PlainRecalls

2024 Recalls

6,210 recalls · Page 64 of 125

2024 Recall Year Insight

Federal agencies issued 6,210 product recalls indexed by PlainRecalls in calendar year 2024. That represents about 6.11% of the 101,704 total recalls we track from 1995 through the present, and averages roughly 17.0 recalls per day across the FDA, CPSC, and NHTSA combined. Year-level views are the cleanest way to see macro patterns: volume spikes often correlate with new regulatory priorities (e.g., infant-sleep products after 2021, lithium-ion batteries after 2022), supply-chain contamination events, or changes in agency enforcement intensity, while quiet years can reflect either genuine product-safety improvements or reduced agency staffing and reporting lag. With 125 pages at 50 recalls each, browsing this year end-to-end gives a statistically representative sample of what the federal recall pipeline looked like in 2024.

On this page of 50 records, severity classification shows 17 critical, 33 moderate, and 0 lower-severity recalls. The page references 24 distinct recalling firms operating in 5 distinct product categories, with 36 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Devices (27), NHTSA (14), CPSC (9), which matters because each agency's recall authority, hazard framing, and remedy mechanism differ, an FDA food recall, a CPSC consumer-product recall, and a NHTSA vehicle recall are legally distinct instruments even when the underlying hazard language sounds similar. Reviewing the dominant agency for a given year is one of the fastest ways to understand where federal attention was concentrated.

Year-indexed browsing serves three practical purposes: historical research (tracking how a hazard class evolved over time), consumer action (finding whether a product purchased in 2024 was later recalled), and journalistic or regulatory context (understanding what the enforcement landscape looked like in a given period). Every record on this page links to a full detail view with the hazard, remedy, distribution, and agency-assigned recall number, always use that recall number to verify current status directly with the issuing agency before acting on time-sensitive remedies, because agencies amend, terminate, and expand recalls in the months and years after initial publication. Data on this page reflects federal agency public filings; the agency's live record remains authoritative for legal, medical, or safety decisions. Verify with FDA openFDA, CPSC, or NHTSA for the system-of-record on any specific recall. PlainRecalls indexes this archive for research and consumer awareness purposes.

FDA Devices Critical Jul 3, 2024

SENSE XL TORSO COIL 3.0T. 16-element receive only coil for torso and abdomen imaging in Philips MR Intera and Achieva Systems. Model Numbers: 4535673…

Philips North America Llc

FDA Devices Moderate Jul 3, 2024

EVERA S VR, Model Number DVBC3D1, Implantable Cardioverter Defibrillator

Medtronic Inc.

FDA Devices Moderate Jul 3, 2024

AXIOM MULTIX MP - Inended Radiographic X ray Table is a patient table used in conjunction with the Siemens Multix PRO and TOP Systems radiographic d…

Siemens Medical Solutions USA, Inc

FDA Devices Moderate Jul 3, 2024

MULTIX TOP - Intended Use: The Multix TOP I PRO Radiographic X ray Table is a patient table used in conjunction with the Siemens Multix PRO and TOP S…

Siemens Medical Solutions USA, Inc

FDA Devices Moderate Jul 3, 2024

Accu-Chek Guide (SC) Kit -Intended to quantitatively measure glucose in fresh capillary whole blood from the fingertip, palm, and upper arm as an aid…

Roche Diabetes Care, Inc.

FDA Devices Moderate Jul 3, 2024

AXIOM MULTIX MP - Intended Radiographic X ray Table is a patient table used in conjunction with the Siemens Multix PRO and TOP Systems radiographic …

Siemens Medical Solutions USA, Inc

FDA Devices Moderate Jul 3, 2024

Product not distributed in the US. Implantable Cardioverter Defibrillators: a. VIVA QUAD XT CRT-D, Model Number DTBA2QQ. b. CLARIA MRI CRT-D…

Medtronic Inc.

FDA Devices Moderate Jul 3, 2024

COBALT XT HF QUAD CRT-D MRI SureScan, Model Number DTPA2QQ, Implantable Cardioverter Defibrillator

Medtronic Inc.

FDA Devices Moderate Jul 3, 2024

RingLoc Bi-Polar Hip System Acetabular Cup, 41 mm Outer Diameter - Used in hip hemi-arthroplasty Item Number: 11-165206

Biomet, Inc.

