PlainRecalls

2024 Recalls

6,210 recalls · Page 47 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 12 critical, 37 moderate, and 1 lower-severity recalls. The page references 29 distinct recalling firms operating in 7 distinct product categories, with 42 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Devices (33), NHTSA (7), CPSC (6), 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 21, 2024

WAVEWRITER ALPHA: Model: SC-1216, 16 IPG KIT, REF: M365SC12160; Model: SC-1232, 32 IPG KIT, REF: M365SC12320

Boston Scientific Neuromodulation Corporation

FDA Devices Moderate Aug 21, 2024

Various Merit Medical convenience kits that contain recalled Jiangsu Shenli Medical Production Co. Ltd. syringes: K11 (Custom Pressure Monitoring …

Merit Medical Systems, Inc.

FDA Devices Moderate Aug 21, 2024

Orthopantomograph OP300 dental computed tomography x-ray system. The X-ray device produces conventional 2D X-ray images and Xray projection image…

Palodex Group Oy

FDA Devices Moderate Aug 21, 2024

Various Merit Medical convenience kits that contain recalled Jiangsu Shenli Medical Production Co. Ltd. syringes: Safety Paracentesis Procedure Tr…

Merit Medical Systems, Inc.

FDA Devices Moderate Aug 21, 2024

Various Merit Medical convenience kits that contain recalled Jiangsu Shenli Medical Production Co. Ltd. syringes: Customer Procedure Kit (Angiogra…

Merit Medical Systems, Inc.

FDA Devices Moderate Aug 21, 2024

Various Merit Medical convenience kits that contain recalled Jiangsu Shenli Medical Production Co. Ltd. syringes: K04 (Custom Syringe Kit), REF: …

Merit Medical Systems, Inc.

FDA Devices Moderate Aug 21, 2024

Various Merit Medical convenience kits that contain recalled Jiangsu Shenli Medical Production Co. Ltd. syringes: Customer Procedure Kit (Angiography…

Merit Medical Systems, Inc.

FDA Devices Moderate Aug 21, 2024

Brand Name: UNclog Eye Mask Product Name: UNclog Eye Mask Model/Catalog Number: AG23JW24 Serial # ag22 Product Description: Heated eye mask Compo…

EYE COMFORT CARE LLC

FDA Devices Critical Aug 21, 2024

RMU-2000 Automated Chest Compression Device

Defibtech, LLC

FDA Devices Moderate Aug 21, 2024

Various Merit Medical convenience kits that contain recalled Jiangsu Shenli Medical Production Co. Ltd. syringes: ReSolve (Catheter and Tip Suctio…

Merit Medical Systems, Inc.

FDA Devices Moderate Aug 21, 2024

VITROS Immunodiagnostic VITROS Folate Reagent Pack 1/2

Ortho-Clinical Diagnostics, Inc.

FDA Devices Moderate Aug 21, 2024

Various Merit Medical convenience kits that contain recalled Jiangsu Shenli Medical Production Co. Ltd. syringes: K12T/12PI (Custom Pressure Monit…

Merit Medical Systems, Inc.

FDA Devices Moderate Aug 21, 2024

Aurora Series, Aurora 7 lighthead; Models: LED7 (including TV models). The Aurora Series is intended to illuminate the surgical field and ensure vi…

DKK Dai-Ichi Shomei Co., Ltd.

FDA Devices Moderate Aug 21, 2024

Various Merit Medical convenience kits that contain recalled Jiangsu Shenli Medical Production Co. Ltd. syringes: Custom Procedure Kit (Angiograph…

Merit Medical Systems, Inc.

FDA Devices Moderate Aug 21, 2024

Various Merit Medical convenience kits that contain recalled Jiangsu Shenli Medical Production Co. Ltd. syringes: K10/K10-PI (Custom Waste Managem…

Merit Medical Systems, Inc.

FDA Devices Moderate Aug 21, 2024

HeartMate 3 System Controllers provided within the following HeartMate 3 Left Ventricular Assist System (LVAS) Implant Kits or distributed separately…

Thoratec LLC

FDA Devices Moderate Aug 21, 2024

L-CATH PICC S/L Peripherally Inserted Central Catheter, 26Ga (1.9F) 0.60mm x 30cm, REF: 384539

Argon Medical Devices, Inc

FDA Devices Critical Aug 21, 2024

Plum 360/A+ spare batteries. Item Number: SUB0000864.

ICU Medical Inc

FDA Devices Moderate Aug 21, 2024

Aurora 4 Series, Aurora 7 lighthead; Models: AUA7 (including TV models). The Aurora Series is intended to illuminate the surgical field and ensure v…

DKK Dai-Ichi Shomei Co., Ltd.

FDA Devices Moderate Aug 21, 2024

Various Merit Medical convenience kits that contain recalled Jiangsu Shenli Medical Production Co. Ltd. syringes: K08-PI (Custom Fluid Management …

Merit Medical Systems, Inc.

FDA Devices Critical Aug 21, 2024

Replacement Battery List Number SUB0000864, found in Plum 360 Infusion System, List Number 30010. Product description is PLUM 360 Infuser. OUS uni…

ICU Medical Inc

FDA Devices Moderate Aug 21, 2024

Aurora 3 Series, Aurora 7 lighthead; Models: AUT7 (including TV models). The Aurora Series is intended to illuminate the surgical field and ensure v…

DKK Dai-Ichi Shomei Co., Ltd.

FDA Devices Moderate Aug 21, 2024

Beckman Coulter DxI 9000 Access Immunoassay Analyzer, Catalog #C11137.

Beckman Coulter, Inc.

