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 405 of 782
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 18 critical (Class I-equivalent) actions, 29 moderate recalls, and 3 lower-severity notices. Approximately 50 of 50 entries name a specific recalling firm, while 49 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 6, 2019 to Feb 20, 2019, 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).
Stationary Fluoroscopic X-ray System CombiDiagnost R90, Model 709030 Stationary Fluoroscopic X-ray System
Philips Medical Systems Gmbh, DMC
COBRA FUSION 50, Ablation System, Catalog # (REF) 700-002
AtriCure, Inc.
21Y14=S PushValve upper part Product Usage: The PushValves/ MagValves is intended exclusively for the prosthetic fitting of lower limb amputees. …
Ottobock Orthopedic Industrie
Medtronic implantable pulse generator: SENSIA, Dual chamber pacemaker (DDD): (a) Model Number SED01 (b) Model Number SEDR01 (c) Model Number SED…
Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
Vergene Amplification Tray - 700uL, BC-GP REF 20-011-018 The Verigene(R) Gram-Positive Blood Culture Nucleic Acid Test (BC-GP) performed using the…
Luminex Corporation
HORIZON Ez Arm (Part of the HORIZON TMS Therapy System.)
The Magstim Company Limited
Genius Knee Cemented CR Femoral Component Product Usage: Knee replacement component
Signature Orthopedics Pty Limited
ATLAS Loading Car
Steris Corporation
Edward Lifesciences, Edwards Commander Delivery System: Model Number UDI Number 9600LDS20A (US) 00690103193930 9600LDS20J 00690103194852 9600LDS2…
Edwards Lifesciences, LLC
Medtronic implantable pulse generator: Versa, Dual chamber rate responsive pacemaker (DDDR), Model Number VEDR01
Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
Medtronic implantable pulse generator: ADAPTA, Dual chamber pacemaker (DDD): (a) Model Number ADD01 (b) Model Number ADDR01 (c) Model Number ADD…
Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
Medtronic implantable pulse generator: Sphera DR MRI SureScan, Dual chamber rate responsive pacemaker (DDDR): (a) Model Number SPDR01 (b) Model N…
Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
Aguja de Aspiracion con Profundidad Ajustable Tipo I 16ga x 5 cm- Product Usage: Manual surgical instruments for Bone Marrow Biopsy and Aspiration.
Angiotech (Manan Medical Products, Inc.)
GE Healthcare Centricity Universal Viewer Breast Imaging Centricity Universal Viewer is a device that displays medical images and data from var…
GE Healthcare, LLC
Portex 5ml Normal Saline (0.9%) Unit Dose¿¿¿¿ ¿
Medex Cardio-Pulmonary Inc., d.b.a. Smiths Medical Company
Portex 550 ml Sterile Water Humidifier w/5psi Adapt.¿¿¿¿ ¿¿¿¿ ¿¿¿ ¿¿¿
Medex Cardio-Pulmonary Inc., d.b.a. Smiths Medical Company
Aguja para Biopsia Tipo Medula Osea Ergonomica 11ga x 10cm
Angiotech (Manan Medical Products, Inc.)
Medline Prefilled 350 ml Sterile¿¿¿¿ ¿¿¿¿ ¿
Medex Cardio-Pulmonary Inc., d.b.a. Smiths Medical Company
Ascension Modular Radial Head (MRH) Radial Head Implant, Catalog Number, MRH-350-04-WW
Ascension Orthopedics, Inc
ARCHITECT Free T3 Reagent Kit used on ARCHITECT i1000SR or i2000/i2000SR platforms Product Usage: It is a Chemiluminescent Microparticle Immunoas…
Abbott Ireland Diagnostics Division
Richard Wolf Bronchoscope Tubes, Model Texas. Device is reusable and should be sterilized prior to each use. Product Usage: Bronchoscopes are intend…
Richard Wolf GmbH
Intermed 350 ml Sterile Water Humidifier w/5psi Adapt.¿¿¿¿ ¿¿¿ ¿¿¿
Medex Cardio-Pulmonary Inc., d.b.a. Smiths Medical Company
Medline 300-350 ml Sterile Water Humidifier w/5psi Adapt.¿¿¿¿ ¿
Medex Cardio-Pulmonary Inc., d.b.a. Smiths Medical Company
NeuViz 128 Multi-slice CT Scanner System with software version 1.0.8.5010O+P04 Vi .0.8.521 9+PO1 Multi-Slice CT Scanner System can be used as a who…
NEUSOFT MEDICAL SYSTEMS IMP & EX
CoaguChek XS PT Test; All Catalog/REF Numbers that do NOT end in 160 The CoaguChek XS PT test strips are part of the CoaguChek XS System. The Coag…
TERRIFIC CARE LLC
Portex Unit Dose 5 ml Normal Saline (0.9%)¿¿¿¿ ¿
Medex Cardio-Pulmonary Inc., d.b.a. Smiths Medical Company
J Type Bone Marrow Needle 13ga x 6cm - Product Usage: Manual surgical instruments for Bone Marrow Biopsy and Aspiration.
