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 482 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 2 critical (Class I-equivalent) actions, 46 moderate recalls, and 2 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 10, 2018 to Jan 24, 2018, 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 Jan 24, 2018

VALITUDE X4 CRT-P Pacemaker

Boston Scientific Corporation

Moderate Jan 24, 2018

Aspire HD Plus (FDR MS-2500), also known as Aspire HD Plus F and Aspire HD-s (FDR MS-2000), also known as Aspire HD Plus S). Mammography machine …

Fujifilm Medical Systems U.S.A., Inc.

Moderate Jan 24, 2018

ESSENTIO EL DR Pacemaker

Boston Scientific Corporation

Moderate Jan 24, 2018

TRYPTIK(R) 2 C-PLATE SELF-TAPPING POLYAXIAL SCREW 4.0 MM, LENGTH 16 MM, REF TRY-PS-40 16-S, Qty 2 TRYPTIK(R) 2C-Plate Anterior Cervical Plate Sys…

SPINEART SA

Moderate Jan 24, 2018

VISIONIST X4 CRT-P Pacemaker

Boston Scientific Corporation

Moderate Jan 24, 2018

Affirm Lateral Arm Upright Biopsy Accessory. Product Number: ASY-09880

Hologic, Inc.

Moderate Jan 24, 2018

PROPONENT VDD SL Pacemaker

Boston Scientific Corporation

Moderate Jan 24, 2018

TRYPTIK(R) 2 C-PLATE SELF-TAPPING POLYAXIAL SCREW 4.5 MM, LENGTH 14 MM, REF TRY-PS-45 14-S, Qty 2 TRYPTIK(R) 2C-Plate Anterior Cervical Plate Sys…

SPINEART SA

Moderate Jan 24, 2018

ALTRUA 2 DR Pacemaker

Boston Scientific Corporation

Moderate Jan 24, 2018

Fellows "Mighty 8" Power strip (Part Number 04175-0008) and TrippLite Power strip (PS-415-HGULTRA - Part Number 13-00106-00) are two components sold …

Merge Healthcare, Inc.

Moderate Jan 24, 2018

Intellicuff Standalone (PN 951001) Used to continuously measure and automatically maintain the user-set cuff pressure of an endotracheal tube or t…

Hamilton Medical, Inc.

Moderate Jan 24, 2018

Medtronic KYPHON(R) Express(TM) Directional Bone Filler Device, SIZE 2, REF FB, QTY 1 EA, Rx only STERILE R

Medtronic Sofamor Danek USA Inc

Moderate Jan 24, 2018

ESSENTIO MRI DR Pacemaker

Boston Scientific Corporation

Moderate Jan 24, 2018

Persona Partial Knee System, Size 8, Finishing Guide

Zimmer Biomet, Inc.

Moderate Jan 24, 2018

Brilliance 64, (Code 728231) Intended to produce images of the head and body by computer reconstruction of x-ray transmission data taken at differ…

Philips Medical Systems (Cleveland) Inc

Moderate Jan 24, 2018

PROPONENT MRI Pacemaker

Boston Scientific Corporation

Moderate Jan 17, 2018

Freedom60 Precision Flow Rate Tubing Sets, REF/Part Numbers F900, F2400, F60, F10, F275, F600, F45, F1200 F180.

Repro-Med Systems, Inc.

Moderate Jan 17, 2018

Mac Pin Non-Cannulated Screw, 6.5 x 60mm

Amendia, Inc

Moderate Jan 17, 2018

Mobile Mini C-arm system Part # 1000-0004. Intended to provide the physician with general fluoroscopic visualization of the patient, including, b…

Orthoscan, Inc.

Moderate Jan 17, 2018

EMPOWR Porous Knee System TIBIAL PUNCH, SMALL, REF 801-05-202, NON STERILE, Qty 1 For use in orthopedic surgery.

Encore Medical, Lp

Moderate Jan 17, 2018

Brainlab Navigation System Spine & Trauma 3D with component Brainlab DrapeLink Registration Kit for C-arm Zeihm Vision RFD: Adapter Left

Brainlab AG

Moderate Jan 17, 2018

Mobile Mini C-arm system Part # 1000-0004-FD. Intended to provide the physician with general fluoroscopic visualization of the patient, including,…

Orthoscan, Inc.

Moderate Jan 17, 2018

Philips Healthcare Brilliance iCT computed tomography x-ray system

Philips Medical Systems (Cleveland) Inc

Moderate Jan 17, 2018

Alaris PCA Pump, Model 8120. The firm name on the label is CareFusion. The Alaris Syringe Pump module and Alaris PCA module are infusion pump mod…

CareFusion 303, Inc.

Moderate Jan 17, 2018

Cordis S.M.A.R.T. Flex Biliary Stent System Product Usage: Is indicated for use in the palliation of malignant strictures in the biliary tree.

Cordis Corporation

Moderate Jan 17, 2018

HIgH-Flo Subcutaneous Safety Needle Sets, 2-Needle Set/ 24 Gauge 9mm Needles, REF/Part Numbers RMS22606, RMS22609, RMS22612, RMS12606, RMS22409, RMS…

Repro-Med Systems, Inc.

