PlainRecalls

2024 Recalls

6,210 recalls · Page 51 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 6 critical, 43 moderate, and 1 lower-severity recalls. The page references 20 distinct recalling firms operating in 2 distinct product categories, with 45 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Devices (47), NHTSA (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 Aug 14, 2024

Luminos Agile Max -Intended to visualize anatomical structures by converting an x-ray pattern into a visible image. Model Number: 10762472

Siemens Medical Solutions USA, Inc

FDA Devices Moderate Aug 14, 2024

3.0T SIGNA HDxt Family, with affected software versions: RX27.0 to RX27.3, RX28.0, RX29.0 to RX29.2, MR30.0, MR30.1HD16.0_V03, HD23.0_V03; Nuclear M…

GE Medical Systems, LLC

FDA Devices Moderate Aug 14, 2024

American Contract Systems Hand Pack convenience kit

American Contract Systems, Inc.

FDA Devices Moderate Aug 14, 2024

BIOFIRE FILMARRAY Gastrointestinal (GI) Panel REF RFIT-ASY-0116 (30 test kit) BIOFIRE FILMARRAY Gastrointestinal (GI) Panel REF RFIT-ASY-0104 (6…

BioFire Diagnostics, LLC

FDA Devices Moderate Aug 14, 2024

American Contract Systems Biopsy Drape Pack convenience kit

American Contract Systems, Inc.

FDA Devices Moderate Aug 14, 2024

Baxter PST 500 U, Precision Surgical Table, Part number (product code) 4080300

Baxter Healthcare Corporation

FDA Devices Moderate Aug 14, 2024

Verigene Gram Positive Blood Culture (BC-GP) Nucleic Acid Test

Luminex Corporation

FDA Devices Moderate Aug 14, 2024

SIGNA Victor, with affected software versions: MR30.1; Nuclear Magnetic Resonance Imaging System

GE Medical Systems, LLC

FDA Devices Moderate Aug 14, 2024

TruDi NAV Suction, 0 Degrees; Model/Catalog Number: TDNS000Z. TruDi" NAV Suction Instruments are intended for use with the TruDi" Navigation Syst…

Integra LifeSciences Corp.

FDA Devices Moderate Aug 14, 2024

IntelliVue Patient Monitor MX450 with L.x and M.x; K.x provided with L.x entitlements Model Number: 866062. Indicated for use by health care pro…

Philips North America Llc

FDA Devices Moderate Aug 14, 2024

IntelliVue Patient Monitor MX550 with L.x and M.x; K.x provided with L.x entitlements Model Number: 866066. Indicated for use by health care prof…

Philips North America Llc

FDA Devices Moderate Aug 14, 2024

Discovery MR950, with affected software versions: 7T23.0; Nuclear Magnetic Resonance Imaging System - research use only

GE Medical Systems, LLC

FDA Devices Moderate Aug 14, 2024

SIGNA Artist, with affected software versions: DV26.0, DV27.1, DV28.1, DV29.1, MR30.0, MR30.1; Nuclear Magnetic Resonance Imaging System

GE Medical Systems, LLC

FDA Devices Moderate Aug 14, 2024

SIGNA Hero, with affected software versions: PX29.1, MR30.0, MR30.1; Nuclear Magnetic Resonance Imaging System

GE Medical Systems, LLC

FDA Devices Moderate Aug 14, 2024

SIGNA Premier, with affected software versions: RX27.0 to RX27.3, RX28.0, RX29.0 to RX29.2, MR30.0, MR30.1; Nuclear Magnetic Resonance Imaging System

GE Medical Systems, LLC

FDA Devices Moderate Aug 14, 2024

BD PYXIS MEDBANK TWR MN CR-2HH-6FM, REF: 169-89 containing software version 3.9.1.9

CareFusion 303, Inc.

FDA Devices Moderate Aug 14, 2024

SIGNA MAGNUS, with affected software versions: MR29.1, RX29.1; Nuclear Magnetic Resonance Imaging System - research use only

GE Medical Systems, LLC

FDA Devices Moderate Aug 14, 2024

CryoValve SG Pulmonary Human Heart Valve, SGPV00, Cryopreserved Decellularized Heart Valve Allograft Prepared with SynerGraft (SG) Technology.

Artivion, Inc

FDA Devices Moderate Aug 14, 2024

Hookup Model/Catalog Number: DSD-110-HU0163 Product Description: Hookups provide the interface between DSD Automated Endoscope Reprocessors ( AER…

Steris Corporation

FDA Devices Critical Aug 14, 2024

Puritan Bennett 500 Series Ventilators (Description/REF): PURITAN BENNETT 560 VENTILATOR/4096600, PURITAN BENNETT PB560 VENTILATOR EU-DIV/4096600-0…

Covidien

FDA Devices Moderate Aug 14, 2024

1.5T SIGNA HDxt Family, with affected software versions: HD16.0_V03 to HD16.4, HD23.0_V03, HD28.0, HD29.1, MR30.0, MR30.1; Nuclear Magnetic Resonanc…

GE Medical Systems, LLC

FDA Devices Moderate Aug 14, 2024

BD PYXIS MEDBANK MINI CR-4HH-P, REF: 169-115 containing software version 3.9.1.9

CareFusion 303, Inc.

FDA Devices Moderate Aug 14, 2024

BD PYXIS MEDBANK TWR MN CR-6HH-2FH-2FM-P, REF: 169-93 containing software version 3.9.1.9

CareFusion 303, Inc.

