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 729 of 782

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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 6 critical (Class I-equivalent) actions, 41 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 Aug 21, 2013 to Aug 28, 2013, 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 Aug 28, 2013

GENESIS(R) II CRUCIATE RETAINING ARTICULAR INSERT, TRIAL, SIZE 3-4, A/P 48 MM, M/L 68 MM, QTY 1, NON-STERILE, REF 71430490, Product Usage: Ortho…

Smith & Nephew Inc

Moderate Aug 28, 2013

00597503110 Provisional AC ARTSURF PROV 34/STRIPE YEL10, Rx, Sterile; 00597503112 Provisional AC ARTSURF PROV 34/STRIPE YEL12, Rx, Sterile; 0…

Zimmer, Inc.

Moderate Aug 28, 2013

65597201333 Femur CR POR FEM SURF HDN HATCP CML, Rx, Sterile; 65597201334 Femur CR POR FEM SURF HDN HATCP CMR, Rx, Sterile; 65597201433 Femur C…

Zimmer, Inc.

Moderate Aug 28, 2013

00597106126 Provisional ALL POLY PAT PROV MICRO SZ 26, Rx, Sterile; 00597106129 Provisional ALL POLY PAT PROV MICRO SZ 29, Rx, Sterile; 00597…

Zimmer, Inc.

Moderate Aug 28, 2013

00587806126 Patella MICRO POROUS PAT 26MM X 10MM, Rx, Sterile; 00587806129 Patella MICRO POROUS PAT 29MM X 10MM, Rx, Sterile; 00587806132 Pate…

Zimmer, Inc.

Moderate Aug 28, 2013

00595201201 Femur CR-FLEX POR FEM B-L Rx, Sterile; 00595201202 Femur CR-FLEX POR FEM B-R Rx, Sterile; Used in total knee arthroplasty and i…

Zimmer, Inc.

Moderate Aug 28, 2013

00595001201 Femur CR-FLEX PCT FEM B-L Rx, Sterile; 00595001202 Femur CR-FLEX PCT FEM B-R Rx, Sterile; Used in t…

Zimmer, Inc.

Moderate Aug 28, 2013

Product Name: nanoPOINT Injector System, item number 37-0000-08. Intended to fold and insert a STAAR Surgical Collamer¿ nanoFLEX or Afinity IOLs, …

Medicel Ag

Moderate Aug 28, 2013

00597604110 Articular Surface AC ART SURF 56/STRIPED GRN 10, Rx, Sterile; 00597604112 Articular Surface AC ART SURF 56/STRIPED GRN 12, Rx, Sterile…

Zimmer, Inc.

Moderate Aug 28, 2013

PleuraGuide Disposable Chest Tube Kit; Product codes: 17100, 17150, and 17200. Indicated to assist with the insertion of thoracic catheters.

Atrium Medical Corporation

Moderate Aug 28, 2013

90595204117 Articular Surface XLPE CR ART SURF AE56/STGRN 17, Rx, Sterile; 90595204120 Articular Surface XLPE CR ART SURF AE56/STGRN 20, Rx, Steri…

Zimmer, Inc.

Moderate Aug 28, 2013

Edwards Lifesciences Suction Wand Model S099B, packaged in Sorin Group Heart/Lung Perfusion Packs.

Sorin Group USA, Inc.

Moderate Aug 28, 2013

65597201131 Femur CR POR FEM SURF HDN HATCP AML Rx, Sterile; 65597201132 Femur CR POR FEM SURF HDN HATCP AMR Rx, Sterile; 65597201231 Femur CR…

Zimmer, Inc.

Moderate Aug 28, 2013

Stryker Visum 300 Ceiling-mounted Exam Light.

Stryker Communications

Moderate Aug 28, 2013

00597001131 Femur CR PRC SURF HDN FEM CO-NID AML, Rx, Sterile; 00597001132 Femur …

Zimmer, Inc.

Moderate Aug 28, 2013

The Discovery NM/CT 570c CT Standalone Scan The Discovery NM/CT 570c hybrid system is a combination of a cardiac dedicated nuclear imaging subsys…

GE Healthcare, LLC

Moderate Aug 28, 2013

90595203117 Articular Surface XLPE CR ART SURF AE34/STYEL 17, Rx, Sterile; 90595203120 Articular Surface XLPE CR ART SURF AE34/STYEL 20, Rx, Steri…

Zimmer, Inc.

Moderate Aug 28, 2013

Boston Scientific, ENERGEN DR ICD, Model E143. The device is an Implantable Cardioverter Defibrillator.