FDA Devices Moderate Jul 3, 2024

CROME HF QUAD CRT-D MRI SureScan, Model Number DTPC2QQ, Implantable Cardioverter Defibrillator

Medtronic Inc.

FDA Devices Moderate Jul 3, 2024

AXIOM Vertix Solitaire - The Vertix MD Trauma has been specially designed for examining emergency and accident patients as well as for use in outpat…

Siemens Medical Solutions USA, Inc

FDA Devices Moderate Jul 3, 2024

Cobalt XT HF CDT-D MRI SureScan, Model Number: DTPA2D4, Implantable Cardioverter Defibrillator

Medtronic Inc.

FDA Devices Moderate Jul 3, 2024

CARESCAPE Canvas Smart Display, Model Numbers: a) 5700023, b) 5700023-02, c) 5939590-102; monitor, physiological, patient

GE Healthcare Finland Oy

FDA Devices Moderate Jul 3, 2024

AXIOM MULTIX MT - Intended Radiographic X ray Table is a patient table used in conjunction with the Siemens Multix PRO and TOP Systems radiographic …

Siemens Medical Solutions USA, Inc

FDA Devices Moderate Jul 3, 2024

Titan Blis-Sonic Scaler packaged with the Titan Scaler Tip - Perio (part number 261669) (1) P/N 264563 (2) P/N 264565 The scaler tip is used wi…

Dental EZ Group Star Dental Division

FDA Devices Moderate Jul 3, 2024

EVERA MRI S DR SureScan, Model Number DDMC3D4, Implantable Cardioverter Defibrillator

Medtronic Inc.

FDA Devices Moderate Jul 3, 2024

AXIOM MULTIX MT - Intended Radiographic X ray Table is a patient table used in conjunction with the Siemens Multix PRO and TOP Systems radiographic d…

Siemens Medical Solutions USA, Inc

FDA Devices Moderate Jul 3, 2024

ZE for Vertix Solitaire - The AXIOM Vertix Solitaire is a component and has been specially designed for examining emergency and accident patients as …

Siemens Medical Solutions USA, Inc

FDA Devices Moderate Jul 3, 2024

PRIMO MRI VR SureScan, Model Number DVMD3D4, Implantable Cardioverter Defibrillator

Medtronic Inc.

FDA Devices Critical Jul 3, 2024

Inspire Model 3028, IV Implantable Pulse Generator

Inspire Medical Systems Inc.

FDA Devices Moderate Jul 3, 2024

The VASOVIEW HemoPro Endoscopic Vessel Harvesting Systems are designed for use in conjunction with the 7 mm Extended Length Endoscope. The Harvesting…

Maquet Cardiovascular, LLC

FDA Devices Moderate Jul 3, 2024

COBALT XT HF QUAD CRT-D MRI SureScan, Model Number DTPA2Q1, Implantable Cardioverter Defibrillator

Medtronic Inc.

FDA Devices Moderate Jul 3, 2024

Ultrathane Mac-Loc Locking Loop Multipurpose Drainage Catheter ULT16.0-38-25-P-6S-MCL-HC--Intended for percutaneous drainage in a variety of drainage…

Cook Incorporated

FDA Devices Critical Jul 3, 2024

SENSE XL TORSO COIL 1.5T Mk2. 16-element receive only coil for torso and abdomen imaging in Philips MR Intera and Achieva Systems. Model Numbers: 45…

Philips North America Llc

FDA Devices Moderate Jul 3, 2024

MIRRO MRI DR SureScan, Model Number DDME3D1, Implantable Cardioverter Defibrillator

Medtronic Inc.

FDA Devices Moderate Jul 3, 2024

Ultrathane Cook-Cope Type Locking Loop Multipurpose Drainage Catheter-ULT12.0-38-45-P-6S-CLM-RH-ntended for percutaneous drainage in a variety of dra…

Cook Incorporated

FDA Devices Moderate Jul 3, 2024

EVERA MRI S DR SureScan, Model Number DDMC3D1, Implantable Cardioverter Defibrillator

Medtronic Inc.