Critical Jan 17, 2018

Certitude Delivery System and any associated Multipacks Models - 9600CT20A, 9600CT23A, 9600CT26A, 9600CT29A Product Usage: The Edwards Certitude …

Edwards Lifesciences, LLC

Moderate Jan 17, 2018

Philips Healthcare Brilliance iCT SP computed tomography x-ray system

Philips Medical Systems (Cleveland) Inc

Moderate Jan 17, 2018

DJO EMPOWR KNEE LOCKING TIBIAL PUNCH GUIDE, REF 801-05-042, NON STERILE, Qty 1 For use in orthopedic surgery.

Encore Medical, Lp

Critical Jan 17, 2018

LIFEPAK 20e DEFIBRILLATOR/MONITOR, 3201273 Product Usage: The LIFEPAK 20e defibrillator/monitor is intended for use in the hospital, physician s …

Physio-Control, Inc.

Moderate Jan 17, 2018

Mobile Mini C-arm system Part # 1000-0001. Intended to provide the physician with general fluoroscopic visualization of the patient, including, b…

Orthoscan, Inc.

Moderate Jan 17, 2018

Philips Healthcare IQon Spectral CT computed tomography x-ray system

Philips Medical Systems (Cleveland) Inc

Moderate Jan 17, 2018

Sundream 12 V tanning bed

ProSun International, LLC

Moderate Jan 17, 2018

Mobile Mini C-arm system Part # 1000-0005. Intended to provide the physician with general fluoroscopic visualization of the patient, including, b…

Orthoscan, Inc.

Moderate Jan 17, 2018

Alaris Syringe Pump, Model 8110. The firm name on the label is CareFusion. The Alaris Syringe Pump module and Alaris PCA module are infusion pump…

CareFusion 303, Inc.

Moderate Jan 17, 2018

EMPOWR Porous Knee System TIBIAL PUNCH, MEDIUM, REF 801-05-203, NON STERILE, Qty 1 For use in orthopedic surgery.

Encore Medical, Lp

Moderate Jan 17, 2018

CombiDiagnost R90 Image-Intensified fluoroscopic x-ray system CombiDiagnost R90 is a multi-functional general R/F system. It is suitable for all r…

Philips Electronics North America Corporation

Moderate Jan 17, 2018

EMPOWR Porous Knee System TIBIAL PUNCH, LARGE, REF 801-05-204, NON STERILE, Qty 1 For use in orthopedic surgery.

Encore Medical, Lp

Moderate Jan 17, 2018

UNIVERSAL FLEX2 BREATHING CIRCUIT, Item Numbers: D460-6133Z, D390-6121Z, D390-6121Z, D495-61Z, DF4116-6121Z, D466-61Z, DFP170-6121, DF3115-6121Z, DF3…

King Systems Corp. dba Ambu, Inc.

Moderate Jan 10, 2018

RED SEXP DSTL FEM 19CM RT ASSY, model # CP111817

Zimmer Biomet, Inc.

Moderate Jan 10, 2018

CER OPTION TYPE 1 TPR SLEVE -6, model # 650-1064

Zimmer Biomet, Inc.

Moderate Jan 10, 2018

CADD-Legacy 1, Model 6400 Ambulatory Infusion Pump, REF 21-6400-51, PC 10008552-001, Smiths Medical ASD, Inc. Rx ONLY

Smiths Medical ASD Inc.

Moderate Jan 10, 2018

Euro Diagnostica DIASTAT ANA (anti-nuclear antibody) ELISA DIASTAT ANA (anti-nuclear antibody) A positive ANA test result provides presumptive evi…

Euro Diagnostica AB

Low Jan 10, 2018

Access 2 Immunoassay System, Catalog Number 81600N. In vitro diagnostic device used for the quantitative, semi-quantitative, or qualitative determ…

Beckman Coulter Inc.

Moderate Jan 10, 2018

Lateral Troch Plate Full Crimp - 254mm, model # 350838

Zimmer Biomet, Inc.

Moderate Jan 10, 2018

PPS RingLoc+ Acetabular Shell, RNGLC+ LTD HOLE SHELL SZ62 The Porous Plasma Spray (PPS) Ringloc¿+ Acetabular System is intended to replace the na…

Zimmer Biomet, Inc.

Moderate Jan 10, 2018

COMP 12MM HUM FRAC STEM MACRO, model # 11-113562

Zimmer Biomet, Inc.

Moderate Jan 10, 2018

OSS CEMENTED IM STEM 12X150, model # 150366

Zimmer Biomet, Inc.

Low Jan 10, 2018

UniCel DxC 600i SYNCHRON Access Clinical Systems; A25656, A25638. In vitro diagnostic device used for the quantitative, semi-quantitative, or qual…

Beckman Coulter Inc.

Moderate Jan 10, 2018

RED SEXP DSTL FEM 19CM LT ASSY, model # CP111828

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.