PlainRecalls

2024 Recalls

6,210 recalls · Page 122 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 2 critical, 48 moderate, and 0 lower-severity recalls. The page references 26 distinct recalling firms operating in 6 distinct product categories, with 40 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Devices (41), CPSC (4), FDA Food (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, or NHTSA for the system-of-record on any specific recall. PlainRecalls indexes this archive for research and consumer awareness purposes.

FDA Devices Moderate Jan 17, 2024

Detector H. Pylori, Catalog Number IHP-30

Immunostics, Inc.

FDA Devices Moderate Jan 17, 2024

CD11b APC: ASR, REF: 340936, and CE, REF: 333143

Becton, Dickinson and Company, BD Biosciences

FDA Devices Moderate Jan 17, 2024

BrightView, Gamma Camera System, Product Code 882480.

Philips North America

FDA Devices Moderate Jan 17, 2024

Model No. CYF-V2R, VISERA Cysto-Nephro Videoscope

Shirakawa Olympus Co., Ltd.

FDA Devices Moderate Jan 17, 2024

Abiomed Oscor Introducer Kit, 14Fr x Long Individual (0052-0017)- Introducer(s) are intended for introduction of the Impella Catheter into the body. …

Abiomed, Inc.

FDA Devices Moderate Jan 17, 2024

ARCHITECT c4000 Processing Module REF: 02P24-01 02P24-02 02P24-40 01R24-56 01R25-56 The Abbott ARCHITECT c4000 Processing Module is designed…

Abbott Laboratories

FDA Devices Moderate Jan 17, 2024

Medline Gown Poly W/Breath Sleeves XL AAMIK Level 4 (Eclipse gown), REF SPT-2208CS, 100/pack, Non-Sterile.

MEDLINE INDUSTRIES, LP - Northfield

FDA Devices Moderate Jan 17, 2024

Model No. CYF-5R, Cystonephrofiberscope

Shirakawa Olympus Co., Ltd.

FDA Devices Moderate Jan 17, 2024

BrightView XCT, Gamma Camera, Product Code 882482

Philips North America

FDA Devices Moderate Jan 17, 2024

Incisive CT, model 728143 & 728144 running Software Version 5.0.0.

Philips Healthcare (Suzhou) Co., Ltd.

FDA Devices Moderate Jan 17, 2024

Abiomed Kit, 14Fr Introducer, 13cm, Long Taper Individual (0052-0038)-Introducer(s) are intended for introduction of the Impella Catheter into the bo…

Abiomed, Inc.

FDA Devices Moderate Jan 17, 2024

Ambu aView 2 A Monitor, Catalog numbers 405011000 and 405011000US2

Ambu Inc.

FDA Devices Moderate Jan 17, 2024

Boston Scientific Model 3120 ZOOM LATITUDE Programmer/Recorder/Monitor (PRM) installed with Model 2892 Programmer Application Software used for the f…

Boston Scientific Corporation

FDA Devices Moderate Jan 17, 2024

NIM TriVantage EMG Endotracheal Tubes, Model (REF) Numbers and sizes: a) 8229706, 6.0MM ID; b) 8229707, 7.0MM ID; c) 8229708, 8.0MM ID; d) 822…

Medtronic Xomed, Inc.

FDA Devices Moderate Jan 17, 2024

OLYMPUS ENDOEYE FLEX DEFLECTABLE VIDEOSCOPE (10 mm diameter) Model: LTF-S190-10 Used with a video system center, light source, documentation equi…

Olympus Corporation of the Americas

FDA Devices Moderate Jan 17, 2024

Model No. BF-P190, EVIS EXERA III Bronchovideoscope

Shirakawa Olympus Co., Ltd.

FDA Devices Moderate Jan 17, 2024

BD Recanalization System, REF: BDRECANSYSTEM

Bard Peripheral Vascular Inc

FDA Devices Moderate Jan 17, 2024

Oscor Introducer Kit, 14Fr x Short Individual (0052-0001)- Introducer(s) are intended for introduction of the Impella Catheter into the body. Part N…

Abiomed, Inc.

