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 529 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 1 critical (Class I-equivalent) actions, 42 moderate recalls, and 7 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 Feb 22, 2017 to Mar 1, 2017, covering 24 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 Mar 1, 2017

Oxford Partial Knee System Left Medial Tibial Trial Tray Size B Product Usage: Instruments for use with the Oxford Uni Partial Knee System

Biomet U.K., Ltd.

Moderate Mar 1, 2017

ETEST XM256 (Cefuroxime), Foam: 506958-506918; SPB: 412304-412305 ETEST is a quantitative technique for determining the antimicrobial susceptibili…

BioMerieux SA

Moderate Mar 1, 2017

Keyspan High-High Speed USB to Serial Adapter Product Usage: The Reporting Software is an application which serves as middle ware between the Tos…

Tosoh Smd Inc

Moderate Mar 1, 2017

Oxford Partial Knee System Left Medial Tibial Trial Tray Size F Product Usage: Instruments for use with the Oxford Uni Partial Knee System

Biomet U.K., Ltd.

Moderate Mar 1, 2017

DIAMONDBACK 360 Peripheral 1.50 Classic, Model DBP-150CLASS145 Peripheral Orbital Atherectomy System (OAS) is a minimally invasive, catheter-based O…

Cardiovascular Systems Inc

Moderate Mar 1, 2017

GrebSet Micro-Introducer Kit, model 7941, Sterilized with Ethylene Oxide. Product Usage: The GrebSet micro-introducer kit is intended to facilit…

Vascular Solutions, Inc.

Low Mar 1, 2017

DeRoyal Heart Tracecart REF 53-1769, Rx Only, NON-STERILE PRODUCT CONTAINED WITHIN.

DeRoyal Industries Inc

Moderate Mar 1, 2017

Smith & Nephew Dyonics Saw Blade, Short, Product Number 3703

Smith & Nephew, Inc.

Moderate Mar 1, 2017

Oxford Partial Knee System Phase 3 Tibial Template Left Medial Size C Product Usage: Instruments for use with the Oxford Uni Partial Knee System

Biomet U.K., Ltd.

Low Mar 1, 2017

AMT 12 inch Right Angle Feeding Set with Y-Port Used with Nasogastric/Nasointestinal (NG/NI) tubes.

Applied Medical Technology Inc

Moderate Mar 1, 2017

Oxford Partial Knee System Left Medial Tibial Trial Tray Size A Product Usage: Instruments for use with the Oxford Uni Partial Knee System

Biomet U.K., Ltd.

Moderate Mar 1, 2017

Oxford Partial Knee System Right Medial Tibial Trial Tray Size C Oxford Partial Knee System Left Medial Tibial Trial Tray Size C

Biomet U.K., Ltd.

Moderate Mar 1, 2017

Merge Eye Station Import Utility (ESIU) when used with Merge Eye Station and Merge Eye Care PACS. The firm name on the labeling is Merge Healthcare,…

Merge Healthcare, Inc.

Moderate Mar 1, 2017

Smith & Nephew Dyonics Saw Blade, Long, Special, Product Number 3706

Smith & Nephew, Inc.

Moderate Mar 1, 2017

Oxford Unicompartmental Knee Phase 3 Shim Size 3 Product Usage: Instruments for use with the Oxford Uni Partial Knee System

Biomet U.K., Ltd.

Moderate Mar 1, 2017

Oxford Unicompartmental Knee Phase 3 Shim Size 1 Product Usage: Instruments for use with the Oxford Uni Partial Knee System

Biomet U.K., Ltd.

Moderate Mar 1, 2017

Oxford Unicompartmental Knee Phase 3 Tibial Impactor Product Usage: Instruments for use with the Oxford Uni Partial Knee System

Biomet U.K., Ltd.

Moderate Mar 1, 2017

Durex Pleasure Pack . 3 ultra fine lubricated latex condoms 12 ultra fine lubricated latex condoms 24 Ra fine lubricated latex condoms 3 …

Reckitt Benckiser LLC

Moderate Mar 1, 2017

Smith & Nephew Dyonics Saw Blade, Standard, Thick, Product Number 3702

Smith & Nephew, Inc.

Moderate Mar 1, 2017

Oxford Partial Knee System Phase 3 Tibial Template Right Medial Size C Product Usage: Instruments for use with the Oxford Uni Partial Knee System

Biomet U.K., Ltd.

Moderate Mar 1, 2017

Oxford Partial Knee System Phase 3 Tibial Template Left Medial Size B Product Usage: Instruments for use with the Oxford Uni Partial Knee System

Biomet U.K., Ltd.

Moderate Mar 1, 2017

Oxford Partial Knee System Left Medial Tibial Trial Tray Size D Product Usage: Instruments for use with the Oxford Uni Partial Knee System

Biomet U.K., Ltd.

Moderate Mar 1, 2017

Oxford Partial Knee System Right Medial Tibial Trial Tray Size A Product Usage: Instruments for use with the Oxford Uni Partial Knee System

Biomet U.K., Ltd.

