PlainRecalls

2024 Recalls

4,937 recalls · Page 88 of 99

2024 Recall Year Insight

Federal agencies issued 4,937 product recalls indexed by PlainRecalls in calendar year 2024. That represents about 5.88% of the 83,949 total recalls we track from 1995 through the present, and averages roughly 13.5 recalls per day across the FDA, CPSC, NHTSA, and USDA FSIS 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 99 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 16 critical, 34 moderate, and 0 lower-severity recalls. The page references 24 distinct recalling firms operating in 5 distinct product categories, with 35 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Devices (38), NHTSA (8), CPSC (4), 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, NHTSA, or USDA FSIS for the system-of-record on any specific recall. PlainRecalls indexes this archive for research and consumer awareness purposes.

FDA Devices Critical Feb 14, 2024

BrightView XCT, gamma camera for SPECT; Model Nos.: 6-digit format 882482; 12-digit format 453560462131 453560749161

Philips North America

FDA Devices Moderate Feb 14, 2024

BD BBL Sensi Disc Meropenem- 10 ug, used for semi-quantitative in vitro susceptibility testing. Catalog Number 231703 and 231704¿

Becton Dickinson & Co.

FDA Devices Moderate Feb 14, 2024

HRIS ACET CUP CUT TIP 26X140 Part Number: 6210-5-100. single-use, sterile surgical instruments used during hip arthroplasty

Howmedica Osteonics Corp.

FDA Devices Moderate Feb 14, 2024

BD BBL Sensi Disc Ceftaroline - 30 ug, used for semi-quantitative in vitro susceptibility testing. Catalog Number 232231¿

Becton Dickinson & Co.

FDA Devices Moderate Feb 14, 2024

BD BBL Sensi Disc Cefepime - 30 ug¿, used for semi-quantitative in vitro susceptibility testing. Catalog Number 231696¿

Becton Dickinson & Co.

FDA Devices Moderate Feb 14, 2024

BD BBL Sensi Disc Imipenem- 10 ug, used for semi-quantitative in vitro susceptibility testing. Catalog Number 231644 and 231645¿

Becton Dickinson & Co.

FDA Devices Critical Feb 14, 2024

1. HeartMate Touch Communication System, REF HMT1100 2. HeartMate Touch Communication System, Rental REF HMT1100-R 3. HeartMate Touch Communication…

Thoratec Corp.

FDA Devices Moderate Feb 14, 2024

Globus Medical Cranial Drill, 6.00mm - instruments for access, preparation, and placement of cranial devices with the ExcelsiusGPS. Ref: 6143.1…

Globus Medical, Inc.

FDA Devices Moderate Feb 14, 2024

BD BBL Sensi Disc Moxifloxacin- 5 ug, used for semi-quantitative in vitro susceptibility testing. Catalog Number 231758¿

Becton Dickinson & Co.

FDA Devices Moderate Feb 14, 2024

BD BBL Sensi Disc Chloramphenicol- 30 ug, used for semi-quantitative in vitro susceptibility testing. Catalog Number 230733¿and 231274¿

Becton Dickinson & Co.

FDA Devices Moderate Feb 14, 2024

Ingenia 1.5T (Product Number 781396) - HA FlexTrak II (Accessory Number 989710008732), patient transportation system

Philips North America

FDA Devices Moderate Feb 14, 2024

Flow-i C20 Anesthesia System, model 6677200

Getinge Usa Sales Inc

FDA Devices Moderate Feb 14, 2024

Globus Medical Cranial Drill with Stop, 2.40mm - Instruments for access, preparation, and placement of cranial devices with the ExcelsiusGPS. Ref : …

Globus Medical, Inc.

FDA Devices Moderate Feb 14, 2024

BD BBL Sensi Disc Ertapenem- 10 ug, used for semi-quantitative in vitro susceptibility testing. Catalog Number 232174 and 232175¿

Becton Dickinson & Co.

FDA Devices Critical Feb 14, 2024

Cardinal Health Monoject, 6ML Enteral Syringe (purple) Low Dose (LDT) - For Use with ENFit Connection System, REF 406SE

Cardinal Health 200, LLC

FDA Devices Critical Feb 14, 2024

BrightView X, gamma camera for SPECT; Model Nos.: 6-digit format 882478; 12-digit format 453560824741 453560829261;

Philips North America

FDA Devices Moderate Feb 14, 2024

Bubble Sensor (REF: 70105.5720)

Maquet Medical Systems USA

FDA Devices Moderate Feb 14, 2024

Flow-e Anesthesia System, model 6887900

Getinge Usa Sales Inc

FDA Devices Critical Feb 14, 2024

Cardinal Health Monoject, 3 mL Syringe Luer-Lock Tip Soft Pack, REF 1180300777

Cardinal Health 200, LLC

FDA Devices Critical Feb 14, 2024

Cardinal Health Monoject, 1 mL Tuberculin Syringe Luer-Lock Tip Soft Pack, REF 1180100777

Cardinal Health 200, LLC

FDA Devices Critical Feb 14, 2024

Cardinal Health Monoject, 12mL Enteral Syringe (purple) For Use with ENFit Connection System, REF 412SE

Cardinal Health 200, LLC

FDA Devices Moderate Feb 14, 2024

BD BBL Sensi Disc Ciprofloxacin- 5 ug, used for semi-quantitative in vitro susceptibility testing. Catalog Number 231657¿and 231658¿

Becton Dickinson & Co.

