PlainRecalls

2025 Recalls

Compiled from official public sources by the editorial team.

6,168 recalls · Page 9 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 1 critical, 49 moderate, and 0 lower-severity recalls. The page references 6 distinct recalling firms operating in 1 distinct product categories, with 50 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Devices (50), 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 Critical Dec 10, 2025

IVENIX INFUSION SYSTEM, LVP Primary Administration Set, Dual-Inlet, Low-Sorbing, Needle-Free Port, Dual Y-Site (Qty 25). Large Volume Infusion Pump A…

Fresenius Kabi USA, LLC

FDA Devices Moderate Dec 10, 2025

Mycotoxin Panel Test

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FDA Devices Moderate Dec 10, 2025

Food Sensitivity Test Small

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FDA Devices Moderate Dec 10, 2025

Allergy test Small

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FDA Devices Moderate Dec 10, 2025

Peptic Ulcer Test (H, pylori)

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FDA Devices Moderate Dec 10, 2025

Heavy Metals Test

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FDA Devices Moderate Dec 10, 2025

Incisive CT; Software Version Number: 4.5, 5.0, 5.1;

Philips North America Llc

FDA Devices Moderate Dec 10, 2025

Fructose Intolerance Test

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FDA Devices Moderate Dec 10, 2025

Trichomonas Vaginalis test

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FDA Devices Moderate Dec 10, 2025

IntelliVue MP50. Product Number: M8004A.

Philips North America Llc

FDA Devices Moderate Dec 10, 2025

SIBO Test

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FDA Devices Moderate Dec 10, 2025

IntelliVue MP80. Product Number: M8008A.

Philips North America Llc

FDA Devices Moderate Dec 10, 2025

IntelliVue Patient Monitor MX100. Product Number: 867033.

Philips North America Llc

FDA Devices Moderate Dec 10, 2025

Intestinal Worms Test

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FDA Devices Moderate Dec 10, 2025

D-Dimer Test

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FDA Devices Moderate Dec 10, 2025

IntelliVue MP40. Product Number: M8003A.

Philips North America Llc

FDA Devices Moderate Dec 10, 2025

Diabetes HbA1c Test

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FDA Devices Moderate Dec 10, 2025

Olympus OER-Elite

Aizu Olympus Co., Ltd.

FDA Devices Moderate Dec 10, 2025

Candida Test

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FDA Devices Moderate Dec 10, 2025

Syphilis Test

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FDA Devices Moderate Dec 10, 2025

Iodine Test

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FDA Devices Moderate Dec 10, 2025

MPOX Test

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FDA Devices Moderate Dec 10, 2025

Aurora EV-ICD and Clinical EV-ICD, single chamber, extravascular implantable cardioverter defibrillators (ICD), Product Number DVEA3E4

Medtronic, Inc.

FDA Devices Moderate Dec 10, 2025

GI Microbiome Profile Small

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FDA Devices Moderate Dec 10, 2025

Parasite Test

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FDA Devices Moderate Dec 10, 2025

Sperm Test

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FDA Devices Moderate Dec 10, 2025

DHEA Test

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FDA Devices Moderate Dec 10, 2025

Serotonin Test

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FDA Devices Moderate Dec 10, 2025

Female Fertility Test

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FDA Devices Moderate Dec 10, 2025

Gut Microbiome Test Mega

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FDA Devices Moderate Dec 10, 2025

IntelliVue Multi Measurement Server X2. Product Number: M3002A.

Philips North America Llc

FDA Devices Moderate Dec 10, 2025

Food Allergy Panel Test (IgE)

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FDA Devices Moderate Dec 10, 2025

Food Intolerance Test Large

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FDA Devices Moderate Dec 10, 2025

NAD Profile Test

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FDA Devices Moderate Dec 10, 2025

Vitamin D2 and D3 Test

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FDA Devices Moderate Dec 10, 2025

InSure ONE Fecal Immunochemical Test. Labeled as follows: 1. Insure ONE POL Patient Kit - 10 pack. Model Number: 90010. 2. Insure ONE POL Patie…

Enterix, Inc.

FDA Devices Moderate Dec 10, 2025

Leaky Gut Test

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FDA Devices Moderate Dec 10, 2025

Kidney Test

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FDA Devices Moderate Dec 10, 2025

2 in 1 Trichomonas / Gardnerella Test

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FDA Devices Moderate Dec 10, 2025

Menopause (FSH) 2 Tests

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FDA Devices Moderate Dec 10, 2025

Blood Type Test

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FDA Devices Moderate Dec 10, 2025

3 in 1 STI Test

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FDA Devices Moderate Dec 10, 2025

IntelliVue MP60. Product Number: M8005A.

Philips North America Llc

FDA Devices Moderate Dec 10, 2025

Biological Age & Longevity Test

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FDA Devices Moderate Dec 10, 2025

Lyme Test

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FDA Devices Moderate Dec 10, 2025

Drug Test Small (4 substances)

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FDA Devices Moderate Dec 10, 2025

IntelliVue MP5. Product Number: M8105A.

Philips North America Llc

FDA Devices Moderate Dec 10, 2025

Organic acids Test

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FDA Devices Moderate Dec 10, 2025

IntelliVue MP20. Product Number: M8001A.

Philips North America Llc

FDA Devices Moderate Dec 10, 2025

Hair Mineral Analysis

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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.