PlainRecalls

2024 Recalls

4,937 recalls · Page 65 of 99

2024 Recall Year Insight

Federal agencies issued 4,937 product recalls indexed by PlainRecalls in calendar year 2024. That represents about 5.88% of the 83,949 total recalls we track from 1995 through the present, and averages roughly 13.5 recalls per day across the FDA, CPSC, NHTSA, and USDA FSIS 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 99 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 1 critical, 49 moderate, and 0 lower-severity recalls. The page references 20 distinct recalling firms operating in 5 distinct product categories, with 34 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Devices (39), CPSC (10), NHTSA (1), 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, NHTSA, or USDA FSIS for the system-of-record on any specific recall. PlainRecalls indexes this archive for research and consumer awareness purposes.

FDA Devices Moderate May 8, 2024

IPS e.max ZirCAD CER/in. Prime C2 C17/5- A zirconium oxide block for the fabrication of fixed, full-contour restorations in anterior and posterior t…

IVOCLAR VIVADENT AG

FDA Devices Moderate May 8, 2024

Jackson-Pratt Universal Connector PVC Tubing Anti Reflux Transparent Y, REF SU130-4601

Cardinal Health 200, LLC

FDA Devices Moderate May 8, 2024

ZPLP(Zimmer Periarticular Locking Plate System) Distal Lateral Fibular Plate, Left, 6 Holes, 106 MM, Sterile- Indicated for temporary internal fixat…

Zimmer, Inc.

FDA Devices Moderate May 8, 2024

RayStation 9.0.0.113 and 9.0.1.142. Radiation Therapy Treatment Planning System.

RAYSEARCH LABORATORIES AB

FDA Devices Moderate May 8, 2024

Jackson-Pratt 3-Spring Reservoir Kit with PVC Round Drain, 400mL, 10Fr., REF SU130-402D

Cardinal Health 200, LLC

FDA Devices Moderate May 8, 2024

Galaxy System REF GAL-001 (specifically GAL-019, Wired Controller) The Galaxy System and its accessories are intended to provide bronchoscopic vis…

Noah Medical

FDA Devices Moderate May 8, 2024

ZPLP Distal Lateral Fibular Plate, Right, 6 Holes, 106 MM, Nonsterile- Indicated for temporary internal fixation and stabilization of osteotomies and…

Zimmer, Inc.

FDA Devices Moderate May 8, 2024

ZPLP (Zimmer Periarticular Locking Plate System) Distal Lateral Fibular Plate, Left, 16 Holes, 236 MM, Sterile- Indicated for temporary internal fixa…

Zimmer, Inc.

FDA Devices Moderate May 8, 2024

ZPLP Distal Lateral Fibular Plate, Left, 14 Holes, 210 MM, Sterile- Indicated for temporary internal fixation and stabilization of osteotomies and fr…

Zimmer, Inc.

FDA Devices Moderate May 8, 2024

RayStation 11.0.0.951, 11.0.1.29, 11.0.3.116 & 11.0.4.15. Radiation Therapy Treatment Planning System.

RAYSEARCH LABORATORIES AB

FDA Devices Moderate May 8, 2024

ZPLP (Zimmer Periarticular Locking Plate System) Distal Lateral Fibular Plate, Right, 6 Holes, 106 MM, Sterile- Indicated for temporary internal fix…

Zimmer, Inc.

FDA Devices Moderate May 8, 2024

ZPLP Distal Lateral Fibular Plate, Right, 8 Holes, 132 MM, Nonsterile- Indicated for temporary internal fixation and stabilization of osteotomies and…

Zimmer, Inc.

FDA Devices Moderate May 8, 2024

RayStation 8.0.0.61, 8.0.1.10. Radiation Therapy Treatment Planning System.

