Safety Recalls
RSS ↗15,264 recalls across FDA food, drug, and medical device recalls, CPSC consumer products, and NHTSA vehicles.
Showing 5,601–5,650 of 15,264
- Class II
Food Recall · July 11, 2025
YoCrunch Lowfat Yogurt with Toppers. Two-product package. Contains 8-6oz (170g) cups of Vanilla Yogurt with Snickers pieces (cup UPC 46675-00112), and 8-6oz (170g) cups of Vanilla Yogurt with Twix bForeign material (plastic pieces)
- Class II
Food Recall · July 11, 2025
YoCrunch Low Fat Yogurt with toppers. Vanilla with Oreo cookie pieces, Packaged in the following size containers: 1. Single Serve Cup, 6 oz. (170g) UPC 46675-00080 2. Multipack containing 4-4 ozForeign material (plastic)
- Class II
Food Recall · July 11, 2025
YoCrunch Low Fat Yogurt with Toppers, Vanilla with Snickers pieces, Packaged in the following size containers: 1. Single Serve Cup, 6 oz. (170g) UPC 46675-00112 2. Multipack containing 4-4 oz. cuForeign material (plastic pieces)
- Class II
Food Recall · July 11, 2025
YoCrunch Lowfat Yogurt with Toppers. Two-product packages. 1. Contains 8- 6oz (170g) cups of Vanilla Yogurt with milk chocolate M&Ms pieces (cup UPC 46675-00079), and 8-6oz (170g) cups of VanillaForeign material (plastic pieces)
- Class II
Food Recall · July 11, 2025
YoCrunch Low Fat Yogurt with Toppers, Vanilla with Chocolate Chip Cookie Dough pieces, Multipack containing 4-4 oz. (113g) cups. UPC 46675-01315. Keep Refrigerated. Distributed by Danone US, LLC,Foreign material (plastic pieces)
- Class II
Food Recall · July 11, 2025
YoCrunch Low Fat Yogurt with Toppers, Strawberry with Granola pieces, Single Serve Cup, 6 oz. (170g) UPC 46675-00010. Keep Refrigerated. Distributed by Danone US, LLC, White Plains, NY 10605Foreign material (plastic pieces)
- Class I
Medical Device Recall · July 11, 2025
Plum Duo Infusion System, List Number: 400020401ICU Medical identified two sequences of programming events and alarm interactions that may cause the user interface to become unresponsive.
- Class II
Food Recall · July 11, 2025
YoCrunch Low Fat Yogurt with Toppers, Vanilla with Twix bar pieces, Packaged in the following size containers: 1. Single Serve Cup, 6 oz. (170g) UPC 46675-00113 2. Multipack containing 4-4 oz. cupForeign material (plastic pieces)
- Class I
Medical Device Recall · July 11, 2025
Flexicare Medical (Dongguan) Ltd.
BritePro Solo Mini with Pro Miller Blade Size 1.5, REF:040-02-0415ULaryngoscope handles may not illuminate as intended.
- Class I
Medical Device Recall · July 11, 2025
Flexicare Medical (Dongguan) Ltd.
BritePro Solo Single-Use Fiber Optic Laryngoscope Handle Refs:040-310AU and 040-310ULaryngoscope handles may not illuminate as intended.
- Class II
Medical Device Recall · July 11, 2025
Blood/MacConkey Biplate 100/PK, Product Number R02049The products may contain surface and subsurface contamination of Listeria monocytogenes.
- Class II
Medical Device Recall · July 11, 2025
Strep Selective II Agar, Product Number R01859The products may contain surface and subsurface contamination of Listeria monocytogenes.
- Class I
Food Recall · July 10, 2025
Drycapot cookie, net weight: 1.15 oz UPC#: 4 942737 210191Undeclare Tree Nuts (almond, macadamia nut)
- Class I
Medical Device Recall · July 10, 2025
All-round Joystick R-net Light. Electrical wheelchair component.Devices with firmware versions 2.3 and lower may experience timing variations between software tasks, which could result in skipping the necessary neutral check and the wheelchair producing unintended movement upon power-up when the joystick is out of neutral.
- Class I
Medical Device Recall · July 10, 2025
IDM-MICRO-R. Electrical wheelchair component.Devices with firmware versions 2.3 and lower may experience timing variations between software tasks, which could result in skipping the necessary neutral check and the wheelchair producing unintended movement upon power-up when the joystick is out of neutral.
- Class II
Medical Device Recall · July 10, 2025
Access Thyroglobulin assay, a simultaneous one-step immunoenzymatic assay, Catalog Number 33860Access Thyroglobulin reagent lot 439163 may generate erroneously high patient results. Falsely increased Access Thyroglobulin results may lead a physician to pursue unnecessary diagnostic imaging studies and/or inappropriate therapy adjustments in patients being monitored for residual or recurrent thyroid cancer.
- Class I
Medical Device Recall · July 10, 2025
IDM-MULTI-R. Electrical wheelchair component.Devices with firmware versions 2.3 and lower may experience timing variations between software tasks, which could result in skipping the necessary neutral check and the wheelchair producing unintended movement upon power-up when the joystick is out of neutral.
