PlainRecalls

2024 Recalls

6,210 recalls · Page 32 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 10 critical, 39 moderate, and 1 lower-severity recalls. The page references 31 distinct recalling firms operating in 6 distinct product categories, with 43 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Devices (31), CPSC (8), NHTSA (7), 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 Sep 25, 2024

ViewPoint 6, Model Numbers: a) H47581RJ, b) H47591MA, c) H47591MT, d) H47591PE, e) H47591PR, f) H47591RA, g) H47591SD, h) H47591YA; system, imaging…

GE Healthcare GmbH

FDA Devices Moderate Sep 25, 2024

2090 Programmers with serial number prefixes PKK0 and PKK1: a) 2090, Product Description: PRGM 2090 PROGRAMMER-PORTABLE CRM; b) 209031, Produc…

Medtronic Inc.

FDA Devices Critical Sep 25, 2024

Baxter EXACTAMIX Inlet, Vented, High Volume Inlet, REF H938174, for use in a pharmaceutical compounding device

Baxter Healthcare Corporation

FDA Devices Moderate Sep 25, 2024

Atellica CH Microalbumin_2 (¿ALB_2)-For in vitro diagnostic use in the quantitative measurement of microalbumin in human urine on ADVIA Chemistry sys…

Siemens Healthcare Diagnostics, Inc.

FDA Devices Moderate Sep 25, 2024

Seer Home System is an ambulatory electroencephalograph (EEG) system intended for at-home use for extended EEG and video EEG (vEEG) recordings and an…

SEER MEDICAL PTY LTD

FDA Devices Critical Sep 25, 2024

Baxter EXACTAMIX Inlet, Vented, Micro-Volume Inlet, REF H938175, for use in a pharmaceutical compounding device

Baxter Healthcare Corporation

FDA Devices Moderate Sep 25, 2024

System Name: 722044 INTEGRIS Allura 15-12 (biplane) 722030 Integris CV Cesar-Powerpack-Visub-Nicol 722021 INTEGRIS Allura 9 (biplane) 722018 Integris…

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

FDA Devices Moderate Sep 25, 2024

Beckman Coulter DxI 9000 Access Immunoassay Analyzer, Model Number C21510, RSM Pneumatic Tubing Kit item #2, REF C11137; in vitro diagnostic instrume…

Beckman Coulter, Inc.

FDA Devices Moderate Sep 25, 2024

regard Clinical Packaging Solutions, HT00376I - SPECIAL PROCEDURE, Item Number 800223009

ROi CPS LLC

FDA Devices Moderate Sep 25, 2024

BinaxNOW Respiratory Strep A Test Kit, CLIA Waived, Catalog Number 730025

Cypress Medical Products LLC

FDA Devices Moderate Sep 25, 2024

ADVIA Chemistry Microalbumin_2 (¿ALB_2) -For in vitro diagnostic use in the quantitative measurement of microalbumin in human urine on ADVIA Chemistr…

Siemens Healthcare Diagnostics, Inc.

FDA Devices Moderate Sep 25, 2024

Flexima Regular Kit Biliary Catheter System Kit, Material Numbers REF M001271650; bile drainage catheter with locking pigtail

Boston Scientific Corporation

FDA Devices Moderate Sep 25, 2024

Acceava Respiratory Strep A, CLIA Waived, Catalog Number 4580295008

Cypress Medical Products LLC

FDA Devices Moderate Sep 25, 2024

System Name: 722059 Allura Xper FD20/15 OR Table 722058 Allura Xper FD20/15 722039 Allura Xper FD20/20 OR Table 722038 Allura Xper FD20/20 722035 All…

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

FDA Devices Moderate Sep 25, 2024

System Name: 708038 MultiDiagnost Eleva with Flat Detector 708037 MultiDiagnost Eleva with Flat Detector 708036 MultiDiagnost Eleva 708034 MultiDiagn…

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

FDA Devices Moderate Sep 25, 2024

DIAMOND POINT, BOTH ENDS K-WIRE, REF 128042, metallic bone fixation fastener

Smith & Nephew, Inc.

FDA Devices Moderate Sep 25, 2024

Marodyne-LiV, part number 3045-133, Low intensity vibration exerciser supporting osteoporosis treatment

Btt Health Gmbh

FDA Devices Low Sep 25, 2024

BiomarC EX Fiducial Marker System, Catalog Number 040165

Carbon Medical Technologies, Inc.

FDA Devices Moderate Sep 25, 2024

Mazor X. Model Number REF TPL0059; stereotaxic orthopedic instrument

Mazor Robotics Ltd

FDA Devices Moderate Sep 25, 2024

STREAMLINE BLOODLINE LONG VERSION, FMC-Tubing to be used to transfer blood between a patient and a haemodialyser during haemodialysis. Model/Catal…

B Braun Medical Inc

FDA Devices Moderate Sep 25, 2024

Alaris Syringe Module Model 8110, a modular infusion pump and monitoring system

CareFusion 303, Inc.

FDA Devices Critical Sep 25, 2024

Baxter EXACTAMIX Inlet, Non-Vented, High Volume Inlet, REF H938173, for use in a pharmaceutical compounding device

Baxter Healthcare Corporation

FDA Devices Moderate Sep 25, 2024

ERIC Retrieval Device REF: ER173020 ER174030 ER176044 The ERIC Retrieval Device is a mechanical thrombectomy device designed to restore blood …

MICROVENTION INC.