RAYSEARCH LABORATORIES AB

FDA Devices Moderate May 8, 2024

Jackson-Pratt 3-Spring Reservoir with Silicone Adapters, 400mL, REF SU130-475

Cardinal Health 200, LLC

FDA Devices Moderate May 8, 2024

IPS e.max ZirCAD CER/in. Prime A3 C17/5 -A zirconium oxide block for the fabrication of fixed, full-contour restorations in anterior and posterior t…

IVOCLAR VIVADENT AG

FDA Devices Moderate May 8, 2024

OsmoPRO MAX Automated Osmometer- IVD Osmometer for Clinical Use. Uses the method of freezing point depression to measure osmolality of serum, plasma,…

Advanced Instruments, LLC

FDA Devices Moderate May 8, 2024

The Oncology Essentials Package of the Spectral CT imaging system.

Philips North America Llc

FDA Devices Moderate May 8, 2024

ZPLP Distal Lateral Fibular Plate, Left, 6 Holes, 106 MM, Nonsterile- Indicated for temporary internal fixation and stabilization of osteotomies and …

Zimmer, Inc.

FDA Devices Moderate May 8, 2024

ZPLP (Zimmer Periarticular Locking Plate System) Distal Lateral Fibular Plate, Left, 8 Holes, 132 MM, Sterile- Indicated for temporary internal fixat…

Zimmer, Inc.

FDA Devices Moderate May 8, 2024

ZPLP (Zimmer Periarticular Locking Plate System) Distal Lateral Fibular Plate, Right, 12 Holes, 184 MM, Sterile- Indicated for temporary internal fix…

Zimmer, Inc.

FDA Devices Moderate May 8, 2024

RayStation 15.0.0.430. Radiation Therapy Treatment Planning System.

RAYSEARCH LABORATORIES AB

FDA Devices Moderate May 8, 2024

The Distal Access Catheter is a single-lumen, braided shaft, variable stiffness catheter with radiopaque marker on the distal end and a luer hub on t…

Stryker Neurovascular

FDA Devices Moderate May 8, 2024

ZPLP (Zimmer Periarticular Locking Plate System) Distal Lateral Fibular Plate, Right, 4 Holes, 80 MM, Sterile- Indicated for temporary internal fixat…

Zimmer, Inc.

FDA Devices Moderate May 8, 2024

Battery Mobile X-ray Unit EASY MOVING Model with telescopic column 3.1, model numbers: a. SM-20HF-Batt; b. SM-32HF-Batt; c. SM-40HF-Batt; d.…

SEDECAL SA

FDA Devices Moderate May 8, 2024

Keller Funnel 2, REF: HA-001, STERILEEO, Rx Only,

Allergan Sales, LLC

FDA Devices Moderate May 8, 2024

ZPLP Distal Lateral Fibular Plate, Left, 4 Holes, 80 MM, Nonsterile- Indicated for temporary internal fixation and stabilization of osteotomies and f…

Zimmer, Inc.

FDA Devices Moderate May 8, 2024

RayStation 7.0.0.19. Radiation Therapy Treatment Planning System.

RAYSEARCH LABORATORIES AB

FDA Devices Moderate May 8, 2024

POWERSEAL 5 mm, 44 cm, Curved Jaw Sealer and Divider, Double Action is indicated for use in general surgery and such surgical specialties as urologic…

Olympus Corporation of the Americas

FDA Devices Moderate May 8, 2024

Medtronic Invos, Reusable Sensor Cable for PM7100, REF: PMAC71RSC

Covidien

FDA Devices Moderate May 8, 2024

IPS e.max ZirCAD CER/in. Prime BL1 C17/3- A zirconium oxide block for the fabrication of fixed, full-contour restorations in anterior and posterior …

IVOCLAR VIVADENT AG

FDA Devices Moderate May 8, 2024

RayStation 10.0.0.1154, 10.0.1.52 & 10.0.2.10. Radiation Therapy Treatment Planning System.

RAYSEARCH LABORATORIES AB

FDA Devices Moderate May 8, 2024

ZPLP (Zimmer Periarticular Locking Plate System) Distal Lateral Fibular Plate, Left, 12 Holes, 184 MM, Sterile- Indicated for temporary internal fix…

Zimmer, Inc.

