2025 Recalls
6,236 federal recalls indexed for 2025 · Page 10 of 125
2025 Recall Year Insight
Federal agencies issued 6,236 product recalls indexed by PlainRecalls in calendar year 2025. That represents about 5.97% of the 104,423 total recalls we track from 1995 through the present, and averages roughly 17.1 recalls per day across the FDA, CPSC, USDA FSIS, 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 125 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 10 distinct recalling firms operating in 2 distinct product categories, with 46 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Devices (46), 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, USDA FSIS, or NHTSA for the system-of-record on any specific recall. PlainRecalls indexes this archive for research and consumer awareness purposes.
Drug Test Small (4 substances)
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IntelliVue MP5. Product Number: M8105A.
Philips North America Llc
Organic acids Test
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IntelliVue MP20. Product Number: M8001A.
Philips North America Llc
Hair Mineral Analysis
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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: 20028870/NextSeq 550Dx HO FC Cart v2.5, 75 Cycles, REF: 20031098; NextSeq 550Dx High Output Reagent Kit v2.5 (300 cycles) IVD, REF: 20028871/NextSeq 550Dx HO FC Cart v2.5, 300 Cycles, REF: 20026365; CN NextSeq 550Dx High Output Reagent Kit v2.5 (75 cycles) IVD, REF: 20064341/CN NEXTSEQ 550Dx HO FLOW CELL V2.5, REF: 20062316; CN NextSeq 550Dx High Outpu
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 System
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
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: USDA FSIS Recalls - calendar-year meat, poultry, and processed egg product recall filings
- Source: CPSC + NHTSA - consumer product and vehicle recall feeds for 2025
Every figure on PlainRecalls is rendered directly from official FDA, CPSC, USDA FSIS and NHTSA recall records; no number is typed in by an editor. Figures cover calendar year 2025 across the FDA, CPSC, USDA FSIS 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 September 2026.