2025 Recalls
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.
IntelliVue Patient Monitor MX600. Product Number: 865242.
Philips North America Llc
Gut Microbiome Test Large
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Chlamydia Test
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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.
Gonorrhea test
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Cholesterol Test
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Iron Deficiency Test (ferritin)
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Thyroid TSH Test
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Herpes (HSV-1 & HSV-2) Test
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Iron Deficiency Test
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Diabetes Test (ketones & glucose)
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Liver Test
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IntelliVue Patient Monitor MX400. Product Number: 866060.
Philips North America Llc
Pregnancy Test
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Allergy & Food Intolerance Test
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Ovulation Test (5 tests)
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IntelliVue Multi-Measurement Module X3. Product Number: 867030.
Philips North America Llc
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.
Food Sensitivity Test Medium
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Olympus OER-Pro
Aizu Olympus Co., Ltd.
Men s Hormone Test
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H pylori (Peptic ulcer) Test
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MAMMOMAT Revelation;
Siemens Medical Solutions USA, Inc
IntelliVue Patient Monitor MX550. Product Number: 866066.
Philips North America Llc
Neurotransmitters Basic
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Epstein-Barr Virus (EBV VCA & EBNA IgG) Test
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Fecal Occult Blood Test
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IntelliVue Patient Monitor MX750. Product Number: 866471.
Philips North America Llc
Women s Hormone Test
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Melatonin Test
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Olympus OER-Mini
Aizu Olympus Co., Ltd.
IntelliVue Patient Monitor MX450. Product Number: 866062.
Philips North America Llc
Neurotransmitters XL
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IBS Test
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Sorbitol Intolerance Test
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Environmental Pollutants Profile Test
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Vaginal PH Test
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Gut Microbiome Test Medium
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Estrogen & Progesterone Test
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IntelliVue MP70. Product Number: M8007A.
Philips North America Llc
Continuous Glucose Monitor (CGM)
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LUCID 2026: SEATS
LUCID
VOLKSWAGEN 2025: AIR BAGS:SENSOR:OCCUPANT CLASSIFICATION:FRONT PASSENGER
VOLKSWAGEN
DODGE 2024: SERVICE BRAKES, HYDRAULIC:PEDALS AND LINKAGES
DODGE
ALFA ROMEO 2024: EXTERIOR LIGHTING:HEADLIGHTS
ALFA ROMEO
INIU Recalls Power Banks Due to Fire and Burn Hazards; Sold on Amazon
Shenzhen Topstar Industry Co., Ltd., of China
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
CreateOn Recalls Pip-Cubes Due to Risk of Serious Injury or Death from Magnet Ingestion Hazard
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
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.
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.