PlainRecalls

2024 Recalls

6,210 recalls · Page 120 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 12 critical, 37 moderate, and 1 lower-severity recalls. The page references 26 distinct recalling firms operating in 4 distinct product categories, with 45 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Devices (39), NHTSA (5), CPSC (3), 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 Moderate Jan 24, 2024

Calibration Serum Level 3 - IVD For use as a Calibrator in clinical chemistry assays Catalog Number: CAL2351

Randox Laboratories Ltd.

FDA Devices Moderate Jan 24, 2024

Ultrasound EA (Ergonomic Advantage) table versions; G3 Multi-Specialty Echocardiography and Multi-Specialty with Electric Access Back Supports [left …

Oakworks Inc

FDA Devices Moderate Jan 24, 2024

Maquet Equipment OR Light Systems, Model Numbers and Catalog Numbers BRAINLAB CAMERA - ARDEQT269000A, BRAINLAB CAMERA - ARDEQT269000C, BRAINLAB CAMER…

Getinge Usa Sales Inc

FDA Devices Moderate Jan 24, 2024

Maquet Volista, Volista Access, Volista Access II, Volista Standop OR Light System, Model Numbers and Catalog Numbers ROL B FOR VLT400SF STP - ARDROL…

Getinge Usa Sales Inc

FDA Devices Moderate Jan 24, 2024

Maquet Hanaulux HLX3000 OR Light Systems, Model Numbers and Catalog Numbers H3 BC - HM567811111C

Getinge Usa Sales Inc

FDA Devices Critical Jan 24, 2024

Product REF 4050-100N, DRAIN, EXPRESS BRU W/AC, Blood Recovery Unit

Maquet Cardiovascular, LLC

FDA Devices Moderate Jan 24, 2024

Calibration Serum Level 3 CAL2351

Randox Laboratories Ltd.

FDA Devices Moderate Jan 24, 2024

Maquet G8 / G8E OR Light Systems, Model Numbers and Catalog Numbers G8 LC E - ARD568131211C, G8G8 DF E - ARD568121111C, G8G8FS DF - ARD568121131C

Getinge Usa Sales Inc

FDA Devices Moderate Jan 24, 2024

Maquet Axcel / Axcel + OR Light Systems, Model Numbers and Catalog Numbers AXL 5001 - ARD567501961C, AXL 5001S - ARD567505961C, AXL 5002 - ARD5675019…

Getinge Usa Sales Inc

FDA Devices Moderate Jan 24, 2024

Maquet Hanaulux HLX2000 OR Light Systems, Model Numbers and Catalog Numbers 3001 - ARD567424001C, 3001 HMS07 - ARD567722001C, 3001 HXS12 - ARD5677030…

Getinge Usa Sales Inc

FDA Devices Moderate Jan 24, 2024

Maquet Hanaulux 2006/ 2007, Blue 100, Blue 130/ 90, Blue Series 30/ 80, and Prismatic OR Light Systems. No Model Numbers.

Getinge Usa Sales Inc

FDA Devices Moderate Jan 24, 2024

HIGH PRESSURE ROTATOR WITH FEMALE LUER LOCK, List Number MX497HP

Smiths Medical Asd Inc

FDA Devices Moderate Jan 24, 2024

SOLTIVE SuperPulsed Laser Fibers, Model No. TFL-FBX200BS

Olympus Corporation of the Americas

FDA Devices Moderate Jan 24, 2024

Maquet XTen OR Light Systems, Model Numbers and Catalog Numbers 3001 HMD14 - ARD567732001C, X TEN DUO - ARD568221510C, X TEN DUO - ARD568221561C, X10…

Getinge Usa Sales Inc

FDA Devices Critical Jan 24, 2024

regard Operative LAP, Item Number 800943001; surgical convenience kit

ROi CPS LLC

FDA Devices Critical Jan 24, 2024

Distal Phasitron, Part: S20020, for use with Percussionaire VDR-4 control driver (or control unit)

Percussionaire Corporation

FDA Devices Moderate Jan 24, 2024

(1) CareEvent, Model No. 866435 (2) CareEvent Upgrade, Model no. 866436

Philips North America

FDA Devices Critical Jan 24, 2024

Product REF 4000-100N, DRAIN, EXPRESS SINGLE W/AC, Single Collection

Maquet Cardiovascular, LLC

FDA Devices Moderate Jan 24, 2024

Maquet Prismalix OR Light Systems, Model Numbers and Catalog Numbers 3001 - ARD567424001C, 3001 HMS07 - ARD567722001C, 3001 HXS12 - ARD567703001C, 40…

Getinge Usa Sales Inc

FDA Devices Moderate Jan 24, 2024

Ultrasound EA (Ergonomic Advantage) table versions; G3 (General 3 Section) Echocardiography -An Ultrasound examination table

Oakworks Inc

FDA Devices Moderate Jan 24, 2024

Ultrasound EA (Ergonomic Advantage) table version; V2 (Vascular 2 Section) Echocardiography -An Ultrasound examination table

Oakworks Inc

FDA Devices Moderate Jan 24, 2024

6IN PRESSURE TUBING, List Number MX20617

Smiths Medical Asd Inc

FDA Devices Moderate Jan 24, 2024

Vasoview Hemopro Endoscopic Vessel Harvesting System, model VH-3500.

