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 353 of 782

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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 2 critical (Class I-equivalent) actions, 48 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 18, 2019 to Dec 25, 2019, covering 26 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 25, 2019

Alliance Tech Medical, Inc. All Flow Pulmonary Function Filters, 100 filters individually packaged in a clear, sealed bag printed with the part numbe…

Alliance Tech Medical, Inc

Moderate Dec 25, 2019

Medtronic Affinity, 38um Arterial Filter, Catalog number REF 351

Medtronic Perfusion Systems

Moderate Dec 25, 2019

MICRO-PSD EXTERNAL BEAM PHOTON, Catalog Number: PSD-PE5N - Product Usage: pre-calibrated PSD sensors are intended for use during cancer treatments to…

Angiodynamics, Inc.

Moderate Dec 25, 2019

Arrow EZ-IO Intraosseous Vascular Access System 15mm Needle+Stabilizer Kit, Product Code 9018P-VC-005 - Product Usage: The Arrow EZ-IO Intraosseous V…

Teleflex Medical

Moderate Dec 25, 2019

Elasto-Gel Absorbent Wound Dressing, Item DR8000. 5 Dressings 4" x 4". Sterile. UPC 45713-58000 Bacteriostatic

Southwest Technologies Inc

Moderate Dec 25, 2019

Anesthesia Pediatric Circuit 72", Model DYNJAPF6057A

Medline Industries Inc

Moderate Dec 25, 2019

Walgreens At-Home A1C Test Kit, Software Version Revision D, REF Number 3056

Polymer Technology Systems

Moderate Dec 18, 2019

C7000 - CUSA¿ Clarity Ultrasonic Tissue Ablation System

Integra LifeSciences Corp.

Moderate Dec 18, 2019

C7000 - CUSA¿ Clarity Ultrasonic Tissue Ablation System

Integra LifeSciences Corp.

Moderate Dec 18, 2019

Maquet Cardiopulmonary (MCP)/Getinge ROTAFLOW Drive, Model Number 701022161. The device is a component of the ROTAFLOW System Console.

Maquet Cardiovascular Us Sales, Llc

Moderate Dec 18, 2019

Healix Knotless ADV BR 4.75 Suture Anchor

DePuy Mitek, Inc., a Johnson & Johnson Co.

Moderate Dec 18, 2019

C7000 - CUSA¿ Clarity Ultrasonic Tissue Ablation System

Integra LifeSciences Corp.

Moderate Dec 18, 2019

C7000 - CUSA¿ Clarity Ultrasonic Tissue Ablation System

Integra LifeSciences Corp.

Moderate Dec 18, 2019

Radiofrequency Grounding Pad, REF RF-DGP-L

Abbott Medical

Moderate Dec 18, 2019

C7000 - CUSA¿ Clarity Ultrasonic Tissue Ablation System

Integra LifeSciences Corp.

Moderate Dec 18, 2019

Maquet Cardiopulmonary GmbH / Getinge Quadrox-iD Pediatric Diffusion Membrane Oxygenator with Bioline Coating, Sterile REF: BEQ-HMOD 30000

GETINGE US SALES LLC

Moderate Dec 18, 2019

Biopsy Needle FPU Kit, Product # 9731754, UDI: 00643169341517

Medtronic Navigation, Inc.

Moderate Dec 18, 2019

Ligamax 5 mm Endoscopic Multiple Clip Applier

Ethicon Endo-Surgery Inc

Moderate Dec 18, 2019

C7000 - CUSA¿ Clarity Ultrasonic Tissue Ablation System

Integra LifeSciences Corp.

Moderate Dec 18, 2019

Coated PGA Undyed Polyglycolic Acid Braided Absorbable Suture Sterile EO 18" (45cm); UDI: (01)10790986000657 (17)220430 (10)17050970

CP Medical Inc

Moderate Dec 18, 2019

C7000 - CUSA¿ Clarity Ultrasonic Tissue Ablation System

Integra LifeSciences Corp.

Moderate Dec 18, 2019

C7000 - CUSA¿ Clarity Ultrasonic Tissue Ablation System

Integra LifeSciences Corp.

Moderate Dec 18, 2019

C7000 - CUSA¿ Clarity Ultrasonic Tissue Ablation System

Integra LifeSciences Corp.

Moderate Dec 18, 2019

C7000 - CUSA¿ Clarity Ultrasonic Tissue Ablation System

Integra LifeSciences Corp.

Moderate Dec 18, 2019

C7000 - CUSA¿ Clarity Ultrasonic Tissue Ablation System

Integra LifeSciences Corp.

Moderate Dec 18, 2019

C7000 - CUSA¿ Clarity Ultrasonic Tissue Ablation System

Integra LifeSciences Corp.

