Safety Recalls
RSS ↗15,271 recalls across FDA food, drug, and medical device recalls, CPSC consumer products, and NHTSA vehicles.
Showing 6,251–6,300 of 15,271
- Unclassified
Consumer Product Recall · June 5, 2025
HTP residential gas boilersThe boiler door can fail to seal properly, due to incorrect burner door studs, allowing flames and gases to escape, posing fire and carbon monoxide (CO) poisoning hazards that can result in death or serious injury.
- Class I
Food Recall · June 5, 2025
Duo Spicy Calif Shrimp 10PcPotential contamination with Listeria monocytogenes
- Class II
Medical Device Recall · June 5, 2025
Custom Tubing Kit: REF: K04-00417, K04-00963, K04-01029High pressure tubing may relax over time causing it to partially separate from the connector resulting in a void that can trap air in the line. Use of the affected product may result in the trapped air being introduced into the patient.
- Class I
- Class II
Medical Device Recall · June 5, 2025
Custom Waste Management Kit: REF: K10-00353K, K10-01603C, K10-01694Q, K10-05159B, K10-05743, K10-05825APHigh pressure tubing may relax over time causing it to partially separate from the connector resulting in a void that can trap air in the line. Use of the affected product may result in the trapped air being introduced into the patient.
- Unclassified
Consumer Product Recall · June 5, 2025
Specialized Bicycle Components Inc., of Morgan Hill, California
Haul ST and LT E-bikes with telescopic seat postsWhen the lower portion of the e-bike's telescopic seat post is fully extended, the seat post can break, posing a fall hazard.
- Unclassified
Consumer Product Recall · June 5, 2025
BowFlex Inc., (formerly Nautilus Inc.), of Vancouver, Washington
BowFlex 552, 52.5 LB Adjustable Dumbbells and BowFlex 1090, 90 LB Adjustable DumbbellsThe weight plates can dislodge from the handle during use, posing an impact hazard.
- Unclassified
Consumer Product Recall · June 5, 2025
Yuanimi Trade Co. Ltd., d/b/a Ravmix, of China
Portable Hook-On ChairsThe recalled portable hook-on chair poses a deadly fall hazard because the crotch restraint can be removed without the use of a tool and infants can fall through an opening, which is a violation of the federal standard for portable hook-on chairs.
- Unclassified
Vehicle Recall · June 5, 2025
2025 HYUNDAI PALISADEA fire while parked or driving can increase the risk of injury.
- Class I
Food Recall · June 5, 2025
Crispy Shrimp Roll 10PcPotential contamination with Listeria monocytogenes
- Class I
Food Recall · June 5, 2025
Duo Crunchy Veg Shrimp 10PcPotential contamination with Listeria monocytogenes
- Class I
Food Recall · June 5, 2025
Rock N Roll Shrimp 10CtPotential contamination with Listeria monocytogenes
- Class II
Medical Device Recall · June 5, 2025
Brand Name: NIO-A Product Name: NIO Intraosseous Device Adult Model/Catalog Number: 105000603 Software Version: N/A Product Description: NIO devices are a spring-based, automatic intra-osseous accDue to manufacturing error, Intraosseous device built-in stabilizer may not be released properly after deployment and insertion.
- Class I
Food Recall · June 5, 2025
Duo Crispy Calif Shrimp 10PcPotential contamination with Listeria monocytogenes
- Class II
Medical Device Recall · June 5, 2025
Custom Manifold Kit: REF: K09-02239C, K09-02249UP, K09-09110B, K09-10294A, K09-11227A, K09-11456B, K09-12123B, K09-13342AP, K09-13391BP, K09-13548, K09-14000A, K09T-12020D, K09T-12275BHigh pressure tubing may relax over time causing it to partially separate from the connector resulting in a void that can trap air in the line. Use of the affected product may result in the trapped air being introduced into the patient.
- Class II
Medical Device Recall · June 5, 2025
High Pressure Tubing: REF: 502211002, HP9720E/C, HP9721E/CHigh pressure tubing may relax over time causing it to partially separate from the connector resulting in a void that can trap air in the line. Use of the affected product may result in the trapped air being introduced into the patient.
- Unclassified
Consumer Product Recall · June 5, 2025
Lutron Electronics Co. Inc., of Coopersburg, Pennsylvania
Lutron-branded power interfaces for LED tape lightsThe power interface can fail during a significant power surge (e.g., lightning strike), posing a shock hazard to consumers if they touch the LED tape lights.
- Unclassified
Consumer Product Recall · June 5, 2025
Direct Scaffold Supply LLC, of Houston, Texas
Casters on Direct Scaffold Supply Multi-Purpose Baker Style Scaffolding ProductsThe recalled casters can contain faulty spot welds that can cause them to break or fail, making the scaffolding unstable and posing a fall hazard.
- Unclassified
Consumer Product Recall · June 5, 2025
Generac Power Systems Inc., of Waukesha, Wisconsin
Battery-Powered ChainsawsThe motor controller of the recalled chainsaw can overheat during operation of the unit, posing fire and burn hazards.