CPSC Moderate Jul 3, 2024

American Honda Motor Recalls Off-Road Motorcycles Due to Crash and Injury Hazards

CPSC Moderate Jul 3, 2024

Focusee Recalls Tideway Hair Dryers Due to Electrocution or Shock Hazard

CPSC Moderate Jul 3, 2024

Hatch Baby Recalls Power Adapters Sold with Rest 1st Generation Sound Machines Due to Shock Hazard

CPSC Moderate Jul 3, 2024

SWOMOG Children's Pajamas Recalled Due to Burn Hazard; Violation of Federal Flammability Regulations; Sold Exclusively on Amazon.com by SWOMOG

NHTSA Critical Jul 3, 2024

BMW 2006-2012: AIR BAGS:FRONTAL:DRIVER SIDE:INFLATOR MODULE

BMW

NHTSA Critical Jul 3, 2024

ALFA ROMEO 2017-2024: EQUIPMENT:OTHER:LABELS

ALFA ROMEO

NHTSA Critical Jul 3, 2024

ALFA ROMEO,FIAT,JEEP 2017-2024: AIR BAGS:FRONTAL

ALFA ROMEO,FIAT,JEEP

NHTSA Critical Jul 3, 2024

FREIGHTLINER,WESTERN STAR 2025: STEERING:LINKAGES:TIE ROD ASSEMBLY

FREIGHTLINER,WESTERN STAR

NHTSA Critical Jul 2, 2024

HONDA 2024: TIRES:MARKINGS

HONDA

NHTSA Critical Jul 2, 2024

FISKER 2023: ELECTRICAL SYSTEM:PROPULSION SYSTEM:TRACTION BATTERY:MANAGEMENT SYSTEM/ENERGY CONTROL MODULE (BMS/BECM)

FISKER

NHTSA Critical Jul 1, 2024

NISSAN 2024: VISIBILITY:WINDSHIELD

NISSAN

NHTSA Critical Jul 1, 2024

LUCID 2022-2023: ELECTRICAL SYSTEM:PROPULSION SYSTEM:TRACTION BATTERY THERMAL:MANAGEMENT:SOFTWARE

LUCID

NHTSA Critical Jun 28, 2024

FORD 2024: SERVICE BRAKES, HYDRAULIC:BRAKE FLUID LOW WARNING:SWITCH/SENSOR/FLOAT

FORD

NHTSA Critical Jun 28, 2024

LUCID 2022-2024: VISIBILITY:DEFROSTER/DEFOGGER/HVAC SYSTEM

LUCID

NHTSA Critical Jun 28, 2024

FORD 2022-2023: STEERING:ELECTRIC POWER ASSIST SYSTEM

FORD

NHTSA Critical Jun 28, 2024

CHEVROLET,GMC 2024: FUEL SYSTEM, GASOLINE:STORAGE:TANK ASSEMBLY

CHEVROLET,GMC

NHTSA Critical Jun 28, 2024

CHEVROLET 2024: SUSPENSION:FRONT:CONTROL ARM:LOWER ARM

CHEVROLET

NHTSA Critical Jun 28, 2024

FORD 2024: VISIBILITY:WINDSHIELD

FORD

CPSC Moderate Jun 27, 2024

At Home Procurement Recalls Toy Trunk Storage Chests Due to Entrapment and Suffocation Hazards

CPSC Moderate Jun 27, 2024

Baseus Magnetic Wireless Charging Power Banks Recalled Due to Fire Hazard; Imported by Shenzhen Baseus Technology

CPSC Moderate Jun 27, 2024

Daikin Comfort Technologies Manufacturing Recalls Daikin FIT, Amana Brand S-series, and Goodman SD Heat Pumps Due to Risk of Excessive Heat Exposure

Daikin Comfort Technologies Manufacturing L.P., of Houston, Texas

CPSC Moderate Jun 27, 2024

Dania Furniture Recalls Hayden Bookcase Due to Tip-Over and Entrapment Hazards; 4-Year-Old Child Died from Tip-Over (Recall Alert)

Dania Furniture, of Boise, Idaho

CPSC Moderate Jun 27, 2024

REI Recalls Co-op Cycles REV Children's Bicycles with Training Wheels Due to Fall and Injury Hazards

RECREATIONAL EQUIPMENT INC. (REI), of Sumner, Washington

Nearby Recall Years

Browse recalls from adjacent calendar years to see how federal enforcement volume has shifted over time.

Compare 2024 with 2023 →

Data Sources

  • Source: FDA openFDA Enforcement API - calendar-year recall filings for food, drugs, and devices
  • Source: CPSC + NHTSA - consumer product and vehicle recall feeds for 2024

Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. Figures cover calendar year 2024 across the FDA, CPSC and NHTSA federal recall feeds. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of August 2026.