Maquet Cardiovascular, LLC

FDA Devices Critical Jan 24, 2024

ExcelsiusGPS Flat Panel Fluoroscopy Fixture Kit, Part number 6203.2100

Globus Medical, Inc.

FDA Devices Moderate Jan 24, 2024

GammaPod - Treatment Planning System-a component of the GammaPod Irradiation System. Ref: XMSGP030A09.07-0.01 Intended for use in the noninvasiv…

Xcision Medical Systems, LLC

FDA Devices Moderate Jan 24, 2024

PRIMA TT Glenoid Monoblock/Modular reverse TT baseplates: Description/Product Code: BASEPLATE D.25MM REGULAR/1975.14.500, BASEPLATE D.28MM REGULAR/…

Limacorporate S.p.A

FDA Devices Moderate Jan 24, 2024

Curaplex Field Cric Kit with ET Tube, Item Number 36611. The kit provides healthcare professionals with an assortment of supplies to perform a crico…

Sarnova HC, Llc

FDA Devices Moderate Jan 24, 2024

INDICAID COVID-19 Rapid Antigen At-Home Test, REF: P0040

PHASE SCIENTIFIC INTERNATIONAL LIMITED

FDA Devices Moderate Jan 24, 2024

Medex LOGICAL CATH LAB KIT, List Number M20754

Smiths Medical Asd Inc

FDA Devices Moderate Jan 24, 2024

Soltive SuperPulsed Laser System TFL FIBER CLEAVER, Model Number TFL-AFC

Olympus Corporation of the Americas

FDA Devices Moderate Jan 24, 2024

20IN (50.8CM) BRAIDED INJ LINE, ROTATING ADAPT, List Number MX682BR

Smiths Medical Asd Inc

FDA Devices Moderate Jan 24, 2024

Calibration Serum Level 3. CAL 3, REF CAL2351. Human Assayed Multi-Sera Level 2 (HN1530) Human Assayed Multi-Sera Level 3 (HE 1532)

Randox Laboratories Ltd.

FDA Devices Moderate Jan 24, 2024

Spectral CT 7500, Software Version 5.0.0.X. Computed Tomography X-Ray System.

Philips North America Llc

FDA Devices Moderate Jan 24, 2024

Maquet Orchide OR Light Systems, Model Numbers and Catalog Numbers OHDII FHD QL VP01 - ARD568803935, OHDII FHD QL AIR03 U - ARD568803952, OHDII FHD Q…

Getinge Usa Sales Inc

FDA Devices Moderate Jan 24, 2024

Medex 700PSI STOPCOCK W/ROTATOR, List Number MX4331R

Smiths Medical Asd Inc

FDA Devices Moderate Jan 24, 2024

Ultrasound EA (Ergonomic Advantage) table versions; G2 (GENERAL 2) -An Ultrasound examination table

Oakworks Inc

FDA Devices Moderate Jan 24, 2024

TECNIS Toric II OptiBlue IOL Models ZCW

Johnson & Johnson Surgical Vision, Inc.

FDA Devices Moderate Jan 24, 2024

PosiFlush Prefilled Saline Syringe with General Pump Compatibility (10mL Syringe with 10mL Saline Fill), Catalog Number 306547

Becton Dickinson & Company

FDA Devices Moderate Jan 24, 2024

FreeStyle Libre 3 App, part of Continuous Glucose Monitoring System, when used on the Android 13 Operating System

Abbott Diabetes Care, Inc.

NHTSA Critical Jan 22, 2024

TESLA 2023: BACK OVER PREVENTION: SENSING SYSTEM: CAMERA

TESLA

NHTSA Critical Jan 19, 2024

FORD 2011-2019: STRUCTURE:BODY:ROOF AND PILLARS

FORD

CPSC Moderate Jan 18, 2024

Bokser Home Recalls Mattress Pads Due to Fire Hazard and Violation of Federal Mattress Pad Flammability Regulation

Anhui Zhongqinghonyu Home Textile Technology Co. LTD, of China

CPSC Moderate Jan 18, 2024

Home Design Recalls Upholstered Low Profile Standard and Platform Beds Due to Fall and Injury Hazards

CPSC Moderate Jan 18, 2024

Steamist Recalls Wall-Mounted Tilt-Up Bath & Shower Seats Due to Fall and Laceration Hazards

NHTSA Critical Jan 18, 2024

KIA 2022-2024: STRUCTURE:BODY:ROOF AND PILLARS

KIA

NHTSA Critical Jan 18, 2024

LAND ROVER 2018-2022: BACK OVER PREVENTION: SENSING SYSTEM: CAMERA

LAND ROVER

NHTSA Critical Jan 18, 2024

MAZDA 2024: STEERING

MAZDA

FDA Food Critical Jan 17, 2024

Chocolate Walnut Fudge, 8oz, packaged in clear, plastic clamshell.

Valley View Candies dba

FDA Food Critical Jan 17, 2024

Peanut Butter Fudge, 8oz, packaged in clear, plastic clamshell.

Valley View Candies dba

FDA Food Low Jan 17, 2024

Brand Name: SUPREX Plant Based Nutrition. Product Name: Carb & Sugar Block. Product Size: 120 Vegetable Cellulose Capsules per bottle. Container des…

Vita 360, LLC

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.