- Unclassified
Consumer Product Recall · June 5, 2025
Shantou Jinshanglu Toys Industry Co. Ltd., of China
Hobby Toy Hammer Ball setsThe toy sets contain small balls that violate regulations for toys intended for children under three years of age because they are a choking hazard and can cause serious injury or death.
- Unclassified
Consumer Product Recall · June 5, 2025
GD Midea Air-Conditioning Equipment Co. Ltd., of China
U and U+ Window Air ConditionersPooled water in the air conditioners can fail to drain quickly enough, which can lead to mold growth. Mold exposure poses risks of respiratory issues or other infections to some consumers.
- Unclassified
- Unclassified
Consumer Product Recall · June 5, 2025
Yamaha Motor Corporation U.S.A., of Cypress, California
Yamaha Golf Car VehiclesThe accelerator pedal spring can fail to return to idle when a consumer stops pressing the accelerator pedal, posing a crash hazard.
- Unclassified
Consumer Product Recall · June 5, 2025
Rinnai America Corporation, of Peachtree City, Georgia
Rinnai i-Series Plus gas boilersThe boiler door can fail to seal properly due to incorrect screws, allowing carbon monoxide (CO) gases to escape, posing a carbon monoxide poisoning hazard.
- Unclassified
Consumer Product Recall · June 5, 2025
Nanjing Dengfengda Trading Co. Ltd., d/b/a DFD Trading, of China
ZHORANGE Portable BassinetsThe recalled portable bassinets violate the federal safety standard for Infant Sleep Products because the sides are too low to contain the infant and the portable bassinets do not have a stand, posing a fall hazard. These violations create an unsafe sleeping environment for infants.
- Unclassified
Consumer Product Recall · June 5, 2025
Fuzhouwanhonggongyipinyouxiangongsi, dba ZRWD, of China
ZRWD Infant SwingsThe swings pose a deadly suffocation risk because they were marketed for infant sleep and they have an incline angle greater than 10 degrees, in violation of the CPSC's Infant Sleep Products Standard and Safe Sleep for Babies Act. The swings also fail to meet mandatory warning requirements under the swing standard. In addition, the remote control for the swing contains a lithium coin battery and the products are missing the required warnings and instructions for consumer products containing button cell and coin batteries under Reese's Law. When button cell or coin batteries are swallowed, the ingested batteries can cause serious injuries, internal chemical burns and death.
- Class II
Medical Device Recall · June 4, 2025
Siemens Medical Solutions USA, Inc
UROSKOP Omnia. Model Number: 10094910A resistor in the frequency inverter may strongly overheat potentially igniting the plastic housing of the frequency inverter on fire.
- Class II
Medical Device Recall · June 4, 2025
Siemens Healthcare Diagnostics, Inc.
ADVIA¿ 120/2120/2120i 3-in-1 TESTpoint Control (ABN2 Control)Products have the incorrect platelet (PLT) value assignments for the ADVIA 120/2120/2120i Hematology Systems.
- Class III
Medical Device Recall · June 4, 2025
Brand Name: T4 Total ELISA Product Name: T4 Total ELISA Model/Catalog Number: EIA-4568 Product Description: T4 Total ELISAAn incoming complaint reported that the expiration date on the kit box label and Certificate of Analysis (CoA) exceeded the shelf life of the standards and control solutions in the kit by 2 months (i.e., 2026-03-31 instead of 2026-01-31). The expiration dates on the bottle labels were correct (i.e., 2026-01-31).
- Class II
Medical Device Recall · June 4, 2025
Siemens Healthcare Diagnostics, Inc.
ADVIA¿ 120/2120/2120i 3-in-1 TESTpoint Control (ABN1 Control)Products have the incorrect platelet (PLT) value assignments for the ADVIA 120/2120/2120i Hematology Systems.
- Class II
Medical Device Recall · June 4, 2025
Siemens Healthcare Diagnostics, Inc.
ADVIA¿ 120/2120/2120i 3-in-1 TESTpoint Control (Norm Control)Products have the incorrect platelet (PLT) value assignments for the ADVIA 120/2120/2120i Hematology Systems.
- Class II
Medical Device Recall · June 4, 2025
Siemens Medical Solutions USA, Inc
UROSKOP Omnia Max. Model Number: 10762473A resistor in the frequency inverter may strongly overheat potentially igniting the plastic housing of the frequency inverter on fire.
- Class II
Medical Device Recall · June 4, 2025
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Azurion 7 M20. Fluoroscopic X-Ray System.Potential for bolts connecting the gearbox to the mounting flange of the C-arm to become loose.
- Class II
Medical Device Recall · June 4, 2025
Siemens Healthcare Diagnostics, Inc.
ADVIA¿ 120/2120/2120i SETpoint CalibratorProducts have the incorrect platelet (PLT) value assignments for the ADVIA 120/2120/2120i Hematology Systems.
- Class III
Medical Device Recall · June 4, 2025
Zvu Anorectal Manometry Procedure Kit, REF: HRAM-PROC-10Anorectal manometry procedure kit outer kit label is mislabeled with an incorrect expiration date; the manufacturing date was used in place of the expiration date. All inner labels on kit components display the correct expiration date.