Moderate Mar 1, 2017

Jackson-Pratt Channel Drain Silicone Round, Fully Fluted w/10FR Trocar. Sterile. Rx Distributed by Cardinal Health, USA Catalog Number: JP-2187…

Degania Silicone, Ltd.

Moderate Mar 1, 2017

Oxford Partial Knee System Right Medial Tibial Trial Tray Size B Product Usage: Instruments for use with the Oxford Uni Partial Knee System

Biomet U.K., Ltd.

Low Mar 1, 2017

Daavlin Aquex (DAAV1000)

Hidrex GmbH

Moderate Mar 1, 2017

Oxford Partial Knee System Phase 3 Tibial Template Right Medial Size A Product Usage: Instruments for use with the Oxford Uni Partial Knee System

Biomet U.K., Ltd.

Low Mar 1, 2017

SRHS DeRoyal Heart Tracecart REF 53-1913, Rx Only, NON-STERILE PRODUCT CONTAINED WITHIN.

DeRoyal Industries Inc

Moderate Mar 1, 2017

Tosoh Bioscience HLC-723G8 Analyzer for HbA1c testing.

Tosoh Bioscience, Inc.

Moderate Mar 1, 2017

Titan" Stabilizer Attachment and Titan TM 360 Stabilizer Attachment

Terumo Cardiovascular Systems Corporation

Moderate Mar 1, 2017

Oxford Partial Knee System Right Medial Tibial Trial Tray Size D Product Usage: Instruments for use with the Oxford Uni Partial Knee System

Biomet U.K., Ltd.

Moderate Mar 1, 2017

Oxford Knee System Tibial Resector Body Tube & Guides Product Usage: Instruments for use with the Oxford Uni Partial Knee System

Biomet U.K., Ltd.

Moderate Mar 1, 2017

Influenza Transport Swab Packages, Reference #20171, One lot with 1010 packages (each package contains 25 transport tubes). The Influenza Swabs i…

Quidel Corporation

Low Mar 1, 2017

AMT Bridle - Nasal Tube Retaining System Used with Nasogastric/Nasointestinal (NG/NI) tubes.

Applied Medical Technology Inc

Moderate Mar 1, 2017

The Sarns Centrifugal Pump is a single use device sterilized by ethylene oxide gas. The device is sold single sterile in cartons of 8 units, or m…

Terumo Cardiovascular Systems Corporation

Moderate Mar 1, 2017

Vascular catheter introduction kit The PICC is indicated for short or long term peripheral access to the central Venous system for intravenous thera…

Arrow International Inc

Moderate Mar 1, 2017

Oxford Unicompartmental Knee Phase 3 Shim Size 2 Product Usage: Instruments for use with the Oxford Uni Partial Knee System

Biomet U.K., Ltd.

Low Mar 1, 2017

Hidrex USA DVP1000

Hidrex GmbH

Low Mar 1, 2017

Hidrex USA DP450

Hidrex GmbH

Moderate Mar 1, 2017

N Latex HCY REAGENT, REF/Catalog OPAX03 /SMN 10445973 , IVD Product Usage: In-vitro diagnostic reagents for the quantitative determination of t…

Siemens Healthcare Diagnostics, Inc.

Moderate Feb 22, 2017

Maquet Express Dry Seal Suction OCEAN DRAIN, SINGLE Reference: 2002-400 Intended Use: To evacuate air and/or fluid from the chest cavity or medias…

Atrium Medical Corporation

Moderate Feb 22, 2017

Atrium PVC 8 Fr Straight Thoracic Catheter Code Number: 8008

Atrium Medical Corporation

Moderate Feb 22, 2017

STERRAD NX Sterilization System, Product Code: 10033, 10033-002

Advanced Sterilization Products

Moderate Feb 22, 2017

StarClose SE Vascular Closure System, Part No. 14679-01, 14679-02. The UDI is 08717648079467. The GMDN is 47411.

Abbott Vascular

Moderate Feb 22, 2017

Vanguard Total Knee, PUNCH THRU TRL PLATES, 63 MM Item No: 32-487261, 67 MM Item No: 32-487262, 71 MM Item No: 32-487263, 75 MM Item No: 32-487264, a…

Zimmer Biomet, Inc.

Moderate Feb 22, 2017

ONCOR Avant-garde, medical charged-particle radiation therapy system Product Usage: The intended use of the SIEMENS branded PRIMUS family of lin…

Siemens Medical Solutions USA, Inc

Moderate Feb 22, 2017

HARVEST NEEDLE 15GA X 2 Intended for the purpose of harvesting bone and/or bone marrow specimens

Argon Medical Devices, Inc

Moderate Feb 22, 2017

Maquet Ocean Water Seal Chest Drain, Single Collection w/AC Reference: 2002-100 Intended Use: To evacuate air and/or fluid from the chest cavity …

Atrium Medical Corporation

Moderate Feb 22, 2017

GN200 Caiman HF generators, electrosurgical, cutting & coagulation & accessories

Aesculap Implant Systems LLC

Critical Feb 22, 2017

Comprehensive Reverse Shoulder System Humeral Tray Model 115340

Zimmer Biomet, Inc.

Nearby Agencies

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

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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.

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.