PlainRecalls

2025 Recalls

6,168 recalls · Page 106 of 124

2025 Recall Year Insight

Federal agencies issued 6,168 product recalls indexed by PlainRecalls in calendar year 2025. That represents about 6.06% of the 101,704 total recalls we track from 1995 through the present, and averages roughly 16.9 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 124 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 2025.

On this page of 50 records, severity classification shows 21 critical, 29 moderate, and 0 lower-severity recalls. The page references 17 distinct recalling firms operating in 6 distinct product categories, with 47 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Devices (42), CPSC (5), NHTSA (3), 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 2025 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 Feb 26, 2025

Brand Name: RayStation- Intended as a Radiation Therapy Treatment Planning System Model/Catalog Number: 10.1.0.613 and 10.1.1.54 Software Version: …

RAYSEARCH LABORATORIES AB

FDA Devices Moderate Feb 26, 2025

AnchorFast SlimFit, Oral Endotracheal Tube Fastener, REF 9787,

Hollister Incorporated

FDA Devices Moderate Feb 26, 2025

AnchorFast, Oral Endotracheal Tube Fastener, REF 9799,

Hollister Incorporated

FDA Devices Moderate Feb 26, 2025

Hot Dog PATIENT WARMING, Underbody Warming Mattress + Return Electrode, 127 cm (50"), REF US502, to prevent or treat hypothermia

Augustine Temperature Management, LLC

FDA Devices Critical Feb 26, 2025

Azurion 7 M20; Catalog numbers: (1) 722079, (2) 722224, (3) 722234, (4) 722282 (OUS ONLY);

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

FDA Devices Critical Feb 26, 2025

Intact Vascular Tack Endovascular System, to treat vascular dissections with Tack implant(s) following angioplasty: (4F,1.5-4.5mm), 150cm, REF: 15415…

Spectranetics Corporation

FDA Devices Moderate Feb 26, 2025

Medline Convenience Kits for Various Procedures: 1) ADULT INTUBATION TRAY, Model Number DYNJAA254A; 2) ADULT MAIN DISP. INTUB PART A, Model Number …

MEDLINE INDUSTRIES, LP - Northfield

FDA Devices Critical Feb 26, 2025

Azurion 3 M12; Catalog numbers: (1) 722063, (2) 722221.

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

FDA Devices Moderate Feb 26, 2025

Brand Name: RayStation- Intended as a Radiation Therapy Treatment Planning System Model/Catalog Number: 4.5.1.14, 4.7.2.5, 4.7.3.13, 4.7.4.4, 4.7.5.…

RAYSEARCH LABORATORIES AB

FDA Devices Moderate Feb 26, 2025

Hot Dog PATIENT WARMING, Underbody Warming Mattress + Return Electrode, 82 cm (32"), REF US501, to prevent or treat hypothermia

Augustine Temperature Management, LLC

FDA Devices Critical Feb 26, 2025

Allura Xper FD20; Catalog numbers: (1) 722006, (2) 722012, (3) 722028.

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

FDA Devices Critical Feb 26, 2025

Allura Xper FD20 Biplane OR Table; Catalog numbers: (1) 722020, (2) 722025.

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

FDA Devices Moderate Feb 26, 2025

Irix-A Integrated Lumbar Fusion System, Model Number X080-423011-08PC (Spacer Assy, 42 X 30 X 8¿, 11mm, PC (STERILE)) and Model Number X080-382819-08…

XTANT Medical Holdings, Inc

FDA Devices Moderate Feb 26, 2025

Medline RR-LIVER TRNS ACCESSORY PEDS, DUNJ63397; medical procedure convenience kit

MEDLINE INDUSTRIES, LP - Northfield

FDA Devices Moderate Feb 26, 2025

Brand Name: RayStation Intended as a Radiation Therapy Treatment Planning System. Model/Catalog Number: 7.0.0.19, 8.0.0.61, 8.0.1.10 Software Ver…

RAYSEARCH LABORATORIES AB

FDA Devices Moderate Feb 26, 2025

AnchorFast Guard Select, Oral Endotracheal Tube Fastener, REF 9700,

Hollister Incorporated

FDA Devices Moderate Feb 26, 2025

Brand Name: RayStation -Intended as a Radiation Therapy Treatment Planning System Model/Catalog Number: 9.1.0.933, 9.2.0.483, 10.0.0.1154, 10.0.1.…

RAYSEARCH LABORATORIES AB

FDA Devices Moderate Feb 26, 2025

Brand Name: RayStation- Intended as a Radiation Therapy Treatment Planning System Model/Catalog Number: 6.1.1.2, 6.2.0.7, 6.3.0.6 Software Version:…

RAYSEARCH LABORATORIES AB

FDA Devices Critical Feb 26, 2025

Allura Xper FD20/15; Catalog numbers: 722058

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

FDA Devices Critical Feb 26, 2025

Azurion 5 M12; Catalog numbers: (1) 722227, (2) 722231 (OUS ONLY).

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

FDA Devices Critical Feb 26, 2025

Allura Xper FD20 OR Table; Catalog numbers: (1) 722023, (2) 722035.

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

FDA Devices Moderate Feb 26, 2025

Augustine Surgical Inc. HotDog Return Electrode accessory connector cables, Model A138 used in conjunction with Warming Blankets and Mattresses.

Augustine Temperature Management, LLC

FDA Devices Critical Feb 26, 2025

Azurion 7 B20; Catalog numbers: (1) 722068, (2) 722226, (3) 722236.

