PlainRecalls

2025 Recalls

6,168 recalls · Page 108 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 14 critical, 36 moderate, and 0 lower-severity recalls. The page references 25 distinct recalling firms operating in 5 distinct product categories, with 35 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Devices (31), NHTSA (11), CPSC (8), 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 19, 2025

Microbiologics Multi-Strain Human Papillomavirus (HPV) Verification Panel (Inactivated Pellet), REF 8235; in-vitro diagnostic test

Microbiologics Inc

FDA Devices Moderate Feb 19, 2025

MOSAIQ Oncology Information System

Elekta, Inc.

FDA Devices Moderate Feb 19, 2025

Cardinal Health Presource Kits: 1) UROLOGY ROBOTIC PACK, Catalog Number:SOT4FRUWFA; 2) UROLOGY ROBOTIC PACK, Catalog Number:SOT4FRUWFB; 3) UROLOGY…

Cardinal Health 200, LLC

FDA Devices Moderate Feb 19, 2025

stryker Precision Thin, Catalog Number REF 2296-003-155; Micro Oscillating and Sagittal Blades

Stryker Corporation

FDA Devices Moderate Feb 19, 2025

MicoVention Terumo, LVIS Intraluminal Support Device, REF: 213522-CAS, od, 3.5 mm, TL 22 mm, WL 18 mm, Sterile R, CE0297. The intended purpose of th…

MICROVENTION INC.

FDA Devices Moderate Feb 19, 2025

(1) Pyxis MedStation ES, Catalog No. 323; (2) Pyxis Anesthesia Station (PAS), Catalog No. 327; (3) Pyxis MedStation ES Tower, Catalog No. 352; (4)…

CareFusion 303, Inc.

FDA Devices Critical Feb 19, 2025

Max Mobility/Permobil Smart Drive MX2+ SpeedControl Dial Ref: MX2-3DC use in conjunction with the SmartDrive MX2+ Wheelchair Power Assist component.

Max Mobility LLC

FDA Devices Moderate Feb 19, 2025

Vios Monitoring System Bedside Monitor, Model BSM2050, Software Version Numbers 1.54.20 and 1.56.00

Murata Vios, Inc.

FDA Devices Moderate Feb 19, 2025

Cardinal Health Presource Kits: 1) LARYNGOSCOPY PACK, Catalog Number:SRIET0979N;

Cardinal Health 200, LLC

FDA Devices Moderate Feb 19, 2025

BD Pyxis MedStation 4000 REF: 303. Intended to securely store and dispense medications to a qualified and authorized healthcare provider.

CareFusion 303, Inc.

FDA Devices Moderate Feb 19, 2025

Brand Name: The Guardian System Product Name: The Guardian Model/Catalog Number: Model AMSG3-E Product Description: The Guardian is a cardiac diagnos…

Angel Medical Systems, Inc.

FDA Devices Moderate Feb 19, 2025

Biological, Bio52 HealthFirst Mail In Monitoring System, 52 Tests, Item: 1003600. Biological, Bio12 HealthFirst Mail In Monitoring System, 12 Tests,…

HF Acquisition Co LLC

FDA Devices Moderate Feb 19, 2025

Cardinal Health Presource Kits: 1) KIT,ROBOTIC HYSTERECTOMY, Catalog Number:PB4FRHWFA; 2) KIT,ROBOTIC HYSTERECTOMY, Catalog Number:PB4FRHWFB 3) KI…

Cardinal Health 200, LLC

FDA Devices Moderate Feb 19, 2025

Cardinal Health Presource Kits: 1) KIT, CAROTID ENDARTERECTOMY, Catalog Number:PVV20110B; 2) KIT, CAROTID ENDARTERECTOMY, Catalog Number:PVV20110D …

Cardinal Health 200, LLC

FDA Devices Critical Feb 19, 2025

Vaporizer Sevoflurane, Quik-Fil. Model Number: 6682285. Device is a component of Flow-i C20, Flow-i C30, Flow-i C40, Flow-c, Flow-e. For use during …

Getinge Usa Sales Inc

FDA Devices Moderate Feb 19, 2025

Novation XLE Item Number / Product Description: 140-22-70 NV EHXL NTL LNR G00 22MM 140-28-50 NV EHXLNTRL LNR G0 28MM 140-28-51 NV EHXLNTRL LNR G1…

Exactech, Inc.

