PlainRecalls

2024 Recalls

6,210 recalls · Page 86 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 8 critical, 42 moderate, and 0 lower-severity recalls. The page references 14 distinct recalling firms operating in 1 distinct product categories, with 50 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 Apr 24, 2024

Intera 1.5T Omni/Stellar, Magnetic Resonance System.

Philips North America Llc

FDA Devices Moderate Apr 24, 2024

Achieva 3.0T, Magnetic Resonance System.

Philips North America Llc

FDA Devices Moderate Apr 24, 2024

Masimo Rad-G, Pulse Oximeter (W/Sensor), REF:9847, Rx Only,

Masimo Corporation

FDA Devices Moderate Apr 24, 2024

Actim PROM dipstik, REF 30831ETUS; qualitative immunoassay rapid test for rupture of fetal membrane

ACTIM OY

FDA Devices Critical Apr 24, 2024

AW-M0001 SONARMED MONITOR. Used in conjunction with SonarMed Acoustic Sensors for airway monitoring.

SonarMed Inc

FDA Devices Moderate Apr 24, 2024

GYROSCAN T5-NT, Magnetic Resonance System.

Philips North America Llc

FDA Devices Moderate Apr 24, 2024

Intera 1.5T, Magnetic Resonance System.

Philips North America Llc

FDA Devices Critical Apr 24, 2024

AW-S035 NEO SONARMED SENSOR 3.5MM. Used in conjunction with SonarMed Monitor for airway monitoring.

SonarMed Inc

FDA Devices Moderate Apr 24, 2024

Intera 1.5T Achieva Nova, Magnetic Resonance System.

Philips North America Llc

FDA Devices Critical Apr 24, 2024

AW-S025 NEO SONARMED SENSOR 2.5MM. Used in conjunction with SonarMed Monitor for airway monitoring.

SonarMed Inc

FDA Devices Critical Apr 24, 2024

Tablo Hemodialysis System, REF: PN-0003000, PN-0006000 and PN-0007001

Outset Medical, Inc.

FDA Devices Moderate Apr 24, 2024

Intera 1.5T Achieva IT Nova, Magnetic Resonance System.

Philips North America Llc

FDA Devices Moderate Apr 24, 2024

Intera 1.0T Omni/Stellar, Magnetic Resonance System.

Philips North America Llc

FDA Devices Moderate Apr 24, 2024

GYROSCAN ACS-NT, Magnetic Resonance System.

Philips North America Llc

FDA Devices Moderate Apr 24, 2024

Smiths Medical Medfusion Model 4000 Syringe pump, Item Numbers: a) 4000-0101-249, b) 4000-0101-50, c) 4000-0101-51, d) 4000-0105-249, e) 4…

Smiths Medical ASD Inc.

FDA Devices Moderate Apr 24, 2024

Achieva XR, Magnetic Resonance System.

Philips North America Llc

FDA Devices Moderate Apr 24, 2024

Intera 1.5T Achieva Nova-Dual, Magnetic Resonance System.

Philips North America Llc

FDA Devices Moderate Apr 24, 2024

Ingenia 1.5T CX, Magnetic Resonance System.

Philips North America Llc

FDA Devices Moderate Apr 24, 2024

Surgical Tools and Cardiovascular Specialty marketing brochures, Reference numbers: US-AS18-210002 Surgical Tools Brochure 2021, US-AS18-210004 Surg…

Baxter Healthcare Corporation

FDA Devices Moderate Apr 24, 2024

Smiths Medical Medfusion Guide Barrel Clamp, Item number G6000716

Smiths Medical ASD Inc.

FDA Devices Moderate Apr 24, 2024

Surgical Tools and Cardiovascular Specialty marketing brochures, Reference numbers: US-AS18-210002 Surgical Tools Brochure 2021, US-AS18-210004 Surg…

Baxter Healthcare Corporation

FDA Devices Moderate Apr 24, 2024

Ingenia Elition S, Magnetic Resonance System.

Philips North America Llc

FDA Devices Moderate Apr 24, 2024

Atellica CH Iron3 - IVD use in the quantitative measurement of iron in human serum and plasma (lithium heparin and sodium heparin) using the Atellica…

Siemens Healthcare Diagnostics, Inc.

FDA Devices Moderate Apr 24, 2024

Microalbumin Calibrator Series (mALB CAL)-IVD used to calibrate the Microalbumin Assay Catalog Number: MA1567

Randox Laboratories Ltd.

FDA Devices Moderate Apr 24, 2024

Masimo Rad-G, Pulse Oximeter (W/Patient Cable), REF:9895 Rx Only,

Masimo Corporation

FDA Devices Moderate Apr 24, 2024

Microalbumin Calibrator Series (mALB CAL)-IVD to calibrate the Microalbumin Assay Catalog Number: MA2426

Randox Laboratories Ltd.

