PlainRecalls

2025 Recalls

Compiled from official public sources by the editorial team.

6,168 recalls · Page 10 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 4 critical, 46 moderate, and 0 lower-severity recalls. The page references 13 distinct recalling firms operating in 4 distinct product categories, with 46 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Devices (41), CPSC (5), NHTSA (4), 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 Dec 10, 2025

IntelliVue Patient Monitor MX600. Product Number: 865242.

Philips North America Llc

FDA Devices Moderate Dec 10, 2025

Gut Microbiome Test Large

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FDA Devices Moderate Dec 10, 2025

Chlamydia Test

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FDA Devices Moderate Dec 10, 2025

Reagent Kits/ containing flow cells, components of NextSeq 550Dx Instrument: NextSeq 550Dx High Output Reagent Kit v2.5 (75 cycles) IVD, REF: 200288…

Illumina, Inc.

FDA Devices Moderate Dec 10, 2025

Gonorrhea test

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FDA Devices Moderate Dec 10, 2025

Cholesterol Test

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FDA Devices Moderate Dec 10, 2025

Iron Deficiency Test (ferritin)

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FDA Devices Moderate Dec 10, 2025

Thyroid TSH Test

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FDA Devices Moderate Dec 10, 2025

Herpes (HSV-1 & HSV-2) Test

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FDA Devices Moderate Dec 10, 2025

Iron Deficiency Test

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FDA Devices Moderate Dec 10, 2025

Diabetes Test (ketones & glucose)

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FDA Devices Moderate Dec 10, 2025

Liver Test

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FDA Devices Moderate Dec 10, 2025

IntelliVue Patient Monitor MX400. Product Number: 866060.

Philips North America Llc

FDA Devices Moderate Dec 10, 2025

Pregnancy Test

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FDA Devices Moderate Dec 10, 2025

Allergy & Food Intolerance Test

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FDA Devices Moderate Dec 10, 2025

Ovulation Test (5 tests)

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FDA Devices Moderate Dec 10, 2025

IntelliVue Multi-Measurement Module X3. Product Number: 867030.

Philips North America Llc

FDA Devices Moderate Dec 10, 2025

Hemochron Activated Clotting Time Low-Range Test Cuvette, REF: ACT-LR, to be used with the Hemochron Signature ELITE Whole Blood Microcoagulation Sys…

Accriva Diagnostics, Inc.

FDA Devices Moderate Dec 10, 2025

Food Sensitivity Test Medium

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FDA Devices Moderate Dec 10, 2025

Olympus OER-Pro

Aizu Olympus Co., Ltd.

FDA Devices Moderate Dec 10, 2025

Men s Hormone Test

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FDA Devices Moderate Dec 10, 2025

H pylori (Peptic ulcer) Test

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FDA Devices Moderate Dec 10, 2025

MAMMOMAT Revelation;

Siemens Medical Solutions USA, Inc

FDA Devices Moderate Dec 10, 2025

IntelliVue Patient Monitor MX550. Product Number: 866066.

Philips North America Llc

FDA Devices Moderate Dec 10, 2025

Neurotransmitters Basic

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FDA Devices Moderate Dec 10, 2025

Epstein-Barr Virus (EBV VCA & EBNA IgG) Test

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FDA Devices Moderate Dec 10, 2025

Fecal Occult Blood Test

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FDA Devices Moderate Dec 10, 2025

IntelliVue Patient Monitor MX750. Product Number: 866471.

Philips North America Llc

FDA Devices Moderate Dec 10, 2025

Women s Hormone Test

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FDA Devices Moderate Dec 10, 2025

Melatonin Test

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FDA Devices Moderate Dec 10, 2025

Olympus OER-Mini

Aizu Olympus Co., Ltd.

FDA Devices Moderate Dec 10, 2025

IntelliVue Patient Monitor MX450. Product Number: 866062.

Philips North America Llc

FDA Devices Moderate Dec 10, 2025

Neurotransmitters XL

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FDA Devices Moderate Dec 10, 2025

IBS Test

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FDA Devices Moderate Dec 10, 2025

Sorbitol Intolerance Test

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FDA Devices Moderate Dec 10, 2025

Environmental Pollutants Profile Test

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FDA Devices Moderate Dec 10, 2025

Vaginal PH Test

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FDA Devices Moderate Dec 10, 2025

Gut Microbiome Test Medium

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FDA Devices Moderate Dec 10, 2025

Estrogen & Progesterone Test

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FDA Devices Moderate Dec 10, 2025

IntelliVue MP70. Product Number: M8007A.

Philips North America Llc

FDA Devices Moderate Dec 10, 2025

Continuous Glucose Monitor (CGM)

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NHTSA Critical Dec 10, 2025

LUCID 2026: SEATS

LUCID

NHTSA Critical Dec 10, 2025

VOLKSWAGEN 2025: AIR BAGS:SENSOR:OCCUPANT CLASSIFICATION:FRONT PASSENGER

VOLKSWAGEN

NHTSA Critical Dec 9, 2025

DODGE 2024: SERVICE BRAKES, HYDRAULIC:PEDALS AND LINKAGES

DODGE

NHTSA Critical Dec 9, 2025

ALFA ROMEO 2024: EXTERIOR LIGHTING:HEADLIGHTS

ALFA ROMEO

CPSC Moderate Dec 5, 2025

INIU Recalls Power Banks Due to Fire and Burn Hazards; Sold on Amazon

Shenzhen Topstar Industry Co., Ltd., of China

CPSC Moderate Dec 4, 2025

Casaottima 13-Drawer Dressers Recalled Due to Risk of Serious Injury or Death from Tip-Over and Entrapment Hazards; Violates Mandatory Standard for C…

Changzhou Municipal Sea Metal Products Co. Ltd., of China

CPSC Moderate Dec 4, 2025

CreateOn Recalls Pip-Cubes Due to Risk of Serious Injury or Death from Magnet Ingestion Hazard

CPSC Moderate Dec 4, 2025

Cubimana Building Toy Sets Recalled Due to Risk of Serious Injury or Death from Battery Ingestion; Violates Mandatory Standard for Toys; Sold on Shei…

Shenzhen Excellence Qichuang Technology, dba Vatos Toys, of China

CPSC Moderate Dec 4, 2025

Grizzly Industrial Recalls Heavy-Duty Planers Due to Impact and Laceration Hazards

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 July 2026.