PlainRecalls
2023 data Federal recall API Linked to agency record

FDA Medical Devices

All recall actions attributed to FDA Medical Devices in our federal database. Each record links back to the agency's official notice so you can verify status, remedy, and amendments before acting.

U.S. Food and Drug Administration — Medical device recalls

39,096 recalls · Page 29 of 782

Official website →

FDA Medical Devices Recall Insight

PlainRecalls tracks 39,096 recall actions attributed to the FDA Medical Devices in our federal recall index. Across the full PlainRecalls database of 101,704 records spanning 1995 through the present, FDA Medical Devices accounts for roughly 38.4% of all indexed recalls. The agency's stated scope - U.S. Food and Drug Administration — Medical device recalls - determines what classes of products flow through its recall pipeline and how quickly notices reach consumers. With 782 pages of records at 50 recalls per page, this archive represents one of the longest continuous federal enforcement histories accessible to the public.

Looking at the 50 records on this page alone, the severity distribution skews toward 0 critical (Class I-equivalent) actions, 50 moderate recalls, and 0 lower-severity notices. Approximately 50 of 50 entries name a specific recalling firm, while 50 disclose a unit count, the gap reflects regulatory filing norms where firms disclose lot numbers or distribution channels instead of absolute quantities. This page spans recalls from Dec 10, 2025 to Dec 10, 2025, covering 6 distinct firms. Severity mix is a leading indicator: a page weighted toward critical classifications usually signals an active public-health concern, while lower-severity clusters often represent labeling, undeclared-allergen, or minor design corrections.

Agency-level browsing is useful when a defect pattern crosses categories, for example, a supplier contamination can trigger dozens of downstream recalls that share no obvious product tag but a single issuing agency. Use the pagination below to scan the full archive, or combine this agency filter with category and manufacturer views elsewhere on PlainRecalls to intersect the data. Recall records are sourced directly from FDA Medical Devices's public enforcement feeds and are updated as the agency publishes new notices; the federal record is the authoritative version, and this page aggregates what the agency itself has released. For high-stakes decisions, medical, automotive, or childcare, always click through to the recall detail page and cross-verify the recall number against the agency's current site. Record counts reflect all indexed actions regardless of status (ongoing, terminated, or completed).

Moderate Dec 10, 2025

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

Philips North America Llc

Moderate Dec 10, 2025

Fructose Intolerance Test

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Moderate Dec 10, 2025

Trichomonas Vaginalis test

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Moderate Dec 10, 2025

IntelliVue MP50. Product Number: M8004A.

Philips North America Llc

Moderate Dec 10, 2025

SIBO Test

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Moderate Dec 10, 2025

IntelliVue MP80. Product Number: M8008A.

Philips North America Llc

Moderate Dec 10, 2025

IntelliVue Patient Monitor MX100. Product Number: 867033.

Philips North America Llc

Moderate Dec 10, 2025

Intestinal Worms Test

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Moderate Dec 10, 2025

D-Dimer Test

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Moderate Dec 10, 2025

IntelliVue MP40. Product Number: M8003A.

Philips North America Llc

Moderate Dec 10, 2025

Diabetes HbA1c Test

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Moderate Dec 10, 2025

Olympus OER-Elite

Aizu Olympus Co., Ltd.

Moderate Dec 10, 2025

Candida Test

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Moderate Dec 10, 2025

Syphilis Test

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Moderate Dec 10, 2025

Iodine Test

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Moderate Dec 10, 2025

MPOX Test

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Moderate Dec 10, 2025

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

Medtronic, Inc.

Moderate Dec 10, 2025

GI Microbiome Profile Small

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Moderate Dec 10, 2025

Parasite Test

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Moderate Dec 10, 2025

Sperm Test

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Moderate Dec 10, 2025

DHEA Test

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Moderate Dec 10, 2025

Serotonin Test

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Moderate Dec 10, 2025

Female Fertility Test

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Moderate Dec 10, 2025

Gut Microbiome Test Mega

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Moderate Dec 10, 2025

IntelliVue Multi Measurement Server X2. Product Number: M3002A.

Philips North America Llc

Moderate Dec 10, 2025

Food Allergy Panel Test (IgE)

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Moderate Dec 10, 2025

Food Intolerance Test Large

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Moderate Dec 10, 2025

NAD Profile Test

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Moderate Dec 10, 2025

Vitamin D2 and D3 Test

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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.

Moderate Dec 10, 2025

Leaky Gut Test

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Moderate Dec 10, 2025

Kidney Test

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Moderate Dec 10, 2025

2 in 1 Trichomonas / Gardnerella Test

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Moderate Dec 10, 2025

Menopause (FSH) 2 Tests

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Moderate Dec 10, 2025

Blood Type Test

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Moderate Dec 10, 2025

3 in 1 STI Test

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Moderate Dec 10, 2025

IntelliVue MP60. Product Number: M8005A.

Philips North America Llc

Moderate Dec 10, 2025

Biological Age & Longevity Test

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Moderate Dec 10, 2025

Lyme Test

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Moderate Dec 10, 2025

Drug Test Small (4 substances)

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Moderate Dec 10, 2025

IntelliVue MP5. Product Number: M8105A.

Philips North America Llc

Moderate Dec 10, 2025

Organic acids Test

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Moderate Dec 10, 2025

IntelliVue MP20. Product Number: M8001A.

Philips North America Llc

Moderate Dec 10, 2025

Hair Mineral Analysis

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Moderate Dec 10, 2025

IntelliVue Patient Monitor MX600. Product Number: 865242.

Philips North America Llc

Moderate Dec 10, 2025

Gut Microbiome Test Large

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Moderate Dec 10, 2025

Chlamydia Test

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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.

Moderate Dec 10, 2025

Gonorrhea test

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Moderate Dec 10, 2025

Cholesterol Test

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Nearby Agencies

Explore recalls from other federal agencies that share oversight of product safety.

Compare FDA Medical Devices with FDA Food Safety →

Learn More About Recalls

Disclaimer: This information is provided for informational purposes only and does not constitute professional advice. Consult a qualified professional before making decisions based on this data.

Compiled from official public sources by the editorial team.

Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. Recall counts and figures reflect FDA Medical Devices's own published filings, aggregated alongside the other two 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.