Safety Recalls
RSS ↗15,186 recalls across FDA food, drug, and medical device recalls, CPSC consumer products, and NHTSA vehicles.
Showing 3,201–3,250 of 15,186
- Class II
Food Recall · November 20, 2025
Anti-virus Herbal Supplement, 1:5 Alcohol Tincture, Helps to stop viral replication, expectorant properties, Contains: Forsethia blossoms, Sumac berries, Pine needles; packaged in a 2 oz. glass droppeUnapproved drug claims on product labeling and product misbranded due to no Supplement Facts label
- Class I
Food Recall · November 20, 2025
Doughy brand Chocolate Chip Cookie Dough; 12 ozProduct may be contaminated with Salmonella
- Class II
Food Recall · November 20, 2025
Boswellia Herbal Supplement, 1:5 Alcohol Double Extract, Extracted from Frankincense with powerful anti-inflammatory properties, useful for pain & inflammation; packaged in a 2 oz. glass dropper bottlUnapproved drug claims on product labeling and product misbranded due to no Supplement Facts label
- Class II
Food Recall · November 20, 2025
Organic Ginger Root Herbal Supplement, Natural anti-inflammatory properties, supports gut, increases circulation, 50 capsules/560 mg, packaged in a plastic bagUnapproved drug claims on product labeling and product misbranded due to no Supplement Facts label
- Class II
Food Recall · November 20, 2025
Chaga Mushroom Herbal Supplement, 1:5 Alcohol Double Extract, Supports a healthy immune system with anti-cancer properties; packaged in a 2 oz. glass dropper bottle, UPC 284588087831Unapproved drug claims on product labeling and product misbranded due to no Supplement Facts label
- Unclassified
Consumer Product Recall · November 20, 2025
AliExpress, of San Mateo, California
4-in-1 Baby Safety Cart CarriageThe stroller violates the mandatory standard for strollers because the restraint system can fail, posing a risk of serious injury or deadly fall hazard.
- Unclassified
Consumer Product Recall · November 20, 2025
Shenzhenshiruoxuandianzishangwuyouxiangongsi doing business as Nuoxuann, of China
Bearlala Baby LoungersThe recalled baby loungers violate the mandatory standard for Infant Sleep Products. The sides are too low to contain an infant. The enclosed openings at the foot of the loungers are wider than allowed, posing 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 to infants.
- Unclassified
Consumer Product Recall · November 20, 2025
STARKİM KİMYA SAN. T.C. A.Ş., of Turkey
MoonSoll and Magic Chems Fuel BottlesThe ethanol fuel bottles violate the federal safety standard for portable fuel containers because they lack flame mitigation devices required by the Portable Fuel Container Safety Act, posing a deadly risk of flash fire. The fuel containers also fail to meet the federal safety regulation for deceptive disclaimers required by the Federal Hazardous Substances Act (FHSA) because they claim the contents are "Non-Toxic."
- Unclassified
Consumer Product Recall · November 20, 2025
LPA1, LLC dba Little Partners, of Exton, Pennsylvania
Grow 'N Stow Folding Learning TowerThe platform inside the tower can collapse, posing a fall hazard to young children.
- Unclassified
Consumer Product Recall · November 20, 2025
Guangzhou Tinger Trading Co. Ltd., of China doing business as Anna Queen
Play YardsThe play yards violate the mandatory standard for play yards. Infants can become entrapped under the mattress or between the side of the play yard and the mattress, posing a risk of serious injury or deadly suffocation hazard.
- Unclassified
Consumer Product Recall · November 20, 2025
Anzmtosn Magnet Fidget Spinner SetsThe recalled magnet spinner sets violate the mandatory standard for toys because the sets contain loose 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 · November 20, 2025
Baituo Innovation Technology Co. Ltd., dba Romorgniz, of China
Romorgniz Fabric 12- and 13-Drawer DressersThe recalled dressers are unstable if they are not anchored to the wall, posing serious tip-over and entrapment hazards that can result in injuries or death to children. The dressers violate the mandatory standard as required by the STURDY Act.
- Class II
Medical Device Recall · November 19, 2025
AMSCO 7052HP Washer/Disinfector Model/Catalog Number: 7052HP Product Description: The AMSCO 7052HP Washer/Disinfector is intended for use in the cleaning and intermediate-level disinfection of soWire connected to the electrical box may shift out of its intended position, which may result in electrical arcing. Electrical arcing remains internal within the unit (no risk of shock to users).
