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 28 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 1 critical (Class I-equivalent) actions, 47 moderate recalls, and 2 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 17, 2025, covering 10 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).

Low Dec 17, 2025

Brand Name: Pillar" SA PTC Spacer System Product Name: Pillar" SA PTC Spacer System Model/Catalog Number: 39-9012SP 33W X 28L X 12.5H, 7DEG PTC IMP…

Orthofix U.S. LLC

Low Dec 17, 2025

Brand Name: FORZA" PTC Spacer System Product Name: FORZA" PTC Spacer System Model/Catalog Number: 38-1007SP FORZA PTC Spacer, Straight, 0¿, 9W x 23…

Orthofix U.S. LLC

Moderate Dec 17, 2025

BD InLay Optima Ureteral Stent Kit Size: 8 Fr. x 26 cm, Ureteral Stent Kit REF 78826

C.R. Bard Inc

Moderate Dec 10, 2025

IntelliVue MP90. Product Number: M8010A.

Philips North America Llc

Moderate Dec 10, 2025

Food Intolerance Test Small

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Moderate Dec 10, 2025

IntelliVue MP30. Product Number: M8002A.

Philips North America Llc

Moderate Dec 10, 2025

Vitamin D-Test

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Moderate Dec 10, 2025

Candida Test

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Moderate Dec 10, 2025

Organic Acids Profile Test Large

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Moderate Dec 10, 2025

Allergy Test IgE

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Moderate Dec 10, 2025

Allergy test Small

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Moderate Dec 10, 2025

IntelliVue Patient Monitor MX800. Product Number: 865240.

Philips North America Llc

Moderate Dec 10, 2025

GI Microbiome Profile XL

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Moderate Dec 10, 2025

Illegally Marketed

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Moderate Dec 10, 2025

HPV Antigen Test

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Moderate Dec 10, 2025

Lumify Diagnostic Ultrasound System models : 795005, 795161, 989605449841,

Philips Ultrasound, LLC

Moderate Dec 10, 2025

Sperm Test

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Moderate Dec 10, 2025

Mycoplasma test, IgG and IgM

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Moderate Dec 10, 2025

Parasite Test

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Moderate Dec 10, 2025

Adrenal Test

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Moderate Dec 10, 2025

Neurotransmitters Plus

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Moderate Dec 10, 2025

Welch Allyn INF BAG, Thigh 1-Tube, Model/Catalog Number: REF 5089-18; Product replacement bladder for the Welch Allyn Two-Piece Blood Pressure Cuff.

Baxter Healthcare Corporation

Moderate Dec 10, 2025

Pollen Allergy Test

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Moderate Dec 10, 2025

Ivenix Infusion System (IIS), Large Volume Pump. Model Number: LVP-0004.

Fresenius Kabi USA, LLC

Moderate Dec 10, 2025

Alcohol (ALC) Test Saliva

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Moderate Dec 10, 2025

Gut Microbiome Test XL

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Moderate Dec 10, 2025

Pet Allergy Test

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Moderate Dec 10, 2025

IntelliVue Patient Monitor MX700. Product Number: 865241.

Philips North America Llc

Moderate Dec 10, 2025

CT 5300; Software Version Number: 4.5, 5.0, 5.1;

Philips North America Llc

Moderate Dec 10, 2025

Urinary Tract Infection Test

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Moderate Dec 10, 2025

IntelliVue Patient Monitor MX500. Product Number: 866064.

Philips North America Llc

Moderate Dec 10, 2025

Lactose Intolerance Test

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Moderate Dec 10, 2025

Phantom Fibula Nail, 2.8mm x 130mm, Right, Ti, Fibula Nail, REF: P36-128-130R-S

Paragon 28, Inc.

Moderate Dec 10, 2025

PSA Test

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Moderate Dec 10, 2025

IntelliVue Patient Monitor MX850. Product Number: 866470.

Philips North America Llc

Moderate Dec 10, 2025

Gut Microbiome Test Small

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Moderate Dec 10, 2025

8 in 1 STI Test Kit

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Moderate Dec 10, 2025

Akkermansia Test

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Moderate Dec 10, 2025

MAMMOMAT Inspiration;

Siemens Medical Solutions USA, Inc

Moderate Dec 10, 2025

Food Intolerance Test Medium

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Moderate Dec 10, 2025

KWIK-STIK, Quality control kit for culture media, Vibrio parahaemolyticus derived from ATCC 17802, Catalog Number 0818K

Microbiologics Inc

Moderate Dec 10, 2025

MAMMOMAT Fusion;

Siemens Medical Solutions USA, Inc

Moderate Dec 10, 2025

IntelliVue MP2. Product Number: M8102A.

Philips North America Llc

Moderate Dec 10, 2025

Food Sensitivity Test Large

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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

Moderate Dec 10, 2025

Mycotoxin Panel Test

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Moderate Dec 10, 2025

Food Sensitivity Test Small

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Moderate Dec 10, 2025

Allergy test Small

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Moderate Dec 10, 2025

Peptic Ulcer Test (H, pylori)

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Moderate Dec 10, 2025

Heavy Metals 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.