PlainRecalls

2024 Recalls

Compiled from official public sources by the editorial team.

6,210 recalls · Page 30 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 3 critical, 47 moderate, and 0 lower-severity recalls. The page references 20 distinct recalling firms operating in 2 distinct product categories, with 49 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Devices (49), NHTSA (1), 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 Oct 2, 2024

AVS Anchor-C Cervical Cage System Instructions For Use (IFU)- eIFU (revision 5)-Indicated for anterior cervical interbody fusion procedures in skelet…

Stryker Spine

FDA Devices Moderate Oct 2, 2024

AGILE ESO FC RMV 23MM X 15.0CM IN 18.5 F- Agile Esophageal Partially Covered (PC) and Fully Covered (FC) OTW Stent System is intended for maintaini…

Boston Scientific Corporation

FDA Devices Moderate Oct 2, 2024

Stryker TMJ Unilateral Implant, REF: GHG010, consisting of the following components: Ref: CHG010AM, Anatomical Bone Model, Accessory, REF: CHG010RF,…

TMJ Solutions Inc

FDA Devices Moderate Oct 2, 2024

Ingenia 1.5T -For use as a diagnostic device to obtain cross-sectional images, spectroscopic images and/or spectra of the internal structure of the h…

Philips North America Llc

FDA Devices Moderate Oct 2, 2024

SmartPath to Ingenia Elition X - For use as a diagnostic device to obtain cross-sectional images, spectroscopic images and/or spectra of the internal…

Philips North America Llc

FDA Devices Moderate Oct 2, 2024

WALLFLEX FC ESO STENT RMV LL 23X125-Wallflex Esophageal Partially Covered (PC) and Fully Covered (FC) Stent System Intended for maintaining esophagea…

Boston Scientific Corporation

FDA Devices Moderate Oct 2, 2024

Cysto, FTCY03L; Medical convenience kit

American Contract Systems, Inc.

FDA Devices Moderate Oct 2, 2024

Biodesign Fistula Plug C-FPS-0.2 - For implantation to reinforce soft tissue for repair of recto-vaginal or anorectal fistulas. Order Number (GPN)…

Cook Biotech, Inc.

FDA Devices Moderate Oct 2, 2024

Karl Storz - Endoskope , REF: 27295AA, Hopkins Telescope 6, 18 Fr, Rx only, CE 0123

Karl Storz Endoscopy

FDA Devices Moderate Oct 2, 2024

Biodesign Fistula Plug C-FPS-0.4-2 - For implantation to reinforce soft tissue for repair of recto-vaginal or anorectal fistulas. Order Number (GPN)…

Cook Biotech, Inc.

FDA Devices Moderate Oct 2, 2024

The device is a mobile x-ray system designed to work with Fujifilm's GOS and CsI scintillator FDR D-EVO2 (DR-ID) 12XXSE) family of digital x-ray dete…

FUJIFILM Healthcare Americas Corporation

FDA Devices Moderate Oct 2, 2024

Biodesign Fistula Plug C-FPB-0.4 - For implantation to reinforce soft tissue for repair of recto-vaginal or anorectal fistulas. Order Number (GPN): …

Cook Biotech, Inc.

FDA Devices Moderate Oct 2, 2024

WALLFLEX FC ESO STENT RMV LL 23X105- Intended for maintaining esophageal luminal patency in esophageal strictures caused by intrinsic and/or extrinsi…

Boston Scientific Corporation

FDA Devices Moderate Oct 2, 2024

Origio Sperm Wash Medium Pack of Ten 10ml bottles - Intended for washing of spermatozoa Part Number: 84051010A

CooperSurgical, Inc.

FDA Devices Moderate Oct 2, 2024

Ingenia Elition S -For use as a diagnostic device to obtain cross-sectional images, spectroscopic images and/or spectra of the internal structure of …

Philips North America Llc

FDA Devices Moderate Oct 2, 2024

Essentia MAJ Laparotomy Std Pack, ESLT53B; Medical convenience kit

American Contract Systems, Inc.