- Class II
Medical Device Recall · November 19, 2025
AMSCO 7053HP Washer/Disinfector Model/Catalog Number: 7053HP Product Description: The AMSCO 7053HP Washer/Disinfector is intended for use in the cleaning and intermediate-level disinfection of sWire connected to the electrical box may shift out of its intended position, which may result in electrical arcing. Electrical arcing remains internal within the unit (no risk of shock to users).
- Class I
Food Recall · November 19, 2025
Sonex brand aluminum pot; ISO 9001:2000; Made in PakistanProducts found to contain leachable lead levels (0.323mg/L)
- Class II
Food Recall · November 19, 2025
DPA161 Shrimp Paste (Klong Kone) 'L' , 32 oz, 12 count , PLastic Jar, 12 packages / casesProduct tested high for lead.
- Class II
Medical Device Recall · November 19, 2025
Vortex Surgical 25ga Illuminated Flex-Tip Laser Probe, Catalog Number VS0135.25;Reason for the voluntary recall is some products in this lot are not passing through a 25ga cannula smoothly.
- Class II
Food Recall · November 19, 2025
Shrimp Paste (Klong Kone) 'M' , 16 oz, 24 count , PLastic Jar, 24 packages/ caseProduct tested high for lead.
- Class III
Food Recall · November 19, 2025
Preserved Mustard in Soybean Oil; original packaging is predominantly green with gold accents and black Chinese lettering. UPC: 6 927393 804265Undeclared allergen ingredient (wheat).
- Class II
Food Recall · November 19, 2025
Chef brand Milk Pan 24cmProducts found to contain leachable lead levels (3.00 mg/L)
- Class II
Medical Device Recall · November 18, 2025
Brand name: AGFA Digital Radiography X- Ray system DR 800 with MUSICA Dynamic Common Name: DR 800It is possible to exceed the maximum allowed Air Kerma rate (AKR) of 88mGy/min for pulsed fluoro exams. This can happen in case the framerate is increased on the NX workstation when ABS is not enabled.
- Class II
Medical Device Recall · November 18, 2025
Mindray DS USA, Inc. dba Mindray North America
Hardware configuration of the BeneVision Central Monitoring System (CMS), marketed as BeneVision Distributed Monitoring System (DMS). Model Number: 115-050935-00 and E115-050935-00. Software Version:When the Worstation of the BeneVision DMS has a specific hardware configuration, the computer may experience audio playback failure or screen freezing.
- Class II
Food Recall · November 18, 2025
Simplot¿ Traditional Reduced Sodium Tater Gems¿ , formed frozen potatoes, 6/5lb bags per case, foodservice item, master case UPC 100 71179 00418 9. Distributed by Simplot Global Food, LLC, P.O. Box 9Plastic fragments. Pieces of semi-rigid plastic embedded in the recalled Tater Gems product.
- Class III
Drug Recall · November 18, 2025
Glenmark Pharmaceuticals Inc., USA
Nebivolol Tablets, 20 mg, 90 Tablets, Rx Only, Manufactured by: Glenmark Pharmaceuticals Limited, Pithampur, Madhya Pradesh 454775, India, Manufactured for Avkare, Pulaski, TN 38478, Product of Italy,Cross Contamination with Other Products
- Class II
Medical Device Recall · November 18, 2025
Intelerad InteleShare software, with ProViewer componentSoftware intended to aid in diagnosing conditions, planning treatments, visualizing anatomical structures has a bug that, if all of following are met: Viewing images in InteleShare viewer; Multiplanar reconstruction applied; Manual rotation applied, could result in inaccurate length measurement tool values that could compromise diagnostic accuracy, lead to misdiagnosis or inappropriate follow-up.
- Class III
Medical Device Recall · November 18, 2025
HemosIL SynthAFax. Partial Thromboplastin Time Tests.Recalled lots were manufactured with double the amount of preservative concentration.
- Class II
Food Recall · November 18, 2025
Karabetian Import and Distribution, Inc.
Product: Zimi Kunefe Ready to eat (Frozen) Package Size and quantity per case: 380 g paper carton/tray - 9/case UPC: 5201592015822partially hydrogenated oils (PHOs) in foods exported to the US
- Class II
Food Recall · November 18, 2025
Karabetian Import and Distribution, Inc.
Product: Zimi Puff Pastry French Style (frozen) Package Size and quantity per case: 700 g paper carton - 12/case UPC: 5201592020017. Frozen.partially hydrogenated oils (PHOs) in foods exported to the US
- Class II
Medical Device Recall · November 17, 2025
SEASPINE ORTHOPEDICS CORPORATION
Orthofix NorthStar OCT Navigation Surgical Technique Guide, and instruments: Navigation Driver, REF: PC2-400012; Navigation Straight Bone Probe, REF: PC2-400013; Navigation, 3.5mm Drill, REF: PC2-400The NorthStar OCT Navigation Surgical Technique Guide (STG) incorrectly identified both Medtronic s Solera and Medtronic s Infinity system toolcards as compatible with the NorthStar OCT Navigation Instruments. However, the NorthStar OCT Navigation Instruments are compatible for use with Medtronic s Solera toolcards only.