FDA Devices Moderate Sep 25, 2024

1. Tech Medical Services Inc. Detachable Endo Retrieval Pouch, REF TM2001, 3" x 6", sterile; 2. Tech Medical Services Inc. Detachable Endo Retrie…

UNIMAX MEDICAL SYSTEMS INC

FDA Devices Moderate Sep 25, 2024

DIAMOND POINT, BOTH ENDS K-WIRE, REF 128062, metallic bone fixation fastener

Smith & Nephew, Inc.

FDA Devices Moderate Sep 25, 2024

AET36 ANESTH EXT SET - Anesthesia Extension Set - Normally Closed Dual Manifold, Four-way Stopcock, Model/Catalog Number: 472036

B. Braun Medical, Inc.

FDA Devices Moderate Sep 25, 2024

General Purpose Syringe McKesson 60 mL Luer Lock Tip Without Safety, Catalog Number 869662, McKesson Brand Catalog Number: 102-S60C

Cypress Medical Products LLC

FDA Devices Moderate Sep 25, 2024

STREAMLINE BLOODLINE SET FOR DIALOG DR-Tubing to be used to transfer blood between a patient and a haemodialyser during haemodialysis. Model/Catal…

B Braun Medical Inc

FDA Devices Moderate Sep 25, 2024

Flexima APDL Drainage Catheter System and Kit, Material Numbers: a) REF M001271960, b) REF M001271970; all-purpose drainage catheter with locking pi…

Boston Scientific Corporation

FDA Devices Moderate Sep 25, 2024

GE Healthcare Centricity Universal Viewer Zero Footprint Client, Model Numbers: a) 2110344-008; b) 2110344-009; c) 2110344-010; d) 2110344-…

GE Healthcare

FDA Devices Moderate Sep 25, 2024

ViewPoint; system, imaging processing, radiological

GE Healthcare GmbH

NHTSA Critical Sep 25, 2024

BMW,MINI 2023-2025: STRUCTURE:BODY

BMW,MINI

NHTSA Critical Sep 25, 2024

BUICK 2024: EQUIPMENT:OTHER:LABELS

BUICK

NHTSA Critical Sep 24, 2024

ASTON MARTIN 2025: ENGINE AND ENGINE COOLING:ENGINE:OIL/LUBRICATION:PIPES, HOSES, AND FITTINGS

ASTON MARTIN

NHTSA Critical Sep 20, 2024

TOYOTA 2023-2025: SERVICE BRAKES, ELECTRIC:SOFTWARE/PROGRAMMING

TOYOTA

NHTSA Critical Sep 20, 2024

MERCEDES-BENZ 2021-2023: ENGINE AND ENGINE COOLING:ENGINE:ENGINE CONTROL MODULE (ECU/ECM):SOFTWARE

MERCEDES-BENZ

CPSC Moderate Sep 19, 2024

Caframo Cabinet Heaters Recalled Due to Electrocution Hazard; Manufactured by Caframo Limited

Caframo Limited, of Canada

CPSC Moderate Sep 19, 2024

Ceither Adult Portable Bed Rails Recalled Due to Serious Entrapment and Asphyxia Hazards; Violation of Federal Regulations for Adult Portable Bed Rai…

Yangkeqiang, dba Inforce, of China

CPSC Moderate Sep 19, 2024

Children's Jewelry Sets Recalled Due to Risk of Lead and Cadmium Poisoning; Violations of the Federal Lead Content Ban and Federal Hazardous Substanc…

CPSC Moderate Sep 19, 2024

CVB Recalls LUCID Platform Beds with Upholstered Square Tufted Headboards Due to Fall and Injury Hazards

CPSC Moderate Sep 19, 2024

Jo-Ann Stores Recalls Place & Time Battery-Operated Desk Lamps Due to Fire Hazard

CPSC Moderate Sep 19, 2024

Polaris Industries Recalls Ranger XD 1500 Recreational Off-Road Vehicles (ROVs) with Winches Due to Fire Hazard

Polaris Industries Inc., of Medina, Minnesota

CPSC Moderate Sep 19, 2024

Polaris Recalls Sportsman All-Terrain Vehicles Due to Fire Hazard

Polaris Industries Inc., of Medina, Minnesota

CPSC Moderate Sep 19, 2024

Wee Gallery Recalls Baby Tummy Time Gallery Due to Violation of the Federal Phthalates Ban

NHTSA Critical Sep 19, 2024

CHEVROLET,GMC 2023-2024: SEAT BELTS:CRITICAL FASTENERS

CHEVROLET,GMC

NHTSA Critical Sep 19, 2024

CHEVROLET,GMC 2013-2019: SERVICE BRAKES, HYDRAULIC:POWER ASSIST:HYDRAULIC:HOSES, LINES/PIPING, AND FITTINGS

CHEVROLET,GMC

FDA Food Moderate Sep 18, 2024

American Outdoor Products - Astronaut Strawberries, packaged in 0.5oz (14g) metallic plastic pouches. Sold individually or in 6, 12, 40, or 160 count…

American Outdoor Products, Inc.

FDA Food Moderate Sep 18, 2024

UPC 71117 14743, Reser s Rotisserie Chicken Salad Base 2lb. (32oz), refrigerated, packaged in an opaque plastic tub with a white printed plastic lid.…

Reser's Fine Foods, Inc.

FDA Food Moderate Sep 18, 2024

UPC 71117 19063, Reser's American Classics Garden Pasta Salad 16oz, refrigerated, packaged in an opaque printed plastic tub with a plastic red printe…

Reser's Fine Foods, Inc.

FDA Food Moderate Sep 18, 2024

UPC 78742 12653, Walmart Original Freshness Guaranteed Macaroni Salad 16oz, refrigerated, packaged in a clear plastic tub with printed labels on top,…

Reser's Fine Foods, 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 July 2026.