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 535 of 782

Official website →

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, 39 moderate recalls, and 10 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 28, 2016 to Jan 11, 2017, 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).

Moderate Jan 11, 2017

GalaSHAPE 3D; product code SH3D03, a medium size oval GalaSHAPE" 3D is indicated for use as a bioresorbable scaffold for soft tissue support and to …

Tepha Incorporated

Moderate Jan 11, 2017

PROFEMUR(R) R RASP HANDLE, REF PPW38078, 1 EACH, NON-STERILE, MicroPort Orthopedics, Arlington, TN Instruments support the implantation of implants.…

MicroPort Orthopedics Inc.

Critical Jan 11, 2017

Normal Saline Flush 0.9% USP Sodium Chloride Injection Syringe, 3 ml fill, 5 ml fill and 10 ml fill. Product codes: 1203, 1205, 1210, 1210-BP Prod…

Nurse Assist, Inc

Moderate Jan 11, 2017

G3 Opticage Expandable Interbody Fusion Device, Model No. 9180-00, 9180-01, 9180-06, 9180-07, 9180-17, 9101-00, 9101-06 The Opticage Expandable Inte…

Interventional Spine Inc

Moderate Jan 4, 2017

Prestige VH

GE Healthcare, LLC

Moderate Jan 4, 2017

Precision 500D

GE Healthcare, LLC

Low Jan 4, 2017

Creatinine/Endpoint [Modified Heinegard-Tiderstrom] for IN VITRO DIAGNOSTIC USE in the quantitative determination of analytes. These are CONSUMABLES …

Sterling Diagnostics, Inc.

Moderate Jan 4, 2017

Arthex S3 Arm Sleeve Connector; Catalog Number AR-1650-02; manufactured and distributed between March and November 2016.

Allen Medical Systems, Inc.

Low Jan 4, 2017

Sterling Diagnostics, Inc.Colorimetric SGOT for IN VITRO DIAGNOSTIC USE in the quantitative determination of analytes. These are CONSUMABLES - a cust…

Sterling Diagnostics, Inc.

Moderate Jan 4, 2017

ADVANTX LCA

GE Healthcare, LLC

Moderate Jan 4, 2017

Prestige SI

GE Healthcare, LLC

Moderate Jan 4, 2017

RFX

GE Healthcare, LLC

Moderate Jan 4, 2017

SOMATOM Perspective, Computed tomography x-ray system

Siemens Medical Solutions USA, Inc

Moderate Jan 4, 2017

ADVANTX LCV+

GE Healthcare, LLC

Moderate Jan 4, 2017

Specimen Gate Laboratory 5002-0180, Specimen Gate eReports 5002-0370, Software Version 1.0 Specimen Gate Laboratory is intended for use as a data pr…

PerkinElmer Health Sciences, Inc.

Moderate Jan 4, 2017

NeuViz 64 Multi-slice CT Scanner Systems

Neusoft Medical Systems Co., Ltd.

Moderate Jan 4, 2017

Prestilix

GE Healthcare, LLC

Moderate Jan 4, 2017

Innova 2000

GE Healthcare, LLC

Moderate Jan 4, 2017

Legacy

GE Healthcare, LLC

Moderate Jan 4, 2017

Shimadzu X-ray High Voltage Generator Model No. UD150B-40 on SONIALVISION safire II/17 systems with 0.7/1.2JG326D X-Ray Tube Diagnostic x-ray high…

Shimadzu Medical Systems

Moderate Jan 4, 2017

NIM EMG Endotracheal Tube, 6.0 mm I.D. x 8.8 mm O.D. (27 FR), Reinforced, Sterile, Rx only. Individually packaged.

Medtronic Xomed, Inc.

Low Jan 4, 2017

Enzymatic Cholesterol (Trinder/COD-CEH) for IN VITRO DIAGNOSTIC USE in the quantitative determination of analytes. These are CONSUMABLES - a customer…

Sterling Diagnostics, Inc.

Low Jan 4, 2017

Sterling Diagnostics, Inc., Enzymatic Uric Acid (Uricase Trinder) for IN VITRO DIAGNOSTIC USE in the quantitative determination of analytes. These ar…

Sterling Diagnostics, Inc.

Low Jan 4, 2017

Sterling Diagnostics, Inc., Enzymatic Glucose for IN VITRO DIAGNOSTIC USE in the quantitative determination of analytes. These are CONSUMABLES - a c…

Sterling Diagnostics, Inc.

Moderate Jan 4, 2017

ADVANTX LCLP+

GE Healthcare, LLC

Low Jan 4, 2017

Sterling Diagnostics, Inc., HDL Cholesterol (PEF Method) for IN VITRO DIAGNOSTIC USE in the quantitative determination of analytes. These are CONSUMA…

Sterling Diagnostics, Inc.