- Class II
Medical Device Recall · November 17, 2025
The Pressio 2 ICP Monitoring System, Model Number PSO-4000; Intracranial Pressure MonitorCustomer complaints of Pressio monitor rebooting.
- Class II
Medical Device Recall · November 17, 2025
Sheathes3D Seamless Viral Barrier, Latex-Free, 7/8"D Tapered to 2.9"W x 11.8"L (2.2cm Tapered to 7.4cm x 30cm), Non-Sterile, Ultrasound Probe Cover, Vaginal/Rectal, Tapered, Rolled, Extra-Long, IndiviVaginal/rectal ultrasound probe covers with a viral barrier may have product defects, which may result in contamination during use, posing an infection risk.
- Class II
Medical Device Recall · November 17, 2025
Brand Name: Molift Product Name: Molift 4-point sling bars (Accessory to mobile hoists) Model/Catalog Number: 1430116,1430117,1430115 Product Description: The mobile hoist is an assistive device inA customer experienced that during assembly and load testing of the device, the bolt for mounting the lifting bar broke. Upon further investigation of this customer complaint, it became clear that the defect occurs as a result of deformation of the materials involved between the lifting bar and the arm of the device. Such deformation can lead to limited mobility in the joint, which prevents proper functionality of the equipment.
- Class II
Drug Recall · November 17, 2025
Preferred Pharmaceuticals, Inc.
Ondansetron ODT Tablets, USP 4mg, 1x10 unit dose tablets, Mfg: Glenmark Pharmaceuticals Limited, Repackaged by Preferred Pharmaceuticals NDC 68788-8666-01Defective container: Preferred Pharmaceuticals received a letter from the manufacturer Glenmark, that the blister packs are not fully sealed and tablets falling out. Preferred Pharmaceuticals purchased the finished product and repackaged the product for sale.
- Class II
Medical Device Recall · November 17, 2025
Brand Name: Molift Product Name: Molift Mover 205 Model/Catalog Number: (1) M14000, (2) M1401, (3) M1402, (4) M14050, (5) M14150, (6) M1402-01, (7) M14050-00 (8) M14001;A customer experienced that during assembly and load testing of the device, the bolt for mounting the lifting bar broke. Upon further investigation of this customer complaint, it became clear that the defect occurs as a result of deformation of the materials involved between the lifting bar and the arm of the device. Such deformation can lead to limited mobility in the joint, which prevents proper functionality of the equipment.
- Class II
Medical Device Recall · November 17, 2025
Brand Name: Molift Product Name: Molift 2-point sling bars (Accessory to mobile hoists) Model/Catalog Numbers: (1) 1530101, (2) 1530102 Product Description: The mobile hoist is an assistive deviceA customer experienced that during assembly and load testing of the device, the bolt for mounting the lifting bar broke. Upon further investigation of this customer complaint, it became clear that the defect occurs as a result of deformation of the materials involved between the lifting bar and the arm of the device. Such deformation can lead to limited mobility in the joint, which prevents proper functionality of the equipment.
- Class II
Medical Device Recall · November 17, 2025
Brand Name: Molift Product Name: Molift Mover 300 Model/Catalog Numbers: (1) M1501, (2) M1502, (3) M1504, (4) M15050, (5) M15151, (6) M15001, (7) M15002; Product Description: The mobile hoist is anA customer experienced that during assembly and load testing of the device, the bolt for mounting the lifting bar broke. Upon further investigation of this customer complaint, it became clear that the defect occurs as a result of deformation of the materials involved between the lifting bar and the arm of the device. Such deformation can lead to limited mobility in the joint, which prevents proper functionality of the equipment.
- Class II
Medical Device Recall · November 17, 2025
Da Vinci 5 ASSY, DV5 CONSOLE, IS5000 Model/Catalog Number: 380730 Used for minimally invasive surgery.An error event following the release of a software version for the surgical system that can result in loss of user interface content on an external monitor or tower monitor.
- Class II
Food Recall · November 16, 2025
Lava Bun with Salted Egg Yolk orange packaging (Frozen) Unsalted butter and cream are listed in the ingredient statement.Products do not declare milk in the Contains statement or the ingredient statement.