- Class II
Drug Recall · July 10, 2025
Power Stick for her PH Balanced Roll-On Antiperspirant Deodorant with Powder Fresh Scent, 1.8 oz./53 mL, A.P Deauville, LLC, PA 18040, NDC# 42913-038-00, UPC Code 815195019313CGMP Deviations
- Class I
Food Recall · July 10, 2025
FANCY MEDIUM PECAN PIECES 81124 561958 554707 6/13/2025 SDC1645 90 FANCY MEDIUM PECAN PIECES 81124 561965 554714 6/13/2025 SDC1645 90 FANCY MIDGET PECAN PIECES 81086 561845 554594 5/30/2025 SDC1505 5Pecans have the potential to be contaminated with Salmonella,
- Class I
Medical Device Recall · July 10, 2025
IDM-ARLITE-R. Electrical wheelchair component.Devices with firmware versions 2.3 and lower may experience timing variations between software tasks, which could result in skipping the necessary neutral check and the wheelchair producing unintended movement upon power-up when the joystick is out of neutral.
- Class I
Medical Device Recall · July 10, 2025
Multi Joystick R-net. Electrical wheelchair component.Devices with firmware versions 2.3 and lower may experience timing variations between software tasks, which could result in skipping the necessary neutral check and the wheelchair producing unintended movement upon power-up when the joystick is out of neutral.
- Class III
Medical Device Recall · July 10, 2025
Description/REF: BD PYXIS MEDBANK MINI 1FH-1FM/169-137, BD PYXIS MEDBANK MINI 4HM/169-113, BD PYXIS MEDBANK MINI 4HH/169-112, BD PYXIS MEDBANK MINI 3HH-1HM/169-111, BD PYXIS MEDBANK MINI 3HH-1Reports of delayed access to medication in automated dispensing cabinets because of the override/Add Item workflow.
- Class I
- Unclassified
Vehicle Recall · July 10, 2025
Toyota Motor Engineering & Manufacturing
2025 TOYOTA SIENNA HYBRIDImproperly welded seat rails can prevent the seat from adequately restraining an occupant during a crash, increasing the risk of injury.
- Unclassified
Vehicle Recall · July 10, 2025
2023 LUCID AIR, 2024 LUCID AIR, 2025 LUCID AIRA rearview image that does not appear or fails to accurately depict behind the vehicle increases the risk of a crash.
- Unclassified
Vehicle Recall · July 10, 2025
2024 LUCID AIR, 2025 LUCID AIRA disconnected half shaft can result in a loss of drive power, increasing the risk of a crash.
- Unclassified
Consumer Product Recall · July 10, 2025
Shenzhenshi Yixiakejiyouxiangongsi, dba YIXIA, of China
AUGNORYE Padded Cushioned Crib BumpersThe recalled padded cushioned crib bumpers violate the federal crib bumper ban because they can obstruct an infant's breathing, posing a suffocation hazard. This creates an unsafe sleeping environment for infants. Padded crib bumpers are banned by the Safe Sleep for Babies Act.
- Unclassified
Consumer Product Recall · July 10, 2025
Fang Cheng Xian Hao Yun Shang Mao You Xian Gong Si, dba Haoyunm, of China
Braided crib bumpersThe recalled crib bumpers violate the federal ban on crib bumpers because the padded crib bumpers can obstruct breathing, posing a risk of serious injury or death to infants from suffocation. Padded crib bumpers are banned by the Federal Safe Sleep for Babies Act.
- Class II
Drug Recall · July 10, 2025
Bicillin L-A (penicllin G benzathine injectable suspension), 1,200,000 units per 2 mL, 2 mL-vial, Rx Only, Distributed by Pfizer Inc., New York, NY 10001. Made in Austria, Carton NDC - 60793-701-10,CGMP Deviations; particulates identified during visual inspection
- Unclassified
Consumer Product Recall · July 10, 2025
Giant Bicycle Inc., of Newbury Park, California
Momentum Vida E+ E-BikesThe fork steerer tube on the recalled bicycles can crack, break or separate during use, posing a fall hazard.
- Unclassified
Consumer Product Recall · July 10, 2025
Shenzhen Yihuachuang Technology, dba SPPTTY, of China
SPPTTY Kids 14- and 18-inch BicyclesMultiple components of the children's bicycles contain levels of lead that exceed the federal lead content ban, posing a lead poisoning hazard to children. In addition, the black paint on the bicycle pumps contains lead that exceeds the federal lead paint ban. Lead is toxic if ingested by young children and can cause adverse health issues.
- Class II
Drug Recall · July 10, 2025
Bicillin L-A (penicillin G benzathine injectable suspension), 2,400,000 units per 4 mL, 4ml-vial, Rx Only, Distributed by Pfizer Inc., New York, NY 10001, Made in Austria, Carton NDC- 60793-702-10 , SCGMP Deviations; particulates identified during visual inspection
- Class II
Medical Device Recall · July 10, 2025
FilmArray NGDS Warrior Panel NGDS-ASY-0007 is a qualitative, multiplexed, nucleic acid-based in vitro diagnostic test intended for use with the FilmArray 2.0 system.FilmArray NGDS Warrior Panel (NGDS-ASY-0007) has an increased risk of internal control failures when testing positive blood culture, which may lead to delayed results and additional diagnostic workup.