FDA Devices Moderate Feb 14, 2024

BD BBL Sensi Disc Aztreonam - 30 ug¿, used for semi-quantitative in vitro susceptibility testing. Catalog Numbers 231640¿and 231641.

Becton Dickinson & Co.

FDA Devices Moderate Feb 14, 2024

FLEXSelect 5/16" Amber Latex Elastics-Intended use is orthodontics, braces, tooth gap, Ref: AMD56

G & H Wire Company

FDA Devices Moderate Feb 14, 2024

Barco MDSC-8527 NXF, Part Number K9352421

Barco N.V.

FDA Devices Moderate Feb 14, 2024

BD BBL Sensi Disc Levofloxacin- 5 ug, used for semi-quantitative in vitro susceptibility testing. Catalog Number 231705 and 231706¿

Becton Dickinson & Co.

FDA Devices Moderate Feb 14, 2024

BD BBL Sensi Disc Augmentin - 3¿g, Catalog Number 291270¿used for semi-quantitative in vitro susceptibility testing.

Becton Dickinson & Co.

FDA Devices Moderate Feb 14, 2024

BD BBL Sensi Disc Sulfamethoxazole with Trimethoprim 23.75/1.25 ug, used for semi-quantitative in vitro susceptibility testing. Catalog Number 231536…

Becton Dickinson & Co.

FDA Devices Moderate Feb 14, 2024

BD BBL Sensi Disc Ceftazidime- 30 ug, used for semi-quantitative in vitro susceptibility testing. Catalog Number 231632¿and 231633¿

Becton Dickinson & Co.

FDA Devices Moderate Feb 14, 2024

Globus Medical Cranial Drill with Stop, 3.20mm - instruments for access, preparation, and placement of cranial devices with the ExcelsiusGPS. Ref: …

Globus Medical, Inc.

FDA Devices Moderate Feb 14, 2024

BD BBL Sensi Disc Ofloxacin- 5 ug, used for semi-quantitative in vitro susceptibility testing. Catalog Number 231672¿

Becton Dickinson & Co.

FDA Devices Moderate Feb 14, 2024

AbsorbaTack Absorbable Fixation Device 30 Violet Absorbable Tacks 5 mm- -intended for fixation of prosthetic material to soft tissue in minimally in…

Covidien LP

FDA Devices Moderate Feb 14, 2024

Flow-i C30 Anesthesia System, model 6677300

Getinge Usa Sales Inc

FDA Devices Moderate Feb 14, 2024

Article No. NA6050411, Valiant PhD No. 1 Econo

Ivoclar Vivadent, Inc.

FDA Devices Moderate Feb 14, 2024

BD BBL Sensi Disc Cefixime - 5 ug¿, used for semi-quantitative in vitro susceptibility testing. Catalog Number 231664¿

Becton Dickinson & Co.

FDA Devices Critical Feb 14, 2024

Cardinal Health Monoject, 6 mL Syringe Luer-Lock Tip Soft Pack, REF 1180600777

Cardinal Health 200, LLC

FDA Devices Moderate Feb 14, 2024

DxI 9000 Access Immunoassay Analyzer running software version 1.16 or prior,

Beckman Coulter, Inc.

FDA Devices Moderate Feb 14, 2024

Dual Articulating Headrest, Pad Ret P/N P141210805, REF BF754

Steris Corporation

NHTSA Critical Feb 14, 2024

AUDI 2015-2020: FUEL SYSTEM, GASOLINE

AUDI

NHTSA Critical Feb 13, 2024

GENESIS,HYUNDAI 2015-2019: ELECTRICAL SYSTEM:STARTER ASSEMBLY:SOLENOID

GENESIS,HYUNDAI

NHTSA Critical Feb 13, 2024

HYUNDAI 2024: ENGINE AND ENGINE COOLING:ENGINE:HARD PARTS INTERNAL/MECHANICAL

HYUNDAI

NHTSA Critical Feb 12, 2024

BMW,MINI 2023-2025: ELECTRONIC STABILITY CONTROL (ESC)

BMW,MINI

NHTSA Critical Feb 9, 2024

FORD 2023-2024: POWER TRAIN:DRIVELINE:DRIVESHAFT

FORD

NHTSA Critical Feb 9, 2024

MERCEDES-BENZ 2021-2023: ELECTRICAL SYSTEM:WIRING

MERCEDES-BENZ

NHTSA Critical Feb 9, 2024

FORD,LINCOLN 2018-2020: SEAT BELTS:PRETENSIONER

FORD,LINCOLN

NHTSA Critical Feb 9, 2024

FORD 2021-2022: STEERING:HYDRAULIC POWER ASSIST:HOSE, PIPING, AND CONNECTIONS

FORD

CPSC Moderate Feb 8, 2024

Children's Bathrobes Recalled Due to Burn Hazard and Violation of Flammability Regulations; Sold by Nanchang Zhongcangjishi E-commerce

Nanchang Zhongcangjishi E-commerce Co. Ltd, of China

CPSC Moderate Feb 8, 2024

Electrolux Group Recalls Frigidaire Side by Side Refrigerators with Slim Ice Buckets Due to Choking and Laceration Hazards

CPSC Moderate Feb 8, 2024

GPU Angled Adapters Recalled Due to Fire and Burn Hazards; Manufactured by CableMod

CableMod Ltd., of China

CPSC Moderate Feb 8, 2024

Husqvarna Recalls Grass Trimmers Due to Fire Hazard

Husqvarna Professional Products Inc., of Charlotte, N.C.

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 + USDA FSIS — consumer product, vehicle, and meat/poultry recall feeds for 2024