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 250 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 100,165 records spanning 1995 through the present, FDA Medical Devices accounts for roughly 39.0% 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 Oct 27, 2021 to Nov 3, 2021, covering 23 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).
REF/Catalogue Number GSXE0030, GORE CARDIOFORM SEPTAL OCCLUDER 30 mm Diameter, Catheter Working Length 75 cm, Delivery Profile 10 Fr, STERILE EO, Rx …
W L Gore & Associates, Inc.
Advia Chemistry Urinary/Cerebrospinal Fluid Protein (UCFP), SMN 11319151
Siemens Healthcare Diagnostics, Inc.
REF/Catalogue Number GSX0020A, GORE CARDIOFORM SEPTAL OCCLUDER 20 mm Diameter, Catheter Working Length 75 cm, Delivery Profile 10 Fr, STERILE EO, Rx …
W L Gore & Associates, Inc.
REF/Catalogue Number GSXE0025B, GORE CARDIOFORM SEPTAL OCCLUDER 25 mm Diameter, Catheter Working Length 75 cm, Delivery Profile 10 Fr, STERILE EO, Rx…
W L Gore & Associates, Inc.
Cliquid MD version 3.4 software used in conjunction with Analyst MD software on SCIEX Citrine & 4500MD series liquid chromatography-tandem mass spect…
AB SCIEX
ROSA One 3.1 Brain application The device is intended for the spatial positioning and orientation of instruments holders or tool guides to be used…
MEDTECH SAS
Oncentra Brachy users using version 4.0 and above with Applicator Modeling license 170283-00
Elekta, Inc.
REF/Catalogue Number GSXE0030B, GORE CARDIOFORM SEPTAL OCCLUDER 30 mm Diameter, Catheter Working Length 75 cm, Delivery Profile 10 Fr, STERILE EO, Rx…
W L Gore & Associates, Inc.
Atellica CH Urinary/Cerebrospinal Fluid Protein (UCFP), SMN 11097543
Siemens Healthcare Diagnostics, Inc.
Bivona Uncuffed Wire Endotracheal Tubes,
Smiths Medical ASD Inc.
Concerto User Interface Software provided with the following systems: (1) Xstrahl 100 Electronic Brachytherapy - 100kV Superficial X-Ray Therapy S…
Xstrahl Limited
REF/Catalogue Number GSXE0020, GORE CARDIOFORM SEPTAL OCCLUDER 20 mm Diameter, Catheter Working Length 75 cm, Delivery Profile 10 Fr, STERILE EO, Rx …
W L Gore & Associates, Inc.
REF/Catalogue Number GSX0030A, GORE CARDIOFORM SEPTAL OCCLUDER 30 mm Diameter, Catheter Working Length 75 cm, Delivery Profile 10 Fr, STERILE EO, Rx …
W L Gore & Associates, Inc.
REF/Catalogue Number GSXE0025, GORE CARDIOFORM SEPTAL OCCLUDER 25 mm Diameter, Catheter Working Length 75 cm, Delivery Profile 10 Fr, STERILE EO, Rx …
W L Gore & Associates, Inc.
SIGNA Pioneer nuclear magnetic resonance imaging system
GE Healthcare, LLC
MPR Slotted Mallet, labeling etched onto devices as follows: Medical Products Resource 800.524.5194 www.m-p-r.com MPR-1120-1000 (01)008400014…
Implant Resource Inc
Foundation Kit
Stradis Medical, LLC dba Stradis Healthcare
REF 8420.15.020, Bone Screw/Vite - Ti6AI4V, Self Tapping/Autofilettante, Dia=6.5mm, h=25mm, STERILE R, 2100099, UDI: (01)08033390018852
Limacorporate S.p.A
Optima MR450w 1.5T nuclear magnetic resonance imaging system
GE Healthcare, LLC
1.5T SIGNA HDxt MR System nuclear magnetic resonance imaging system
GE Healthcare, LLC
Herniatome, 17G x 15cm, Lumbar Type, Model Number 5091745
ADRIA SRL
Catalog # BEK4511, Qty: 10, Ecomomy Jamshidi Bone Marrow Biopsy and Aspiration Tray, 11 G X 4"Biopsy/Aspiration needle, 15 G Aspiration Needle (Adjus…
Bard Peripheral Vascular Inc
smiths medical portex Loss of Resistance Device, REF 100/398/000
Smiths Medical ASD Inc.