FDA Devices Moderate Feb 19, 2025

Cardinal Health Presource Kits: 1) KIT,MAXILLOFACIAL,PRESBYTERIAN, Catalog Number:PWV2MF104; 2) KIT,MAXILLOFACIAL,PRESBYTERIAN, Catalog Number:PWV2…

Cardinal Health 200, LLC

FDA Devices Critical Feb 19, 2025

Max Mobility/Permobil Smart Drive MX2+ SpeedControl Dial Ref: MX2-3DCK use in conjunction with the SmartDrive MX2+ Wheelchair Power Assist component.

Max Mobility LLC

FDA Devices Moderate Feb 19, 2025

The MSOT Acuity Echo is a Class 4 medical laser device. The MSOT Acuity is a mobile assembly of electrically-powered components intended for imaging …

Ithera Medical Gmbh

FDA Devices Moderate Feb 19, 2025

Cardinal Health Presource Kits: 1) CHI STD SPINE OPTION 1, Catalog Number:CHIP99SP11; 2) CHI STD SPINE OPTION 1, Catalog Number:CHIP99SP12 3) CHI STD…

Cardinal Health 200, LLC

FDA Devices Moderate Feb 19, 2025

(1) BD Pyxis MedStation ES, Catalog No. 323; (2) BD Pyxis Anesthesia Station (PAS), Catalog No. 327; (3) BD Pyxis MedStation ES Tower, Catalog No. 35…

CareFusion 303, Inc.

FDA Devices Moderate Feb 19, 2025

stryker Precision Thin, Catalog Number REF 2296-003-108; Micro Oscillating and Sagittal Blades

Stryker Corporation

FDA Devices Moderate Feb 19, 2025

Cardinal Health Presource Kits: 1) CHI STD NEURO CRANI OPT 1, Catalog Number:CHIP99NC12; 2) CHI STD NEURO CRANI OPT 1, Catalog Number:CHIP99NC13 3) C…

Cardinal Health 200, LLC

FDA Devices Moderate Feb 19, 2025

BD Pyxis MedStation Auxiliary 4000 REF: 306. Intended to securely store and dispense medications to a qualified and authorized healthcare provider.

CareFusion 303, Inc.

FDA Devices Moderate Feb 19, 2025

Cardinal Health Presource Kits: 1) KIT,NEURO LAMI,MD ANDERSON, Catalog Number:PN76LMM14; 2) KIT,NEURO LAMI,MD ANDERSON, Catalog Number:PN76LMMD9; …

Cardinal Health 200, LLC

FDA Devices Moderate Feb 19, 2025

Cardinal Health Presource Kits: 1) ACDF PACK, Catalog Number: SNEHBACSCA; 2) ACDF PACK, Catalog Number: SNEHBACSCB

Cardinal Health 200, LLC

FDA Devices Moderate Feb 19, 2025

BD Pyxis MedStation ES (Med ES Main) REF: 323. Intended to securely store and dispense medications to a qualified and authorized healthcare provid…

CareFusion 303, Inc.