FDA Devices Moderate Jan 17, 2024

Baxter Coseal Premix, Surgical Sealant, Product Codes: a) 934070; b) 934071; c) 934072

Baxter Healthcare Corporation

FDA Devices Moderate Jan 17, 2024

Vascu-Guard Peripheral Vascular Patch (GLOBAL), Product Codes: a) VG0108N: 0.8X8 CM GLOBAL, b) VG0110N: 1X10 CM GLOBAL, c) VG0106N: 1X6 CM…

Baxter Healthcare Corporation

FDA Devices Moderate Jan 17, 2024

VADER pedicle system, torque wrench, Catalog Number 42-703

Icotec Ag

FDA Devices Moderate Jan 17, 2024

Model No. CYF-5, Cystonephrofiberscope

Shirakawa Olympus Co., Ltd.

FDA Devices Moderate Jan 17, 2024

CUSTOM SPRYSTEP, custom made device dynamic ankle-foot orthosis (AFO) , Ref #s: 17C1000, 17C2000, 17C1010, 17C2010, 17C1040, 17C2040

Townsend Design

FDA Devices Moderate Jan 17, 2024

Baxter Preveleak Surgical Sealant, Product Codes: ADS201808

Baxter Healthcare Corporation

FDA Devices Moderate Jan 17, 2024

Abiomed Kit, 23Fr Introducer, 11cm, Sterile Part of Pump Set (1000323)-Introducer(s) are intended for introduction of the Impella Catheter into the b…

Abiomed, Inc.

FDA Devices Moderate Jan 17, 2024

Olympus ENDOEYE HD II Rigid Videoscope Catalog Numbers: WA50040A, WA50042A -used with a video system center, light source, documentation equipment,…

Olympus Corporation of the Americas

FDA Devices Moderate Jan 17, 2024

Baxter Ostene Hemostasis Material, Product Codes: a) 1503831, 3.5 G; b) 1503832, 2.5 G; c) 1503833, 1.0 G

Baxter Healthcare Corporation

FDA Devices Moderate Jan 17, 2024

SoClean 3, REF SC1400, Automated Supplemental Sleep Equipment Maintenance System

SoClean, Inc

FDA Devices Moderate Jan 17, 2024

BIOFIRE FILMARRAY Gastrointestinal (GI) Panel is a qualitative multiplexed nucleic acid-based in vitro diagnostic test intended for use with BIOFIRE …

BioFire Diagnostics, LLC

FDA Devices Moderate Jan 17, 2024

SPRYSTEP VECTOR, Custom made device dynamic ankle-foot orthosis (AFO) , Reference numbers: 17V1030, 17V2030, 17V1031, 17V2031, 17V1032, 17V2032, 17V…

Townsend Design

FDA Devices Moderate Jan 17, 2024

MYNXGRIP 6F/7F, REF MX6721, Vascular Closure Device (VCD). Used to seal femoral arterial and femoral venous access sites

Cordis US Corp

FDA Devices Moderate Jan 17, 2024

Abiomed Introducer Kit, 23 Fr, w/Hlx Vlv Sterile Individual, and Part of Pump Set (004334, 0046-0035, 0052-0002) Part Number: 0052-3021. Intended …

Abiomed, Inc.

FDA Devices Moderate Jan 17, 2024

Baxter Vascular Probe, Product Codes: a) 7081015: 8CM, 1- 1.5 MM GLOBAL, b) 7081520: 8CM, 1.5-2 MM GLOBAL, c) 7082025: 8CM, 2-2.5 MM GLOB…

Baxter Healthcare Corporation

FDA Devices Moderate Jan 17, 2024

Peri-Guard Repair Patch, Product Codes: a) PG1016 : 10 X 16 CMUS, TS b) PG1225: 12 X 25 CMUS, TS c) PG0404: 4 X 4 CMUS, TS d) PG0608: 6 X 8C…

Baxter Healthcare Corporation

FDA Devices Moderate Jan 17, 2024

Abiomed KIT, 14 Fr Introducer, 13 & 25 cm, ABMD Part of Pump Set (0048-0024, 0048-0032)-Introducer(s) are intended for introduction of the Impella Ca…

Abiomed, Inc.