- Class I
Food Recall · June 4, 2025
Bornstein Frozen Shrimp Meat, Wild Caught - Product of USA. Product is cooked and Ready-To-Eat. Processed in the USA by Bornstein Seafoods Inc. Astoria, OR. The following items are being recalled: ZThe recall was the result of the firm's routine sampling program and Listeria monocytogenes was detected in an in-process shrimp sample in a food production environment.
- Unclassified
Vehicle Recall · June 3, 2025
2024 KAWASAKI NINJA 500A broken clutch release lever may not disengage, disabling the motorcycle and increasing the risk of a crash.
- Class II
Medical Device Recall · June 3, 2025
BD Heyman Follower Coude Tip for following sizes: 12Fr - REF:021312 14Fr - REF:021314, 16Fr - REF: 021316Cather packaging may contain the incorrect French size.
- Class I
Medical Device Recall · June 3, 2025
Hamilton C6 REF 160021 (ESM Board PN 10144626 UDI-DI code: 76300028PN160021ZW Hamilton C6 is a ventilator intended to provide positive pressure ventilatory support to adults and pediatrics and optA mechanical defect on a printed circuit board (PCB) as a result of PCB separating process. This defect might cause the ventilator to either fail at startup (no patient involvement) or during the use of the device enter ambient state, resulting in an interruption of ventilation.
- Class II
Medical Device Recall · June 3, 2025
SwabCap Disinfecting Cap for Needlefree Connectors: SwabSleeve, REF: SCXT3-5-2000; SwabCap, 200-ct. Box, REF: SCXT3-2000Due to a manufacturing issue, disinfecting cap for needle-free connectors may have an incomplete seal between the foil lid and plastic container, which may result in isopropyl alcohol evaporation from the sponge, which may result in inadequate disinfection.
- Class II
Medical Device Recall · June 3, 2025
Becton, Dickinson and Company, BD Bio Sciences
REF: 666289 , BD FACS, 7-Color Setup Beads, 25 Runs, CE, IVD. Used in flow cytometry for fluorescence compensation.Due to customer complaints, errors in spectral overlap factors table for 7-color setup beads may affect accurate setup of the flow cytometry instrument prior to analyzing samples.
- Unclassified
Vehicle Recall · June 3, 2025
Ineos Automotive Americas, LLC
2024 INEOS GRENADIERAn unlatched door can open unexpectedly while the vehicle is in motion, increasing the risk of injury.
- Class II
Food Recall · June 3, 2025
Peak Cocktails Blood Orange Spritz 8.4 fl oz aluminum cans sold as an individual flavor and in variety packs of 12, 24, and 48 cans. Batch Codes: B25127, B25128; Packaging Date: 05/07/2025, 05/08/20Overpressurization leading to exploding cans
- Class II
Medical Device Recall · June 3, 2025
REF: 123400,Bard Urologist's Tray, For the Obstructed UrethraCather packaging may contain the incorrect French size.
- Class I
Medical Device Recall · June 3, 2025
Bravo CF capsule delivery device, designed to place and attach a pH monitoring capsule to the esophagus using endoscopic or manometric guidance, Product Number FGS-0635 (5 pack) and FGS-0636 (1 pack)It has been determined that misapplied adhesive on the Bravo CF capsule delivery device may lead to its malfunction. Specifically, the misapplied adhesive may prevent the capsule from attaching to the patient's esophagus or detaching from the delivery device.
- Class II
Medical Device Recall · June 3, 2025
BD Heyman Follower Straight Tip for following sizes: 10Fr - REF:21110, 12Fr - REF:21112, 14Fr - REF: 21114, 20Fr - REF: 21120Cather packaging may contain the incorrect French size.
- Class II
Medical Device Recall · June 3, 2025
Becton, Dickinson and Company, BD Bio Sciences
REF: 335775 , BD FACS, 7-Color Setup Beads, 25 setups per kit, Rx Only, IVD. Used in flow cytometry for fluorescence compensation.Due to customer complaints, errors in spectral overlap factors table for 7-color setup beads may affect accurate setup of the flow cytometry instrument prior to analyzing samples.
- Unclassified
Vehicle Recall · June 2, 2025
Toyota Motor Engineering & Manufacturing
2025 TOYOTA CAMRY HYBRIDA damaged seat belt may not adequately restrain an occupant, increasing the risk of injury during a crash.
- Class II
Drug Recall · June 2, 2025
KETAmine Hydrochloride Injection, USP, 50 mg/5mL (10 mg/mL), For IM Use or Slow IV Use, 5 mL Sterile Single-Dose Vial, Rx Only, For Office Use Only, Compounded Durg by: Medivant Healthcare, 158 S. KyrLack of Assurance of Sterility: A recent FDA inspection revealed concerns with the sterile manufacturing process.
- Unclassified
Vehicle Recall · June 2, 2025
2025 HYUNDAI IONIQ 5Reduced braking performance can increase the distance required to stop the vehicle, increasing the risk of a crash.