FDA Devices Moderate Oct 2, 2024

AGILE ESO OTW FC 23MM X 10.1CM IN 18.5 F-Agile Esophageal Partially Covered (PC) and Fully Covered (FC) OTW Stent System is intended for maintaining…

Boston Scientific Corporation

FDA Devices Moderate Oct 2, 2024

Day Surgery General Pack, FHGE18T; Medical convenience kit

American Contract Systems, Inc.

FDA Devices Moderate Oct 2, 2024

BioPince Ultra Full Core Biopsy Instrument: REF: REF: 360-1080-01, 360-1080-02, 360-1080-03, 360-1580-01, 360-1580-02, 360-1580-03, 360-2080-01, 360-…

Argon Medical Devices, Inc

FDA Devices Moderate Oct 2, 2024

Karl Storz - Endoskope , REF: 27293AA, Hopkins Telescope 6, Rx only, CE 0123

Karl Storz Endoscopy

FDA Devices Moderate Oct 2, 2024

Endovascular AAA Pack, ESED52B; Medical convenience kit

American Contract Systems, Inc.

FDA Devices Moderate Oct 2, 2024

MR 5300 - For use as a diagnostic device to obtain cross-sectional images, spectroscopic images and/or spectra of the internal structure of the head,…

Philips North America Llc

FDA Devices Moderate Oct 2, 2024

Biodesign Fistula Plug C-FPS-0.2-2 - For implantation to reinforce soft tissue for repair of recto-vaginal or anorectal fistulas. Order Number (GP…

Cook Biotech, Inc.

FDA Devices Moderate Oct 2, 2024

Creatine Kinase (CK) used on cobas c 311/501/502 and COBAS INTEGRA 400 plus-In vitro test for the quantitative determination of creatine kinase (CK) …

Roche Diagnostics Operations, Inc.

FDA Devices Moderate Oct 2, 2024

IntelliVue Patient Monitor MX400 (Model Number 866060), MX430 (Model Number 866061), MX450 (Model Number 866062), MX500 (Model Number 866064), and MX…

Philips North America

FDA Devices Moderate Oct 2, 2024

Karl Storz - Endoskope , REF: 27840KA, Nephroscope for MIP L, Rx only, CE 0123

Karl Storz Endoscopy

FDA Devices Moderate Oct 2, 2024

Prelude Sheath Introducer 7.5F, REF: PSI-7F-11-038 Version F (PSI-7F-11-038/F)

Merit Medical Systems, Inc.

FDA Devices Critical Oct 2, 2024

CARDIOSAVE HYBRID INTRA-AORTIC BALLOON PUMP (IABP). Electromechanical system used to inflate and deflate intra-aortic balloons.

Datascope Corp.

FDA Devices Moderate Oct 2, 2024

Biodesign Recto-Vaginal Fistula Plug RVP-0.4 - For implantation to reinforce soft tissue for repair of recto-vaginal fistulas. Order Number (GPN):…

Cook Biotech, Inc.

FDA Devices Moderate Oct 2, 2024

BARD MAGNUM Disposable Core Tissue Biopsy Needle REF: MN1410 MN 1420 MN1610 MN1616 MN1820 MN2010 The Magnum Biopsy System (instrument and ne…

Bard Peripheral Vascular Inc

FDA Devices Moderate Oct 2, 2024

ENT, COEN27N; Medical convenience kit

American Contract Systems, Inc.

FDA Devices Moderate Oct 2, 2024

AGILE ESO OTW FC 23MM X 15.0CM IN 18.5 F-Agile Esophageal Partially Covered (PC) and Fully Covered (FC) OTW Stent System is intended for maintaining…

Boston Scientific Corporation

FDA Devices Moderate Oct 2, 2024

MR 7700 -For use as a diagnostic device to obtain cross-sectional images, spectroscopic images and/or spectra of the internal structure of the head,…

Philips North America Llc

FDA Devices Moderate Oct 2, 2024

Biodesign Fistula Plug C-FPS-0.7 - For implantation to reinforce soft tissue for repair of recto-vaginal or anorectal fistulas. Order Number (GPN)…

Cook Biotech, Inc.