- Class II
Food Recall · November 16, 2025
Lava Bun with Green Tea Flavor bright lime green packaging (Frozen) Unsalted butter and cream are listed in the ingredient statement.Products do not declare milk in the Contains statement or the ingredient statement.
- Class I
Food Recall · November 16, 2025
Charlevoix Cheese Company Mild Cheddar Cheese, Net Wt. 8 oz (227g). UPC 8 50056-64205 7. 12 retail units per wholesale case.Possible Listeria monocytogenes contamination.
- Class II
Medical Device Recall · November 14, 2025
Olympus Corporation of the Americas
Brand Name: ShockPulse-SE Lithotripsy System SPL-S Product Name: ShockPulse-SE Lithotripsy System - Single Use Probes Model/Catalog Number: SPL-S Product Description: The ShockPulse Lithotripsy SysOngoing investigations identified additional instances of the device Generator remaining in a blinking phase waiting to recognize the transducer. Damage to the transducer plug and/or generator receptacle may cause these issues.
- Class II
Medical Device Recall · November 14, 2025
Olympus Corporation of the Americas
Brand Name: ShockPulse-SE Lithotripsy System SPL-SR Product Name: ShockPulse-SE Lithotripsy System - Reusable Probes Model/Catalog Number: SPL-SR Product Description: The ShockPulse Lithotripsy SysOngoing investigations identified additional instances of the device Generator remaining in a blinking phase waiting to recognize the transducer. Damage to the transducer plug and/or generator receptacle may cause these issues.
- Class II
Medical Device Recall · November 14, 2025
Halyard, MIDTOWN GENERAL ARTERIOGRAM. Catalog Number: EUHM009-01.Potential for incomplete seal on header bag.
- Class I
Food Recall · November 14, 2025
Face Rock Creamery Vampire Slayer Garlic Cheddar, net wt. 6oz. Ready to Eat, Refrigerated/ Perishable. Product is packaged in sealed in bag and shrink dipped. UPC 8 51222 00547 8. Face Rock Creamery,FDA environmental sample identified the presence of Listeria monocytogenes in the processing area where cheese was packaged.
- Class I
Medical Device Recall · November 14, 2025
GE Medical Systems China Co., Ltd.
GE Healthcare Carestation anesthesia system Power Management Board (PMB) Field Replaceable Unit (FRU), 2076139-001-SPotential unexpected shutdown of Carestation 600 and 700 Series Anesthesia Systems containing certain power management boards, if the AC mains power is unplugged or in the event of an AC mains power failure. Anesthesia systems only operate on battery power in a rare event that AC mains power is lost and there is no continuous backup emergency power. If AC power is interrupted, the system will not automatically switch over to the battery supply mode and will reboot. If this issue occurs, a temporary disruption of mechanical ventilation, manual ventilation, and volatile agent delivery may occur. Following the reboot, the system will not return to the previous ventilation settings.
- Class II
Drug Recall · November 14, 2025
Cinacalcet Hydrochloride Tablets, 30 mg, 30 Tablets per bottle, Rx Only, Manufactured for: Cipla USA, Inc., 10 Independence Boulevard, Suite 300, Warren, NJ 07059. NDC: 69097-410-02CGMP Deviations: the presence of a nitrosamine impurity, N-nitroso-cinacalcet, above the acceptable daily intake (ADI) limits.
- Class II
Medical Device Recall · November 14, 2025
Halyard, MAJOR PACK. Catalog Number: JEMJ10-01.Potential for incomplete seal on header bag.
- Class II
Drug Recall · November 14, 2025
Cinacalcet Hydrochloride Tablets, 60 mg, 30 Tablets per bottle, Rx Only, Manufactured for: Cipla USA, Inc., 10 Independence Boulevard, Suite 300, Warren, NJ 07059. NDC: 69097-411-02CGMP Deviations: the presence of a nitrosamine impurity, N-nitroso-cinacalcet, above the acceptable daily intake (ADI) limits.
- Class I
Medical Device Recall · November 14, 2025
Ivenix Infusion System (IIS), LVP Software LVP-SW-0005. Software for the controlled administration of fluids to patients.Software version 5.10.1 and earlier contain anomalies that have the potential to cause serious patient harm or death.
- Class II
Medical Device Recall · November 14, 2025
Olympus Corporation of the Americas
Brand Name: ShockPulse-SE Lithotripsy System Product Name: ShockPulse-SE Lithotripsy System - Generator Model/Catalog Number: SPL-G Product Description: The ShockPulse Lithotripsy System is an elecOngoing investigations identified additional instances of the device Generator remaining in a blinking phase waiting to recognize the transducer. Damage to the transducer plug and/or generator receptacle may cause these issues.