- Class I
Medical Device Recall · July 10, 2025
Micro Joystick R-net. Electrical wheelchair component.Devices with firmware versions 2.3 and lower may experience timing variations between software tasks, which could result in skipping the necessary neutral check and the wheelchair producing unintended movement upon power-up when the joystick is out of neutral.
- Unclassified
Consumer Product Recall · July 10, 2025
Zhongshan Hongtu Furniture Co., dba Kbabyea, of China
Creekliybear "Pack and Play" Aftermarket Play Yard MattressesThe aftermarket play yard mattresses violate the mandatory standard for crib mattresses as the mattresses exceed thickness requirements and may not adequately fit certain play yards, posing a deadly entrapment hazard. Babies can suffocate in gaps between an undersized mattress, or extra padding, and side walls of a product, especially when the infant's face becomes trapped against the side and the mattress, preventing the infant from breathing.
- Unclassified
Consumer Product Recall · July 10, 2025
Shaoxing Yishan Garment Co., Ltd., dba Signbaby, of China
Dearlomum Retractable Safety GatesThe recalled gates violate the federal standard for expansion gates and expandable enclosures because a child's torso can fit through the opening between the gate and the floor, posing a risk of serious injury or death due to entrapment hazard.
- Unclassified
Consumer Product Recall · July 10, 2025
Olympia Tools International Inc., of Covina, California
Ozark Trail 64 oz Stainless Steel Insulated Water BottlesThe lid can forcefully eject, posing serious impact and laceration hazards, when a consumer attempts to open the capped bottles after food, carbonated beverages or perishable beverages, such as juice or milk, are stored inside over time.
- Unclassified
Consumer Product Recall · July 10, 2025
Jiangsu Zhi Pai Furniture Manufacturing Co. Ltd., of China
WLIVE Fabric 15-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 federal standard as required by the STURDY Act.
- Class II
- Class I
Medical Device Recall · July 9, 2025
Ambu SPUR II Labeled as the following: 1 SPUR II Adult Resuscitator, Adult, Catalog Number: 523211000 2 SPUR II Adult Resuscitator w/Mercury Filter, Adult, Catalog Number: 523611051 3 SPUR II Adult RePotential for the manometer port being blocked rendering the manometer non-functional.
- Class III
- Class II
Drug Recall · July 9, 2025
Epinephrine Lidocaine HCL, 0.25mg/mL and 7.5 mg/mL, 20x1 mL Vials per carton, Rx Only, Imprimis NJOF, 1705 Route 46 West, Unit 6B Ledgewood, NJ, 07852 NDC: 71384-641-01Sub-Potent Drug: Subpotent assay results during stability testing.
- Class II
- Class II
- Class III
Drug Recall · July 9, 2025
Tropicamide-Proparacaine-Phenylephrine-Ketorolac, Sterile Ophthalmic Solution, 1% 0.5% 2.5% 0.5%, 5mL, 2x5ML vial per carton, Rx Only, Imprimis NJOF, LLC, 1705 Route 46 West, Unit 6B, Ledgewood, NJ 07Sub-Potent Drug: Subpotent assay results during stability testing.
- Class II
Medical Device Recall · July 9, 2025
Ortho-Clinical Diagnostics, Inc.
VITROS Chemistry Products Ca Slides; Catalog Number: 145 0261;Generations 67 and above of VITROS Ca Slides are experiencing an increased occurrence of Condition Code TH4-63J during calibration on VITROS XT 3400 and VITROS XT 7600 Systems, causing calibration failures that delay calcium test results and potentially impact patient management. The imaging reflectometer algorithm detects excessive "spikes" (imperfections) in slide images and generates the TH4-63J condition code when the threshold of 600 spikes is exceeded. Updated analysis revealed a 19-fold increase in failure rates from 0.0043% (2024 baseline) to 0.082% for Generation 67+ slides in 2025, with 100% of calibrator failures occurring at the lowest concentration level. This can result in delayed diagnosis and treatment of conditions such as hypercalcemic crisis, parathyroid disorders, and other calcium-related emergencies requiring urgent intervention.
- Class II
Medical Device Recall · July 9, 2025
Brand Name: EMPOWR 3D KNEE TIBIAL INSERT - E-PLUS Product Name: EMPOWR 3D KNEE INS, 7R 16MM, VE Model/Catalog Number: 342-16-707 Product Description: Enovis knee devices are intended for treatment oKnee implants contain incorrect labeling (size and/or side incorrect)
- Class II
Drug Recall · July 9, 2025
Cinacalcet Tablets 90 mg, 30-count bottles, Rx only, Manufactured by: Strides Pharma Science Ltd. Puducherry, India; Distributed by: Strides Pharma Inc. East Brunswick, NJ 08816, NDC 64380-885-04Failed Dissolution Specifications.