FDA Devices Moderate Oct 2, 2024

AGILE ESO OTW PC 23MM X 12.0CM IN 18.5 F-Agile Esophageal Partially Covered (PC) and Fully Covered (FC) OTW Stent System is intended for maintaining…

Boston Scientific Corporation

FDA Devices Critical Oct 2, 2024

paraPAC 300 ventilator kit without internal PEEP and CPAP, Item Number P300N

Smiths Medical ASD Inc.

FDA Devices Moderate Oct 2, 2024

Origio Sperm Wash Medium Pack of Five 60ml bottles - Intended for washing of spermatozoa. Part Number: 84055060A

CooperSurgical, Inc.

FDA Devices Moderate Oct 2, 2024

WALLFLEX FC ESO STENT RMV 23X125MM- Wallflex Esophageal Partially Covered (PC) and Fully Covered (FC) Stent System Intended for maintaining esophagea…

Boston Scientific Corporation

FDA Devices Moderate Oct 2, 2024

Silver-Plated Copper Sims Uterine Sound, Part Number 64-600

CooperSurgical, Inc.

FDA Devices Moderate Oct 2, 2024

(a) CardinalHealth Salem Sump Dual Lumen Stomach Tube, 12 Fr/Ch (4.0 mm) x 48 in. (122 cm), Model #8888264929, Sterile; (b) CardinalHealth Salem …

Cardinal Health 200, LLC

FDA Devices Moderate Oct 2, 2024

Arthroscopy Pack, MSKA45A; Medical convenience kit

American Contract Systems, Inc.

FDA Devices Moderate Oct 2, 2024

GE Giraffe Warmer, Model/Catalog Number M1118179-01090979. Infant radiant warmers provide infrared heat in a controlled manner to neonates who are un…

Wipro GE Healthcare Private Ltd.

FDA Devices Moderate Oct 2, 2024

Karl Storz - Endoskope , REF: 27830KA, Nephroscope for MIP M, Rx only, CE 0123

Karl Storz Endoscopy

FDA Devices Moderate Oct 2, 2024

AGILE ESO OTW PC 23MM X 10.1CM IN 18.5 F-Agile Esophageal Partially Covered (PC) and Fully Covered (FC) OTW Stent System is intended for maintaining…

Boston Scientific Corporation

FDA Devices Moderate Oct 2, 2024

Biodesign Fistula Plug C-FPS-0.4 - For implantation to reinforce soft tissue for repair of recto-vaginal or anorectal fistulas. Order Number (GPN): …

Cook Biotech, Inc.

FDA Devices Moderate Oct 2, 2024

Selenia Dimensions/ 3Dimensions-Digital breast tomosynthesis Software Version Dimensions 1.12.0 and 3Dimensions 2.3.0 system software as follows Mo…

Hologic Inc

FDA Devices Moderate Oct 2, 2024

Open Shoulder, LWOS39L; Medical convenience kit

American Contract Systems, Inc.

FDA Devices Moderate Oct 2, 2024

WALLFLEX PC ESOPH STENT 18/23MM X 103MM- Wallflex Esophageal Partially Covered and Fully Covered Stent System is Intended for maintaining esophageal …

Boston Scientific Corporation

FDA Devices Moderate Oct 2, 2024

AGILE ESO FC RMV 23MM X 10.1CM IN 18.5 F-Agile Esophageal Partially Covered (PC) and Fully Covered (FC) OTW Stent System is intended for maintaining…

Boston Scientific Corporation

NHTSA Critical Oct 2, 2024

BMW 2023-2024: ELECTRONIC STABILITY CONTROL (ESC)

BMW

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 July 2026.