PlainRecalls

2024 Recalls

6,210 recalls · Page 110 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 11 critical, 39 moderate, and 0 lower-severity recalls. The page references 19 distinct recalling firms operating in 1 distinct product categories, with 41 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Devices (50), 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 Feb 14, 2024

RX Series Copper (Cu) Assay Ref. Number CU2340

Randox Laboratories Ltd.

FDA Devices Moderate Feb 14, 2024

Spectral CT 7500: Software Version 5.0, Model 728333 and Spectral CT 7500 China: Software Version 5.0, Model 728340.

PHILIPS MEDICAL SYSTEMS

FDA Devices Moderate Feb 14, 2024

BD BBL Sensi Disc Cefotaxime - 30 ug¿, used for semi-quantitative in vitro susceptibility testing. Catalog Number 231606 and 231607¿; 5 ug, Catalog …

Becton Dickinson & Co.

FDA Devices Critical Feb 14, 2024

Cardinal Health Monoject, 20 mL Syringe Luer-Lock Tip Soft Pack, REF 1182000777

Cardinal Health 200, LLC

FDA Devices Critical Feb 14, 2024

Cardinal Health Monoject, 12 mL Syringe Luer-Lock Tip Soft Pack, REF 1181200777T

Cardinal Health 200, LLC

FDA Devices Moderate Feb 14, 2024

BD BBL Sensi Disc Tetracycline 30 ug,used for semi-quantitative in vitro susceptibility testing. Catalog Number 230998 and 231344¿

Becton Dickinson & Co.

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

FDA Devices Moderate Feb 14, 2024

Brasseler 8S RA SHP RD (Super-Sharp Round) H1S.21.023, REF 001156T0), carbide dental bur, 10 burs/package, Rx.

Brasseler USA I Lp

FDA Devices Moderate Feb 14, 2024

BO-RF-32-USA RotaFlow Centrifugal Pump with SOFTLINE Coating, Product Code 701047553. For use with an extracorporeal cardiovascular or cardiopulmonar…

Maquet Medical Systems USA

FDA Devices Moderate Feb 14, 2024

FilmArray Pneumonia Panel (Pneumo), REF: FIT-ASY-0144, CED 2797, IVD, Rx Only (30 test kit)

BioFire Diagnostics, LLC

FDA Devices Moderate Feb 14, 2024

BD BBL Sensi Disc Ampicillin - 10 ¿g, Catalog No. 230705 and 231264; 2 ¿g, Catalog No. 231263. Used for semi-quantitative in vitro susceptibility tes…

Becton Dickinson & Co.

FDA Devices Moderate Feb 14, 2024

Guardian 4 Glucose Sensor, REF: MMT-7040A, MMT-7040C1, MMT-7040C2, MMT-7040C3, MMT-7040D1, MMT-7040D2, MMT-7040MA, MMT-7040QC1, MMT-7040QC2, MMT-7040…

Medtronic MiniMed, Inc.

FDA Devices Critical Feb 14, 2024

Cardinal Health Monoject, 60mL Enteral Syringe (purple) - For Use with ENFit Connection System, REF 460SE

Cardinal Health 200, 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.