2024 Recalls

Compiled from official public sources by the editorial team. · Updated August 2026

6,210 recalls · Page 111 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 25 critical, 25 moderate, and 0 lower-severity recalls. The page references 31 distinct recalling firms operating in 7 distinct product categories, with 25 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Devices (18), NHTSA (15), FDA Food (11), 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.

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FDA Devices Critical Feb 14, 2024

Cardinal Health Monoject, 3 mL Purple Enteral Syringe with Enfit Connection Sterile, REF 403SE

Cardinal Health 200, LLC

FDA Devices Moderate Feb 14, 2024

Neurovascular embolization device. The Optima Coil System is a series specialized coils that are inserted into the vasculature under angiographic vis…

BALT USA, LLC

FDA Devices Moderate Feb 14, 2024

HRIS ACET CUP CUT TIP 32X140 Part Number: 6210-5-200rker. single-use, sterile surgical instruments used during hip arthroplasty

Howmedica Osteonics Corp.

FDA Devices Moderate Feb 14, 2024

BD BBL Sensi Disc Ceftriaxone- 30 ug, used for semi-quantitative in vitro susceptibility testing. Catalog Number 231634 and 231635¿

Becton Dickinson & Co.

FDA Devices Moderate Feb 14, 2024

Total immunoglobulin M (IgM total) IVD, kit, nephelometry/turbidimetry

Siemens Healthcare Diagnostics, Inc.

FDA Devices Moderate Feb 14, 2024

The Prestige Coil System is a product family of embolic coils with associated delivery system components. These devices are angiographically delivere…

BALT USA, LLC

FDA Devices Moderate Feb 14, 2024

Ingenia Elition X (Product Number 781358) - HA FlexTrak II (Accessory Number 989710008732), patient transportation system

Philips North America

FDA Devices Moderate Feb 14, 2024

BEQ-RF-32-USA RotaFlow Centrifugal Pump with BIOLINE Coating, Product Code 701047554. For use with an extracorporeal cardiovascular or cardiopulmonar…

Maquet Medical Systems USA

FDA Devices Moderate Feb 14, 2024

BD BBL Sensi Disc Doripenem- 15 ug, used for semi-quantitative in vitro susceptibility testing. Catalog Number 232219¿

Becton Dickinson & Co.

FDA Devices Moderate Feb 14, 2024

BD BBL Sensi Disc Ampicillin with Sulbactam 10/10 ¿g, Catalog Number 231660. Used for semi-quantitative in vitro susceptibility testing.

Becton Dickinson & Co.

FDA Devices Moderate Feb 14, 2024

BD BBL Sensi Disc Clarithromycin- 15 ug, used for semi-quantitative in vitro susceptibility testing. Catalog Number 231678¿

Becton Dickinson & Co.

FDA Devices Critical Feb 14, 2024

Children's Bathrobes Recalled Due to Burn Hazard and Violation of Flammability Regulations; Sold by Nanchang Zhongcangjishi E-commerce

Nanchang Zhongcangjishi E-commerce Co. Ltd, of China

CPSC Moderate Feb 8, 2024

Electrolux Group Recalls Frigidaire Side by Side Refrigerators with Slim Ice Buckets Due to Choking and Laceration Hazards

CPSC Moderate Feb 8, 2024