FDA Devices Moderate Feb 19, 2025

Cardinal Health Presource Kits: 1) OPHTHALMOLOGY ENDO DCR XTRS PK, Catalog Number:SEY30EYRVA; 2) OPHTHALMOLOGY ENDO DCR XTRS PK, Catalog Number:SEY…

Cardinal Health 200, LLC

FDA Devices Moderate Feb 19, 2025

Brand Name: Sertera Biopsy Device Product Name: Sertera Biopsy Device Model/Catalog Number: Sertera-14 Software Version: N/A Product Description:…

Hologic, Inc

FDA Devices Moderate Feb 19, 2025

Alteon XLE Item Number / Product Description: 140-22-70 NV EHXL NTL LNR G00 22MM 140-28-50 NV EHXLNTRL LNR G0 28MM 140-28-51 NV EHXLNTRL LNR G1…

Exactech, Inc.

FDA Devices Moderate Feb 19, 2025

BD Pyxis MedStation Auxiliary ES REF: 324. Intended to securely store and dispense medications to a qualified and authorized healthcare provider.

CareFusion 303, Inc.

NHTSA Critical Feb 19, 2025

VOLKSWAGEN 2022-2024: BACK OVER PREVENTION:SOFTWARE

VOLKSWAGEN

NHTSA Critical Feb 18, 2025

VOLVO 2023-2025: SERVICE BRAKES, AIR:CONTROLS:PROPORTIONING RELAY VALVE

VOLVO

NHTSA Critical Feb 17, 2025

VOLKSWAGEN 2024-2025: ENGINE

VOLKSWAGEN

NHTSA Critical Feb 17, 2025

KIA 2021-2023: ENGINE AND ENGINE COOLING:ENGINE:HARD PARTS INTERNAL/MECHANICAL

KIA

NHTSA Critical Feb 14, 2025

FORD 2022-2023: STEERING:ELECTRIC POWER ASSIST SYSTEM

FORD

NHTSA Critical Feb 14, 2025

FORD 2022-2024: EXTERIOR LIGHTING:TAIL LIGHTS

FORD

NHTSA Critical Feb 14, 2025

FORD 2022-2024: EXTERIOR LIGHTING:TURN SIGNAL

FORD

NHTSA Critical Feb 14, 2025

FORD,LINCOLN 2020-2021: SEAT BELTS

FORD,LINCOLN

NHTSA Critical Feb 14, 2025

TESLA 2023: STEERING:ELECTRIC POWER ASSIST SYSTEM

TESLA

NHTSA Critical Feb 14, 2025

LINCOLN 2015-2017: VISIBILITY:REARVIEW MIRRORS/DEVICES:EXTERIOR

LINCOLN

CPSC Moderate Feb 13, 2025

6-in-1 Pounding Games Recalled Due to Ingestion Hazard; Violation of Federal Regulations for Magnets; Sold Exclusively on Temu.com by DMITOY

DMITOY, of China

CPSC Moderate Feb 13, 2025

AFTCO Recalls Youth Solitude Jackets with Drawstrings Due to Strangulation Hazard

CPSC Moderate Feb 13, 2025

Igloo Recalls More Than One Million 90 Quart Rolling Coolers Due to Fingertip Amputation and Crushing Hazards

Igloo Products Corp., of Katy, Texas

CPSC Moderate Feb 13, 2025

Rechargeable Portable Lamps with Lithium-Ion Batteries Recalled Due to Fire and Burn Hazards; Imported by BlockBlueLight

CPSC Moderate Feb 13, 2025

Setsmart Recalls LoGest Climbing Ropes Due to Fall Hazard

CPSC Moderate Feb 13, 2025

SHEIN Distribution Corporation Recalls Children's Pajama Sets Due to Burn Hazard; Violation of Federal Flammability Regulations; Sold exclusively at …

SHEIN Distribution Corporation, of Los Angeles, California

CPSC Moderate Feb 13, 2025

Target Recalls Spritz™ Resin Hanukkah Dino Menorahs Due to Fire Hazard

CPSC Moderate Feb 13, 2025

Umarex USA Recalls T4E TR50 Air Pistols Due to Impact Hazard

NHTSA Critical Feb 13, 2025

LAND ROVER 2020: AIR BAGS:KNEE BOLSTER

LAND ROVER

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.