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 243 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 3 critical (Class I-equivalent) actions, 47 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 Jan 19, 2022 to Feb 2, 2022, covering 30 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).
GE Vscan Extend, being sold as "Vscan Extend Dual Wi-Fi"
GE Healthcare, LLC
Artis icono biplane with software VE20C-diagnostic imaging angiography system Model: 11327600
Siemens Medical Solutions USA, Inc
GE Vscan Extend, being sold as "Vscan Extend Sector USB"
GE Healthcare, LLC
GE Vscan Extend, being sold as "Vscan Extend Sector Wi-Fi"
GE Healthcare, LLC
GE Vscan Extend, being sold as "Vscan Extend Console"
GE Healthcare, LLC
Artis icono floor with software VE20C-diagnostic imaging angiography system Model: 11327700
Siemens Medical Solutions USA, Inc
API ID 32 C Strips, Reference 32200, Rx Only, IVD API ID 32 C is a qualitative standardized system for the identification of yeasts. It uses minia…
Biomerieux Inc
1. Footrest ( use exclusively in combination with Intelli-C devices) 2. Shoulder support ( use exclusively in combination with Intelli-C devices)
NRT X-RAY A/S
8mm FlexDex Needle Driver, Product Code FD-335 ND
FlexDex Inc.
GE Vscan Extend, being sold as "Vscan Extend Dual DICOM"
GE Healthcare, LLC
Trilogy Evo Repair Kit, RP-Trilogy Evo Muffler Assembly, Material Number 1135257 The Trilogy Evo ventilator provides continuous or intermittent po…
Philips Respironics, Inc.
PIVO Blood Collection Device 20G, REF: 202-0005
Velano Vascular
MAGEC 1 System
NuVasive Specialized Orthopedics, Inc.
Infa-Therm Transport Mattress, Reference Number 989805616831 1015
Philips North America Llc
Medtronic HawkOne Directional Atherectomy System, Catalog numbers H1-M and H1-M-INT., Multi-vessel, 6F (2.2 mm) Recommended sheath, 0.014" (0.36 mm) …
ev3 Inc.
SonarMed AirWave Monitor Kit (Monitor, Sensor Cable, Power Cord), Item Code AW-M0001. used with endotracheal tube (ETT)
Covidien, LP
greiner bio-one VACUETTE TUBE, 5 ml LH Lithium Heparin Sep, 13x100 green cap-yellow ring, non-ridged, 24 racks of 50 pcs., 1200 pcs. in total, REF 45…
Greiner Bio-One North America, Inc.
Senior Living Arial Emergency and Nurse Call Systems
Stanley Security Solutions Inc
Medichoice Infant Heel Warmer, Reference # 989805643721 1079906
Philips North America Llc
Draeger Fabius MRI Anesthesia Machine, Catalog Number 8607300
Draeger Medical, Inc.
VITROS Immunodiagnostic Products High Sample Diluent A Reagent Pack
Ortho-Clinical Diagnostics, Inc.
KWIK-STIK 2 Pack, Catalog #0894P; KWIK-STIK 6 Pack, Catalog #0894K; and LYFO DISK, Catalog #0894L; Microsporum canis derived from ATCC 36299.
Microbiologics Inc
1. Sensis, material # 10764561; UDI: 04056869010137 2. Sensis Vibe Hemo, material # 11007641; UDI: 04056869010199 3. Sensis Vibe Combo, material # …
Siemens Medical Solutions USA, Inc
Heel Snuggler, Reference # 989805603411 99047
Philips North America Llc
Gentueri Viral Transport Medium (VTM), Sterile, IVD
Gentueri Inc
Neodent Easypack Helix GM Acqua 3.5X13/Smart 4.5X2.5 Article Number: 138.107
Straumann USA LLC
ARIES HSV 1&2 Assay, Part Number/REF 50-10017
Luminex Corporation
Neodent Easypack Helix GM Acqua 3.5X8/Smart 4.5X2.5 -intended for dental implant Item 138.089
Straumann USA LLC
Infant Heel Warmers w/strap, Reference # 989805603201 1223
Philips North America Llc
Cardinal Infant Heel Warmer, Reference # 989805617251 11470-010T
Philips North America Llc
ImagePilot Versions 1.92 and 1.93-software primarily facilitates processing and presentation of medical images on display monitors for medical diagno…
Konica Minolta Healthcare Americas, Inc.
Medtronic HawkOne Directional Atherectomy System, Catalog numbers H1-S and H1-S-INT, Small Vessel, 6F (2.2 mm) Recommended sheath, 0.014" (0.36 mm) C…
ev3 Inc.
Voyager Rollator-intended as a mechanical walker Model Number: RLEU10xx (RLEU10BL, RLEU10PK, RLEU10WT) RLEU10BL Voyager Rollator Cobalt Blue UPC: 81…
Compass Health Brands (Corporate Office)
SOMATOM Edge Plus-Computed tomography system Model 1026700
Siemens Medical Solutions USA, Inc
Medtronic Custom Perfusion kits, with the following product descriptions and corresponding model numbers: 1. CUSTOM PACK BB10Q85R FILTER (Model B…
Medtronic Perfusion Systems
GLOBAL UNITE REV STEM SZ 10 Product Code: 110010600
DePuy Orthopaedics, Inc.
GLOBAL UNITE STD STEM SZ 16 Product Code: 110016100
DePuy Orthopaedics, Inc.
Disposable Subdermal Needle Electrode, Corkscrew, Single Use, Sterile; Model Numbers TE/S50715-001-C, TE/S50725-001C, and TE/S50715-001.
Technomed Europe
SOMATOM Definition AS-Computed tomography system Model 8098027
Siemens Medical Solutions USA, Inc
SOMATOM Definition Edge -Computed tomography system Model 10590000
Siemens Medical Solutions USA, Inc
Philips Azurion Interventional Fluoroscopic X-ray System with Azurion R2.2 with LUC configuration start-up issue; Azurion R2.2 emergency stop recover…
Philips North America Llc
Electri-Cool II Portable Cold Therapy Unit, Model Number 767, Part Number 86193
Gentherm Medical, LLC
Regard, T AND A - Rogers, sterilized convenience kits
ROi CPS LLC
Instavac Portable Suction Pump, Constant mode (model #757000, Instavac C) and Intermittent mode (model 756000, Instavac I); and Instavac replacement …
Ohio Medical Corporation
GLOBAL UNITE STD STEM SZ 10 Part Number: 110010100
DePuy Orthopaedics, Inc.
OCT-Camera 211 01 A3; Running software iOCT-Control 3 v1.4
Haag-Streit USA Inc
Proteus 235; Version: PTS-8 versions before PTS-8.7.2
Ion Beam Applications S.A.
GLOBAL UNITE STD STEM SZ 12 Product Code: 110012100
DePuy Orthopaedics, Inc.
SOMATOM Confidence -Computed tomography systems Model 10590100
Siemens Medical Solutions USA, Inc
Flat Panel Detector, Model Number: TFP-800A, used with the Alphenix Systems, Item Numbers: INFX-8000V, INFX-8000C, INFX-8000F, and INFX-8000H.
Canon Medical System, USA, INC.
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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.