IUD Insertion Pack
Stradis Medical, LLC dba Stradis Healthcare
6.5MMX165MM CANNULATED SCREW
Smith & Nephew, Inc.
Catalog # BEK3411, Ecomomy Jamshidi Bone Marrow Biopsy Tray, 11 G X 4"Biopsy/Aspiration needle, sterile, Qty: 10, Single Use Only, RX only. Exp. Dat…
Bard Peripheral Vascular Inc
SIGNA Architect nuclear magnetic resonance imaging system
GE Healthcare, LLC
IUD Insertion Kit
Stradis Medical, LLC dba Stradis Healthcare
Easi-Care Gait Belt Metal Buckle (54", 60", and 72" lengths)
Kinsman Enterprises Inc
Cardiosave Li-Ion Battery Pack, Part No. 0146-00-0097. Component of the Cardiosave Hybrid Intra-Aortic Balloon Pump (IABP) with the below Model Numb…
Datascope Corp.
Atellica IM 1600 Analyzer, SMN 11066000
Siemens Healthcare Diagnostics, Inc
SIGNA Creator, SIGNA Explorer nuclear magnetic resonance imaging system
GE Healthcare, LLC
Herniatome, 17G x 9cm, Cervical Type, Model Number 5091749
ADRIA SRL
Canon PET-CT SCANNER, Cartesion Prime, MODEL PCD-1000A
Canon Medical System, USA, INC.
Discovery MR750w 3.0T nuclear magnetic resonance imaging system
GE Healthcare, LLC
EPIQ CVxi Diagnostic Ultrasound Systems, Product Code: 795232
Philips Ultrasound Inc
SIMPLEXA COVID-19 Positive Control Pack, REF MOL4160, IVD, Rx Only, UDI: (01) 20816101027051
DiaSorin Molecular LLC
medfusion Stopcock, 1-way and 4-way, Model Numbers (REF): a. 081-101BE b. 081-101GE c. 081-101GEE d. 081-101NE e. 081-102NE f. 081-102RE g. 08…
Smiths Medical ASD Inc.
SIGNA Voyager nuclear magnetic resonance imaging system
GE Healthcare, LLC
Kit: Central Line Dres Change 20/Cs
Medical Action Industries, Inc. 306
SIGNA Artist nuclear magnetic resonance imaging system
GE Healthcare, LLC
Discovery MR750 3.0T nuclear magnetic resonance imaging system
GE Healthcare, LLC
Tenaculum, Plastic
Stradis Medical, LLC dba Stradis Healthcare
Atellica IM 1300 Analyzer, SMN 11066001
Siemens Healthcare Diagnostics, Inc
Medtronic Sterile single-use blades that are components of the StraightShot M Series Handpiece and Fusion ENT Navigation Software, and the Midas Rex …
Medtronic Xomed, Inc.
HemosIL Liquid Anti-Xa- Automated chromogenic assay for the quantitative determination of unfractionated heparin (UFH) and low molecular weight hepar…
Instrumentation Laboratory
Medtronic sterile single-use blades that are components of the StraightShot M Series Handpiece and Fusion ENT Navigation Software, and the Midas Rex …
Medtronic Xomed, Inc.
REF 8420.15.010, Bone Screw/Vite - Ti6AI4V, Self Tapping/Autofilettante, Dia=6.5mm, h=20mm, STERILE R, 2100099, UDI: (01)08033390018845
Limacorporate S.p.A
Endometrial Biopsy Kit
Stradis Medical, LLC dba Stradis Healthcare
Standard IUD Insertion Kit
Stradis Medical, LLC dba Stradis Healthcare
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.
- 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
Read our methodology - how this data is sourced, computed, and verified.