FDA Devices Moderate Jan 17, 2024

Baxter FloSeal Hemostatic Matrix RECOTHROM, Product Codes: a) ADS202105, 5mL-6 PK US b) ADS202110, 10mL US

Baxter Healthcare Corporation

FDA Devices Moderate Jan 17, 2024

Q-Stress Cardiac Stress Testing System, version 6, with below product name / product codes: a) QS6 AM12Q KIT AHA XML / QS6-BXXCS: b) QS6 AM12Q KIT B…

Baxter Healthcare Corporation

FDA Devices Moderate Jan 17, 2024

Model No. ENF-XP, RHINO-LARYNGOFIBERSCOPE

Shirakawa Olympus Co., Ltd.

FDA Devices Moderate Jan 17, 2024

XScribe Cardiac Stress Testing System, version 6, with below product names and codes: a) XS6/RS6 REVIEW WKSTN KIT, XR-6AC-BXXXX; b) XS6/RS6 REVIEW W…

Baxter Healthcare Corporation

FDA Devices Moderate Jan 17, 2024

Peri-Guard Repair Patch, Product Codes: a) PC1016NBIO: 10X16CMUS, b) PC1225NBIO: 12X25CMUS, c) PC0404NBIO: 4X4CMUS, d) PC0608NBIO: 6X8CMUS…

Baxter Healthcare Corporation

FDA Devices Moderate Jan 17, 2024

Bard Mission Disposable Core Biopsy Instrument Kit (REF/Name): 1410MSK/ Mission Kit 14G x 10CM; 1416MSK/ Mission Kit 14G x 16CM; 1610MSK/ Mission Kit…

Bard Peripheral Vascular Inc

NHTSA Critical Jan 15, 2024

KENWORTH 2023: VISIBILITY:REARVIEW MIRRORS/DEVICES

KENWORTH

CPSC Moderate Jan 11, 2024

Alliance4Safety and 31 Furniture Companies Recall Millions of Plastic New Age Furniture Tip-over Restraint Kits Due to Tip-over and Entrapment Hazard…

New Age Industries Co. LTD, of Vietnam

CPSC Moderate Jan 11, 2024

Boot Royalty Recalls Men's Leather Work Boots Due to Crush Hazard

CPSC Moderate Jan 11, 2024

Daikin Comfort Technologies Manufacturing (formerly Goodman Manufacturing Company L.P.) Expands Recall of Evaporator Coil Drain Pans to Include Addit…

Daikin Comfort Technologies Manufacturing L.P. (f/k/a Goodman Manufacturing Company L.P.) of Houston, Texas

CPSC Moderate Jan 11, 2024

Retrospec Recalls Kid's Bike Helmets Due to Risk of Head Injury; Violation of the Federal Safety Regulation for Bicycle Helmets

FDA Food Moderate Jan 10, 2024

Racine Danish Kringles Raspberry Kringle, 14 oz. UPC 0 45251-00312 7. RDK Corp, Racine, WI 53404.

RDK Corp. dba Racine Danish Kringles

FDA Food Critical Jan 10, 2024

Sung Soy Bean Sprouts, 1lb packages, in plastic packages, 20 bags per case

Samsung Bean Sprout

FDA Food Moderate Jan 10, 2024

Scratch PASTA Co MARINARA SAUCE NET WT. 24.5 oz glass jar Ingredients: San Marzano Plum Peeled Tomatoes, Onion, Butter (Cream, Natural Flavor) UPC 8 …

Carolina CoPacking, LLC

FDA Food Moderate Jan 10, 2024

Spring Valley Biotin & Collagen Liquid, Natural Berry Flavor, 15000 mcg, Dietary Supplement 29 doses 1 fl oz (29mL) UPC: 194346065158 Packaged in a g…

BioMylz Pvt. Ltd.

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.