Moderate Jan 4, 2017

ADVANTX LCN+

GE Healthcare, LLC

Moderate Jan 4, 2017

SFX

GE Healthcare, LLC

Moderate Jan 4, 2017

Shimadzu X-ray TV System, Catalog No. SONIALVISION G4

Shimadzu Medical Systems

Moderate Jan 4, 2017

NeuViz 128 Multi-slice CT Scanner System with software version 1.0.7.4038+P06 or previous version

Neusoft Medical Systems Co., Ltd.

Moderate Jan 4, 2017

SOMATOM Scope Power, Computed tomography x-ray system

Siemens Medical Solutions USA, Inc

Low Jan 4, 2017

Sterling Diagnostics, Inc., SGPT Colorimetric for IN VITRO DIAGNOSTIC USE in the quantitative determination of analytes. These are CONSUMABLES - a cu…

Sterling Diagnostics, Inc.

Low Jan 4, 2017

Urea Nitrogen/Color BUN (Enzymatic Berthelot) for IN VITRO DIAGNOSTIC USE in the quantitative determination of analytes. These are CONSUMABLES - a cu…

Sterling Diagnostics, Inc.

Moderate Jan 4, 2017

SOMATOM Scope, Computed tomography x-ray system

Siemens Medical Solutions USA, Inc

Low Jan 4, 2017

Sterling Diagnostics, Inc. Serum Iron/IBC (Colorimetric) for IN VITRO DIAGNOSTIC USE in the quantitative determination of analytes. These are CONSUMA…

Sterling Diagnostics, Inc.

Moderate Jan 4, 2017

VITROS Immunodiagnostic Products Intact PTH Reagent Pack: 1) UPN 10758750006287 / Product Code 6802892 - Reagent Pack, 2) UPN 10758750006250 / Produ…

ORTHO-CLINICAL DIAGNOSTICS

Moderate Jan 4, 2017

Prestige II

GE Healthcare, LLC

Moderate Dec 28, 2016

Tibial Component Fixed Hinge Small Long; Tibial Component Fixed Hinge Small Short The product is a component is a systems that is intended for the r…

Stanmore Implants Worldwide Ltd.

Moderate Dec 28, 2016

Best Practices kits containing certain production lots of Clearify Visualization System Item Code: 21-345 Intended to be used prior to and during …

Medtronic

Moderate Dec 28, 2016

K-Wire 1.4mm x 12in Non-Threaded, Part Number 9080-12U; K-Wire Threaded 1.4mm x 18, Part Number 9080-18T; K-Wire Non-Threaded 1.4mm x 18, Part Number…

Amendia, Inc

Moderate Dec 28, 2016

Ultroid Hemorrhoid Management Systems 110/220 VAC and procedures kit including the Ultroid Disposable Sterile Probes

Ultroid Technologies, Inc.

Moderate Dec 28, 2016

OSCOR ADELANTE BREEZWAY 10F STRAIGHT S79CM D84CM Catalog # AB101219 Is designed to facilitate the introduction of catheters to any of the heart ch…

Oscor, Inc.

Moderate Dec 28, 2016

BD SurePathTM Preservative Collection Vials, catalog numbers 490505, 490527, 491095, 491096, and 491097. SurePath¿ Preservative Fluid is designed…

Becton Dickinson & Co.

Moderate Dec 28, 2016

MEDTRONIC ARRIVE BRAIDED TRANSSEPTAL SHEATH 10F C90¿ S79CM D84CM GLOBAL Catalog # 990079-090-000 Is designed to facilitate the introduction of cat…

Oscor, Inc.

Moderate Dec 28, 2016

CyberKnife Robotic Radiosurgery Systems, models: G3, G4, VSI. Radiology: The CyberKnife Robotic Radiosurgery System is indicated for treatment pla…

Accuray Incorporated

Moderate Dec 28, 2016

BIOMET 3i LOW PROFILE 17¿ ABUTMENT 4.1MM(D) X 4MM(H) An endosseous dental implant abutment is a premanufactured prosthetic component directly connec…

Biomet 3i, LLC

Moderate Dec 28, 2016

Femoral Integral Shaft & Stem 15x27 HA Coated; Femoral Integral Shaft & Stem 15x30 HA Coated; Femoral Integral Shaft & Stem 30x27 HA Coated; Fe…

Stanmore Implants Worldwide Ltd.

Moderate Dec 28, 2016

8470-009-040 4.0MM Precision Round, 16CM, single use, Sterile The Stryker MIS (Minimally Invasive Surgery) product offering, is used to remove osseo…

Stryker Instruments Div. of Stryker Corporation

Moderate Dec 28, 2016

Black Widow 6.6mm x 20mm Screw, Part Number TBS020; Black Widow 6.6mm x 25mm Screw, Part Number TBS025; Black Widow 6.6mm x 30mm Screw, Part Number T…

Amendia, Inc

Low Dec 28, 2016

ANGIODYNAMICS Percutaneous Introducer Set under the following labels: 1) 4 F Stiffened Micro-Introducer Kit, 45CM SS/T NON-ECHO S PG, Item Number H78…

Angiodynamics, Inc.

Nearby Agencies

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

Compare FDA Medical Devices with FDA Food Safety →

Learn More About Recalls

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.