2026
Stryker Hoffmann II Connecting Rod Micro 3 x 90mm. Catalog Number: 50796090.Potential cracking of the Hoffmann II Carbon Connecting Rods following cleaning and sterilization.
- Class II
Food Recall · July 1, 2026
Ultimate Mother's Day Wangshin Doenjang Aged 3 Years 9 oz. Korean Traditional Premium Soybean Paste UPC: 8 809897 940169Product label allergen "contains" statement does not include anchovy(fish)
- Class II
Medical Device Recall · June 30, 2026
Merge OrthoPACS, medical imaging diagnostic workstationThumbnails from a previously opened patient study may be displayed in the Thumbnail Bar while a different patient study is currently open.