FDA Devices Moderate May 8, 2024

ZPLP (Zimmer Periarticular Locking Plate System) Distal Lateral Fibular Plate, Right, 10 Holes, 158 MM, Sterile- Indicated for temporary internal fix…

Zimmer, Inc.

FDA Devices Moderate May 8, 2024

ZPLP(Zimmer Periarticular Locking Plate System) Distal Lateral Fibular Plate, Left, 10 Holes, 158 MM, Sterile- Indicated for temporary internal fixa…

Zimmer, Inc.

FDA Devices Moderate May 8, 2024

Jackson-Pratt 3-Spring Reservoir Kit with PVC Round Drain, 400mL, 15Fr., REF SU130-403D

Cardinal Health 200, LLC

FDA Devices Moderate May 8, 2024

RayStation 10.1.0.613 and 10.1.1.54. Radiation Therapy Treatment Planning System.

RAYSEARCH LABORATORIES AB

FDA Devices Moderate May 8, 2024

ADVANCED RESEARCH MEDICAL Lumbar Interbody Fusion System (OLLIF), Flexible Curette Loop Blade, Part # 01-06-4; treatment of degenerative disc disease

Advanced Research Medical, LLC

FDA Devices Moderate May 8, 2024

IPS e.max ZirCAD CER/in. Prime A2 C17/5 -A zirconium oxide block for the fabrication of fixed, full-contour restorations in anterior and posterior t…

IVOCLAR VIVADENT AG

FDA Devices Moderate May 8, 2024

ZPLP Distal Lateral Fibular Plate, Left, 10 Holes, 158 MM, Nonsterile-Indicated for temporary internal fixation and stabilization of osteotomies and …

Zimmer, Inc.

CPSC Moderate May 2, 2024

American Honda Motor Expands Recall of Lawnmowers and Pressure Washer Engines to include Lawnmower Replacement Engines Due to Injury Hazard; Addition…

American Honda Motor Co. Inc., of Torrance, California

CPSC Moderate May 2, 2024

Arctic Cat Recalls Snowmobiles Due to Laceration Hazard

Arctic Cat, of Thief River Falls, Minnesota

CPSC Moderate May 2, 2024

Bausch + Lomb Recalls Project Watson Eyelid Wipes for Dogs Due to Risk of Exposure to Bacteria and Fungi

Bausch & Lomb Americas Inc., of Bridgewater, New Jersey

CPSC Moderate May 2, 2024

Children's Dressers Sold Exclusively at Rooms To Go Recalled Due to Tip-Over and Entrapment Hazards; Violation of Federal Regulation for Clothing Sto…

CPSC Moderate May 2, 2024

Dixon Ticonderoga Recalls Creativity Street Foam Pattern Rollers Due to Violation of Federal Lead Content Ban

CPSC Moderate May 2, 2024

DR Power Equipment Recalls Leaf Blowers and Leaf Vacuums Due to Laceration Hazard

Generac Power Systems Inc., of Waukesha, Wisconsin

CPSC Moderate May 2, 2024

Igloo Products Recalls Youth Sipper Bottles Due to Choking Hazard

CPSC Moderate May 2, 2024

Polaris Recalls Prostar S4 Titan Adventure Snowmobiles Due to Fire Hazard

Polaris Industries Inc., of Medina, Minnesota

CPSC Moderate May 2, 2024

Skims Body Recalls SKIMS Children's Pajama Sets Due to Burn Hazard; Violation of Federal Regulations for Children's Sleepwear; Sold Exclusively by Sk…

CPSC Moderate May 2, 2024

True Manufacturing Recalls Commercial Refrigerators with Secop Compressors Due to Fire Hazard

Secop GmbH, of Germany (compressors

NHTSA Critical May 2, 2024

CADILLAC 2024: AIR BAGS:FRONTAL

CADILLAC

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 + USDA FSIS — consumer product, vehicle, and meat/poultry recall feeds for 2024