FDA Devices Moderate Apr 24, 2024

Peel-Away Introducer - Intended for the percutaneous introduction of balloon, electrode and closed or non-tapered end catheters into central and peri…

Cook Incorporated

FDA Devices Moderate Apr 24, 2024

Intera 1.5T Explorer/Nova Dual, Magnetic Resonance System.

Philips North America Llc

FDA Devices Moderate Apr 24, 2024

POLYSIN (Polyglycolic Acid) suture, HSM9 5-0 BR PGA Part Number G503N

SURGICAL SPECIALTIES

FDA Devices Critical Apr 24, 2024

AW-S030 NEO SONARMED SENSOR 3.0MM. Used in conjunction with SonarMed Monitor for airway monitoring.

SonarMed Inc

FDA Devices Moderate Apr 24, 2024

Surgical Tools and Cardiovascular Specialty marketing brochures, Reference numbers: US-AS18-210002 Surgical Tools Brochure 2021, US-AS18-210004 Surg…

Baxter Healthcare Corporation

FDA Devices Moderate Apr 24, 2024

Dilator - Intended to be used for dilating puncture sites or catheter tracts for percutaneous placement of devices for vascular and non-vascular appl…

Cook Incorporated

FDA Devices Critical Apr 24, 2024

LifeVentEVO2, all software versions except 1.05.06.00. Ventilator for pediatric and adult patients. (sold outside US)

Philips Respironics, Inc.

FDA Devices Critical Apr 24, 2024

Aeris EVO, all software versions except 1.05.06.00. Ventilator for pediatric and adult patients. (sold outside US)

Philips Respironics, Inc.

FDA Devices Moderate Apr 24, 2024

Identity Imprint PS Tibial Tray Size 4: Lot 540287

Conformis, Inc.

FDA Devices Moderate Apr 24, 2024

Entuit Secure Adjustable Gastrointestinal Suture Anchor Set - Intended for anchoring the anterior wall of the stomach to the abdominal wall prior to …

Cook Incorporated

FDA Devices Moderate Apr 24, 2024

Masimo Rad-G, Pulse Oximeter with temperature (W/Sensor), REF:9210, Rx Only,

Masimo Corporation

FDA Devices Moderate Apr 24, 2024

Ingenia Elition X, Magnetic Resonance System.

Philips North America Llc

FDA Devices Moderate Apr 24, 2024

Enterprise 1.5T, Magnetic Resonance System.

Philips North America Llc

FDA Devices Moderate Apr 24, 2024

Yueh Centesis Disposable Catheter Needle - Intended for use in percutaneous fluid aspirations, such as paracentesis or thoracentesis. REFERENCE P…

Cook Incorporated

FDA Devices Moderate Apr 24, 2024

Trocar Needle - Used for dilating puncture sites or catheter tracts for percutaneous placement of devices for vascular and non-vascular applications …

Cook Incorporated

FDA Devices Moderate Apr 24, 2024

MR 7700, Magnetic Resonance System.

Philips North America Llc

FDA Devices Moderate Apr 24, 2024

GYROSCAN T5, Magnetic Resonance System.

Philips North America Llc

FDA Devices Moderate Apr 24, 2024

Intera Achieva 1.5T Pulsar, Magnetic Resonance System.

Philips North America Llc

FDA Devices Moderate Apr 24, 2024

Achieva 3.0TX for PET, Magnetic Resonance System.

Philips North America Llc

FDA Devices Moderate Apr 24, 2024

Smiths Medical Medfusion Model 3500 Syringe pumps, Item Numbers: a) 3500 b) 3500-0600-00 c) 3500-0600-01 d) 3500-0600-249 e) 3500-0600-50 f) …

Smiths Medical ASD Inc.

FDA Devices Moderate Apr 24, 2024

Intera CV, Magnetic Resonance System.

Philips North America Llc

FDA Devices Critical Apr 24, 2024

Trilogy Evo O2, all software versions except 1.05.06.00. Ventilator for pediatric and adult patients.

Philips Respironics, Inc.

FDA Devices Moderate Apr 24, 2024

Masimo Rad-G, Pulse Oximeter (W/Patient Cable), REF:9849, Rx Only,

Masimo Corporation

FDA Devices Moderate Apr 24, 2024

Siemens Artis Models: Interventional Fluoroscopic X-Ray Systems-Models: Artis zee floor- 10094135 Artis zee ceiling- 10094137 Artis zee multi-purp…

Siemens Medical Solutions USA, Inc

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.