Critical Dec 18, 2019

CrossCath Support Catheter, RPN CXC3.4-2.2-18-90-P-NS-0, Order Number G51575 For diagnostic and interventional vascular procedures.

Cook Inc.

Critical Dec 18, 2019

CrossCath Support Catheter, RPN CXC3.4-2.2-18-150-P-NS-0, Order Number G51577 For diagnostic and interventional vascular procedures.

Cook Inc.

Moderate Dec 18, 2019

P28, Titan 3-D Wedge, Evans, Large, 10 mm, sterile, REF P03-EVN-1010-S, Type: Lagrge, Size: 10mm, (01) 00889795018182, Sterile R, Single Use Only

Paragon 28, Inc.

Moderate Dec 18, 2019

C7000 - CUSA¿ Clarity Ultrasonic Tissue Ablation System

Integra LifeSciences Corp.

Moderate Dec 18, 2019

Oral-B, Practitioner Series, 5% Sodium Fluoride Varnish, 500 units (40mL/each) - Product Usage: For dentinal hypersensitivity and for the reduction o…

Young Dental Manufacturing Co, LLC

Moderate Dec 18, 2019

Elecsys Anti-HAV IgM assay-for the in vitro qualitative detection of IgM antibodies to hepatitis A virus (anti-HAV IgM) in human serum and plasma C…

Roche Diagnostics Operations, Inc.

Moderate Dec 18, 2019

C7000 - CUSA¿ Clarity Ultrasonic Tissue Ablation System

Integra LifeSciences Corp.

Moderate Dec 18, 2019

C7000 - CUSA¿ Clarity Ultrasonic Tissue Ablation System

Integra LifeSciences Corp.

Moderate Dec 18, 2019

VNS Therapy Program GMDN: 44077 Model # 3000 V1.5.2, RxOnly

LivaNova USA Inc

Moderate Dec 18, 2019

BOND Polymer Refine Detection Kit, Catalog No. DS9800. This detection system is for in vitro diagnostic use. Bond Polymer Refine Detection is a bio…

Leica Microsystems, Inc.

Moderate Dec 18, 2019

C7000 - CUSA¿ Clarity Ultrasonic Tissue Ablation System

Integra LifeSciences Corp.

Moderate Dec 18, 2019

C7000 - CUSA¿ Clarity Ultrasonic Tissue Ablation System

Integra LifeSciences Corp.

Moderate Dec 18, 2019

Cognision, Subject Kit (Clinical Grade), Model 3000- containing Hydro Dot brand Wave Prep cups-electroconductive cream for use with external electrod…

Neuronetrix Solutions, LLC dba Cognision

Moderate Dec 18, 2019

iTotal CR Knee Replacement System Model Number: TCR-111-1111-010102 - Product Usage: The iTotal CR Knee Replacement System is intended for use as a …

Conformis, Inc.

Moderate Dec 18, 2019

C7000 - CUSA¿ Clarity Ultrasonic Tissue Ablation System

Integra LifeSciences Corp.

Moderate Dec 18, 2019

C7000 - CUSA¿ Clarity Ultrasonic Tissue Ablation System

Integra LifeSciences Corp.

Moderate Dec 18, 2019

Optilite C-Reactive Protein Kit - Product Usage: The Optilite C-Reactive Protein Reagent is intended for the quantitative in vitro determination of C…

The Binding Site Group, Ltd.

Moderate Dec 18, 2019

C7000 - CUSA¿ Clarity Ultrasonic Tissue Ablation System

Integra LifeSciences Corp.

Moderate Dec 18, 2019

C7000 - CUSA¿ Clarity Ultrasonic Tissue Ablation System

Integra LifeSciences Corp.

Moderate Dec 18, 2019

C7000 - CUSA¿ Clarity Ultrasonic Tissue Ablation System

Integra LifeSciences Corp.

Moderate Dec 18, 2019

C7000 - CUSA¿ Clarity Ultrasonic Tissue Ablation System

Integra LifeSciences Corp.

Moderate Dec 18, 2019

Habib EUS RFA, 10mm electrode active tip, Material Number/UPN: 6500 - Product Usage: The Habib EUS RFA is indicated for coagulation and ablation of s…

Boston Scientific Corporation

Moderate Dec 18, 2019

C7000 - CUSA¿ Clarity Ultrasonic Tissue Ablation System

Integra LifeSciences Corp.

Moderate Dec 18, 2019

SKINFUSE Resuce Calming Complex Kit containing: SKINFUSE LIFT HG - Product Usage: The SKINFUSE Rescue Calming Complex is intend to be used to soothe…

Bellus Medical

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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.