Angiotech (Manan Medical Products, Inc.)
Aguja de Aspiration con Profundidad Ajustable Tipo I 15ga x 5 cm - Product Usage: Manual surgical instruments for Bone Marrow Biopsy and Aspiratio…
Angiotech (Manan Medical Products, Inc.)
Portex Unit Dose 15 ml Normal Saline ¿
Medex Cardio-Pulmonary Inc., d.b.a. Smiths Medical Company
BD FACSLyric 3L 10C with FACSuite Clinical Software v1.1.1, catalog number 662878 BD FACSLyric is a high-performance flow cytometer designed to su…
Becton, Dickinson and Company, BD Biosciences
Medline Prefilled 550 ml Sterile¿¿ ¿
Medex Cardio-Pulmonary Inc., d.b.a. Smiths Medical Company
ARCHITECT Total T3 Reagent Kit used on ARCHITECT i1000SR or i2000/i2000SR platforms Product Usage: It is a Chemiluminescent Microparticle Immunoa…
Abbott Ireland Diagnostics Division
Henry Schein CU 1000 Halogen Curing Light, Catalog 900-4542. - Product Usage: Curing light for use in dentistry. The labeling did not provide specifi…
Handpiece Headquarters
MEDTRONIC CARELINK 2090 programmer
Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
Intermed 550 ml Sterile Water Humidifier w/5psi Adapt.¿¿¿¿
Medex Cardio-Pulmonary Inc., d.b.a. Smiths Medical Company
MEDTRONIC CARELINK 29901 Programmer for Medtronic and Vitaron Devices
Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
Product: ABL800 FLEX with Crea. The ABL800 with Crea is available in the following configurations: ABL817, ABL827 and ABL837. ABL800 Series Ref. 3…
Radiometer America Inc
J Type Bone Marrow Needle 13ga x 10 cm- Product Usage: Manual surgical instruments for Bone Marrow Biopsy and Aspiration.
Angiotech (Manan Medical Products, Inc.)
BARD SureStep Foley Tray System Bardex I.C. Complete Care Temperature Sensing Infection Control Foley Catheter with Bard Hydrogel and Bacteria-Guard …
Bard Medical Division
ARJOHUNTLEIGH GETINGE GROUP, RotoProne Therapy System, Model Number 209800
Arjohuntleigh Magog
"J" Type Bone Marrow Needle 11ga x 10 cm - Product Usage: Manual surgical instruments for Bone Marrow Biopsy and Aspiration.
Angiotech (Manan Medical Products, Inc.)
Portex 550 ml Sterile Water Humidifier w/5psi Adapt.¿¿¿¿ ¿¿¿
Medex Cardio-Pulmonary Inc., d.b.a. Smiths Medical Company
Double Diamond J Type Bone Marrow Needle & Marrow Extraction Cannula 11ga x 10cm 14MTWX x 12.5 cm
Angiotech (Manan Medical Products, Inc.)
Naera Hospital Bassinet, Model No. 4402
Stryker Medical Division of Stryker Corporation
Revolution CT systems with the SmartStep Option The system is intended for head, whole body, cardiac and vascular X-ray Computed Tomography applic…
GE Healthcare, LLC
Portex 350 ml Sterile Water Humidifier w/5psi Adapt.¿¿¿¿
Medex Cardio-Pulmonary Inc., d.b.a. Smiths Medical Company
Portex 500 ml Sterile Water USP Pour Bottle¿¿¿¿ ¿¿¿
Medex Cardio-Pulmonary Inc., d.b.a. Smiths Medical Company
SureStep(TM) FOLEY TRAY SYSTEM, Preconnected Closed System Foley Tray, Product Codes: A119214M, A119216M, A119218M, A119416M, A153200, A300916A, A30…
Bard Medical Division
Portex 1000 ml Sterile Water USP Pour Bottle¿¿¿¿ ¿¿¿
Medex Cardio-Pulmonary Inc., d.b.a. Smiths Medical Company
Cell Saver Elite Processing Kit, 70 ml, Product ID: CSE-P-70 Indications for Use: The Haemonetics Cell Saver 5/5+ System and its related accessory…
Haemonetics Corporation
Nearby Agencies
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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.
- Source: FDA Medical Devices - verify with the issuing agency: official recall page →
- Source: PlainRecalls Data Index - aggregated from FDA openFDA, CPSC, and NHTSA public databases
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.