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

FDA Devices Critical Feb 26, 2025

Azurion 7 B12; Catalog numbers: (1) 722067, (2) 722225, (3) 722235 (OUS ONLY).

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

FDA Devices Moderate Feb 26, 2025

AnchorFast Guard, Oral Endotracheal Tube Fastener, REF 9800,

Hollister Incorporated

FDA Devices Critical Feb 26, 2025

Azurion 7 M12; Catalog numbers: (1) 722078, (2) 722223, (3) 722233 (OUS ONLY).

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

FDA Devices Moderate Feb 26, 2025

Brand Name: RayStation- Intended as a Radiation Therapy Treatment Planning System Model/Catalog Number: 13.0.0.1547, 13.1.0.144, 13.1.1.89 and 14.0.…

RAYSEARCH LABORATORIES AB

FDA Devices Moderate Feb 26, 2025

Dexcom G6, Continuous Glucose Monitoring System, REF: STK-OE-001

Dexcom, Inc.

FDA Devices Moderate Feb 26, 2025

Hot Dog PATIENT WARMING, Underbody Warming Mattress + Return Electrode, 89 cm (35"), REF US530, to prevent or treat hypothermia

Augustine Temperature Management, LLC

FDA Devices Moderate Feb 26, 2025

LIFEPAK 15 V4/Masimo Rainbow Sensors: Masimo¿ RD rainbow Adt 8¿ SpCO, SpO2, and SpMet, Adult Adhesive Sensors REF 11996-000515 Masimo¿ LNCS-II …

Physio-Control, Inc.

FDA Devices Critical Feb 26, 2025

Allura Xper FD20/10; Catalog numbers: 722029

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

FDA Devices Moderate Feb 26, 2025

Augustine Surgical Inc. HotDog Return Electrode accessory connector cables, Model A136 used in conjunction with Warming Blankets and Mattresses.

Augustine Temperature Management, LLC

FDA Devices Critical Feb 26, 2025

Allura Xper FD10 - Catalog numbers: (1) 722003, (2) 722010, (3) 722026,

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

FDA Devices Moderate Feb 26, 2025

remel BLOOD AGAR MacCONKEY AGAR BIPLATE, REF R02049, QTY 100, for invitro diagnostic use

Remel, Inc

FDA Devices Critical Feb 26, 2025

Allura Xper FD10C; Catalog number: 722001

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

FDA Devices Critical Feb 26, 2025

Cardio Vascular-Allura Centron; Catalog number: 722400 (OUS ONLY).

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

FDA Devices Moderate Feb 26, 2025

Brand Name: RayStation- Intended as a Radiation Therapy Treatment Planning System Model/Catalog Number: 5.0.2.35 and 5.0.3.17 Software Version: Ray…

RAYSEARCH LABORATORIES AB

FDA Devices Critical Feb 26, 2025

Allura Xper FD20/20; Catalog numbers: 722038

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

FDA Devices Moderate Feb 26, 2025

Brand Name: RayStation- Intended as a Radiation Therapy Treatment Planning System Model/Catalog Number: 6.0.0.24 Software Version: RayStation 6

RAYSEARCH LABORATORIES AB

FDA Devices Critical Feb 26, 2025

Azurion 5 M20; Catalog numbers: (1) 722228, (2) 722232 (OUS ONLY), (3) 722281 (OUS ONLY).

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

FDA Devices Moderate Feb 26, 2025

Medline Convenience Kits for Various Procedures: 1) CLOVIS RESP/INTUB DRAWER 2, Model Number ACC010809; 2) RESP/INTUBATION DRAWER #2, Model Number …

MEDLINE INDUSTRIES, LP - Northfield

FDA Devices Critical Feb 26, 2025

Allura Xper FD10/10; Catalog numbers: (1) 722005, (2) 722011, (3) 722027.

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

NHTSA Critical Feb 24, 2025

MERCEDES-BENZ 2021-2023: SERVICE BRAKES, HYDRAULIC:FOUNDATION COMPONENTS

MERCEDES-BENZ

NHTSA Critical Feb 24, 2025

KIA 2025: ELECTRICAL SYSTEM:PROPULSION SYSTEM

KIA

NHTSA Critical Feb 21, 2025

BMW 2025: ELECTRICAL SYSTEM:12V/24V/48V BATTERY:CABLES

BMW

CPSC Moderate Feb 20, 2025

DR Power Equipment Recalls Tow Behind Field & Brush Mowers Due to Laceration Hazard

DR Power Equipment, of South Burlington, Vermont, a subsidiary of Generac Power Systems Inc., of Waukesha, Wisconsin

CPSC Moderate Feb 20, 2025

Fjorden iPhone Camera Grips Recalled Due to Battery Ingestion Hazard; Violation of Reese's Law Federal Safety Regulations for Consumer Products with …

Fjorden Electra AS, of Norway

CPSC Moderate Feb 20, 2025

Holosun Technologies Recalls Two Firearm Dot Sights Due to Battery Ingestion Hazard; Violations of Reese's Law Federal Safety Regulations for Consume…

CPSC Moderate Feb 20, 2025

Homebox Blackout Roller Window Shades Recalled Due to Strangulation and Entanglement Hazards and Risk of Serious Injury or Death; Violation of Federa…

Zhejiang Mingjing Textile Co. Ltd, of China

CPSC Moderate Feb 20, 2025

Kubota Recalls Utility Tractors Due to Crash Hazard

Kubota Tractor Corporation, of Grapevine, Texas

Nearby Recall Years

Browse recalls from adjacent calendar years to see how federal enforcement volume has shifted over time.

Compare 2025 with 2024 →

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 2025

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 2025 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.