FDA Devices Moderate Aug 14, 2024

Luminos dRF Max- Intended to visualize anatomical structures by converting an x-ray pattern into a visible image. Model Number: 10762471

Siemens Medical Solutions USA, Inc

FDA Devices Moderate Aug 14, 2024

American Contract Systems Laparoscopy Litho Std Pack convenience kit and American Contract Systems Lap Chole convenience kit

American Contract Systems, Inc.

FDA Devices Moderate Aug 14, 2024

SIGNA Prime, with affected software versions: MR30.1; Nuclear Magnetic Resonance Imaging System

GE Medical Systems, LLC

FDA Devices Moderate Aug 14, 2024

American Contract Systems Special Procedure Pack convenience kit

American Contract Systems, Inc.

FDA Devices Moderate Aug 14, 2024

American Contract Systems Cataract Pack convenience kit

American Contract Systems, Inc.

FDA Devices Moderate Aug 14, 2024

SIGNA Pioneer, with affected software versions: PX25.0 to PX25.5, PX26.0, PX26.1, PX28.0 to PX28.4, PX29.0, PX29.1, MR30.0, MR30.1; Nuclear Magnetic…

GE Medical Systems, LLC

FDA Devices Moderate Aug 14, 2024

American Contract Systems Extremity convenience kit, American Contract Systems Hand Pack convenience kit, and American Contract Systems Total Knee Pa…

American Contract Systems, Inc.

FDA Devices Moderate Aug 14, 2024

BD PYXIS MEDBANK TWR MN CR-6HH-4FM-P, REF: 169-94 containing software version 3.9.1.9

CareFusion 303, Inc.

FDA Devices Moderate Aug 14, 2024

The Everest Bipolar Cutting Forceps are intended to be passed through a 5-mm or 10-mm cannula, depending on the model/outer diameter size of the forc…

Olympus Corporation of the Americas

FDA Devices Critical Aug 14, 2024

Medline procedure kits labeled as: 1) CONTINUOUS BLOCK, Pack Number DYNJRA0960C; 2) COMBINED SPINAL AND EPIDURAL, Pack Number DYNJRA1268C; 3) …

MEDLINE INDUSTRIES, LP - Northfield

FDA Devices Moderate Aug 14, 2024

BD PYXIS MEDBANK TWR MN CR-10HH-2FH-P, REF: 169-82 containing software version 3.9.1.9

CareFusion 303, Inc.

FDA Devices Critical Aug 14, 2024

CADD-Solis Ambulatory Infusion Pumps, Model 2100. Intended for the following uses: Indicated for the following uses: Intra-arterial, subcutaneous, …

Smiths Medical ASD Inc.

FDA Devices Moderate Aug 14, 2024

Multitom Rax -Intended to visualize anatomical structures by converting an x-ray pattern into a visible image Model Number: 10860700

Siemens Medical Solutions USA, Inc

FDA Devices Moderate Aug 14, 2024

BD PYXIS MEDBANK TWR MN CR-14HH-P, REF: 169-86 containing software version 3.9.1.9

CareFusion 303, Inc.

FDA Devices Low Aug 14, 2024

NavaClick Syringe and Needle, Model Number LIN02

LINEAGE BIOMEDICAL, INC

FDA Devices Moderate Aug 14, 2024

BD PYXIS MEDBANK TWR MN CR-8HH-2FH-1FM-P, REF: 169-97 containing software version 3.9.1.9

CareFusion 303, Inc.

FDA Devices Moderate Aug 14, 2024

Leica HistoCore Arcadia H, REF: 14039354100 and 14039357258, Paraffin Embedding Station.

LEICA BIOSYSTEMS NUSSLOCH GMBH

FDA Devices Moderate Aug 14, 2024

Soltive SuperPulsed Laser System Wireless Footswitch, Model TFL-AFSWL

Olympus Corporation of the Americas

FDA Devices Moderate Aug 14, 2024

Discovery MR750w 3.0T, with affected software versions: DV24.0, DV25.0, DV25.1, DV26.0 to DV26.5, DV29.1, MR30.0, MR30.1; Nuclear Magnetic Resonance…

GE Medical Systems, LLC

FDA Devices Moderate Aug 14, 2024

BD PYXIS MEDBANK TWR MN CR-8HH-3FM-P, REF: 169-99 containing software version 3.9.1.9

CareFusion 303, Inc.

FDA Devices Moderate Aug 14, 2024

American Contract Systems Gyn Laparoscopy convenience kit

American Contract Systems, Inc.

FDA Devices Critical Aug 14, 2024

CADD-Solis VIP ambulatory Infusion Pumps, Model 2110. Indicated for the following uses: Intra-arterial, subcutaneous, intraperitoneal, in close pro…

Smiths Medical ASD Inc.

FDA Devices Moderate Aug 14, 2024

Brivo MR355, with affected software versions: SV20.3, SV23.3, MR30.0, MR30.1; Nuclear Magnetic Resonance Imaging System

GE Medical Systems, LLC

FDA Devices Moderate Aug 14, 2024

Soltive Pro SuperPulsed Laser System, Model TFL-SLS

Olympus Corporation of the Americas

NHTSA Critical Aug 13, 2024

BMW 2012-2018: ENGINE AND ENGINE COOLING:COOLING SYSTEM:PUMP

BMW

NHTSA Critical Aug 10, 2024

FORD 2020-2022: ENGINE

FORD

NHTSA Moderate Aug 9, 2024

FORD,LINCOLN 2024: VISIBILITY:POWER WINDOW DEVICES AND CONTROLS

FORD,LINCOLN

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.