FDA Devices Moderate Aug 21, 2024

Various Merit Medical convenience kits that contain recalled Jiangsu Shenli Medical Production Co. Ltd. syringes: Prelude Prestige (Introducer Cat…

Merit Medical Systems, Inc.

FDA Devices Moderate Aug 21, 2024

Aurora 2 Series, Aurora 7 lighthead; Models: AUR7 (including TV models). The Aurora Series is intended to illuminate the surgical field and ensure vi…

DKK Dai-Ichi Shomei Co., Ltd.

FDA Devices Moderate Aug 21, 2024

BD Kiestra Urine Culture Application Powered by BD Synapsys Informatics Solution; Catalog (Ref): 444900;

Becton Dickinson & Co.

FDA Devices Moderate Aug 21, 2024

Various Merit Medical convenience kits that contain recalled Jiangsu Shenli Medical Production Co. Ltd. syringes: K02 (Custom Syringe Kit), REF: …

Merit Medical Systems, Inc.

FDA Devices Moderate Aug 21, 2024

Various Merit Medical convenience kits that contain recalled Jiangsu Shenli Medical Production Co. Ltd. syringes: SafeSheath CSG/Worley advanced C…

Merit Medical Systems, Inc.

FDA Devices Moderate Aug 21, 2024

Various Merit Medical convenience kits that contain recalled Jiangsu Shenli Medical Production Co. Ltd. syringes: Outake, REF CET200 and CET300, …

Merit Medical Systems, Inc.

FDA Devices Moderate Aug 21, 2024

Various Merit Medical convenience kits that contain recalled Jiangsu Shenli Medical Production Co. Ltd. syringes: Prelude SNAP-H (Introducer Cathe…

Merit Medical Systems, Inc.

FDA Devices Moderate Aug 21, 2024

BioButton REF BIOST06040 with Software version 3.0.20 The BioButton System is a remote monitoring wearable device intended for continuous collecti…

Biointellisense Inc.

FDA Devices Moderate Aug 21, 2024

Various Merit Medical convenience kits that contain recalled Jiangsu Shenli Medical Production Co. Ltd. syringes: SafeSheath CSG (Introducer Cathe…

Merit Medical Systems, Inc.

FDA Devices Moderate Aug 21, 2024

Various Merit Medical convenience kits that contain recalled Jiangsu Shenli Medical Production Co. Ltd. syringes: Custom Procedure Kit (Angiograph…

Merit Medical Systems, Inc.

NHTSA Critical Aug 21, 2024

CHEVROLET 2024: TRAILER HITCHES

CHEVROLET

NHTSA Critical Aug 20, 2024

FISKER 2023: SERVICE BRAKES, ELECTRIC:SOFTWARE/PROGRAMMING

FISKER

NHTSA Critical Aug 19, 2024

AUDI 2019: SERVICE BRAKES, HYDRAULIC:PEDALS AND LINKAGES

AUDI

CPSC Moderate Aug 15, 2024

ALDI Recalls Ambiano Single Serve Coffee Makers Due to Burn Hazard

CPSC Moderate Aug 15, 2024

BJ's Wholesale Club Recalls Berkley Jensen Gazebos Due to Injury Hazard (Recall Alert)

Lypometal Sdn. Bhd., of Malaysia (Sunjoy Group)

CPSC Moderate Aug 15, 2024

IKEA Recalls VARMFRONT Power Banks Due to Fire Hazard

IKEA US Retail LLC, of Glen Allen, Virginia

CPSC Moderate Aug 15, 2024

Mamibaby and Cosy Nation Baby Loungers Recalled Due to Suffocation Risk and Fall and Entrapment Hazards; Violation of Federal Regulations for Infant …

Hangzhoumeixiajianzhushejiyouxiangongs D/B/A MEIXIA Shop, of China

CPSC Moderate Aug 15, 2024

Stanley Black & Decker Recalls DeWALT Battery Walk-Behind Mowers Due to Laceration Hazard

Stanley Black and Decker Inc., of New Britain, Connecticut

CPSC Moderate Aug 15, 2024

Trader Joe's Company Recalls Mango Tangerine Scented Candles Due to Fire Hazard

Trader Joe's Company, of Monrovia, California

NHTSA Critical Aug 15, 2024

TESLA 2016: STRUCTURE:BODY

TESLA

NHTSA Critical Aug 15, 2024

ACURA 2024: SERVICE BRAKES, HYDRAULIC:ANTILOCK/TRACTION CONTROL/ELECTRONIC LIMITED SLIP:CONTROL UNIT/MODULE

ACURA

NHTSA Critical Aug 15, 2024

MINI 2022-2023: ELECTRICAL SYSTEM:PROPULSION SYSTEM:TRACTION BATTERY THERMAL:MANAGEMENT:SOFTWARE

MINI

NHTSA Critical Aug 15, 2024

BMW 2024: STRUCTURE:FRAME AND MEMBERS

BMW

FDA Food Critical Aug 14, 2024

1. Palmer Candy Drizzled Caramel Corn, Item 19271, Net Wt. 16/5oz tubs, UPC 77343 19271 2. Meijer Drizzled Caramel Popcorn Snack Bowl, Net Wt. 12oz, …

Palmer & Company

FDA Food Low Aug 14, 2024

Lemon Drop Mixer is a non-alcoholic cocktail mixer. Product is packaged in glass 750ml bottle and sold under brand Urban River Spirits. Label has li…

Urban River Spirits

FDA Food Moderate Aug 14, 2024

Izzio Everything Roll packaged in 12oz plastic bag, 6 rolls per bag - 16 bags per case.

Izzio Artisan Bakery, LLC

FDA Food Critical Aug 14, 2024

Wiers Farm - Hungarian Wax Peppers packaged into 1lb carton - cases size dependent on customer

Wiers Farm 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.