Boston Scientific CRM Corp

Moderate Aug 28, 2013

Distributed in USA: Product Number: 40-2894: Reinforced Wound Closure, Latex Free Sterile EO Rx, 1/4" X 4 ", 6 mm X100 mm, (2 Cards/pouch, 1,00…

Aspen Surgical Products, Inc.

Low Aug 28, 2013

ConvaTec Flexi-Seal SIGNAL Fecal Management System, Rx Only Product Usage: For use to manage fecal incontinence through the collection of liquid …

Convatec Inc.

Moderate Aug 21, 2013

CELLTRACKS AUTOPREP System (Software Version 2.4.1 & Below. Product Usage: The CELLTRACKS AUTOPREP System is a general purpose laboratory instr…

Veridex, LLC

Moderate Aug 21, 2013

3.2mm Drill Bit. This is a component within the PediLoc Locking Plate System utilized to pre-drill a hole in bone prior to placement of a bone screw.

OrthoPediatrics Corp

Moderate Aug 21, 2013

100/120V AC, Advanced Perfusion System 1 Product Usage: The Terumo¿ Advanced Perfusion System 1 is indicated for use in extracorporeal circulatio…

Terumo Cardiovascular Systems Corporation

Critical Aug 21, 2013

Nova Max Glucose Test Strips (100 Count Retail Canada)Catalog Number: 43955 Product Usage: The Nova Max Glucose Test Strips are for use with th…

Nova Biomedical Corporation

Moderate Aug 21, 2013

Terumo¿ Advanced Perfusion System 1 (APS1, System 1) Description: 220/240V AC Product Usage: The Terumo¿ Advanced Perfusion System 1 is indicate…

Terumo Cardiovascular Systems Corporation

Critical Aug 21, 2013

Nova Max Glucose Test Strips (50 Count International Catalog Number: 45512 Product usage: The Nova Max Glucose Test Strips are for use with the …

Nova Biomedical Corporation

Moderate Aug 21, 2013

Biomet 3i Dental Implant, Non-Platform Switched Parallel Walled Implant 5mm (D) x 13mm (L)

Biomet 3i, LLC

Moderate Aug 21, 2013

Siemens AXIOM Artis zeego x-ray, angiographic system

Siemens Medical Solutions USA, Inc

Moderate Aug 21, 2013

C-QUR Edge Mesh (All sizes and shapes). Intended for use in soft tissue deficiencies.

Atrium Medical Corporation

Critical Aug 21, 2013

Nova Max Glucose Test Strips (10 Count Canada)Catalog Number: 43877 Product The Nova Max Glucose Test Strips are for use with the Nova Max Family …

Nova Biomedical Corporation

Moderate Aug 21, 2013

ISE Electrolyte Reference reagent (for Synchron LX Systems and UniCel DxC 600/800 Systems), Part No. A28937, A28945, 467935, 467915. Product Usage…

Beckman Coulter Inc.

Critical Aug 21, 2013

Nova Max Plus Monitor System (Kit w/10 Count Vials International) Catalog Number: 45507 Product Usage: The Nova Max Glucose Test Strips are for …

Nova Biomedical Corporation

Moderate Aug 21, 2013

Biomet 3i Dental Implant, Parallel Walled 6mm (D) x 10mm (L)

Biomet 3i, LLC

Moderate Aug 21, 2013

Disposable Temperature Probes, (sterile), Sensor diameter: 3mm/0.12 in; 25 units per box. Vital Signs Inc. a GE Healthcare Company, 20 Campus Road, T…

Vital Signs Devices, a GE Healthcare Company

Moderate Aug 21, 2013

Colorimetric (CM)/ Rate (RT) incubator wear pads. Product Codes: 1) 6801375, 2) 6801890, 3) 6802445, 4) 6802413 Product Usage: The CM/RT incubat…

Ortho-Clinical Diagnostics

Low Aug 21, 2013

ADVIA Centaur Calibrator A. Cat. #04800735, SMN 10285904 (6 pack); Cat. # 04800840, SMN 10285905 (6 pack - REF). For calibrating the following …

Siemens Healthcare Diagnostics, Inc

Low Aug 21, 2013

Remel X/pect Flu A&B Control Swabs, For In Vitro Diagnostic Use, Ref R246003, each package contains 20 Flu A Control Swabs and 20 Flu B Control Swab…

Remel Inc

Moderate Aug 21, 2013

C-QUR V-Patch Mesh (All sizes and shapes). Intended for use in soft tissue deficiencies.

Atrium Medical Corporation

Critical Aug 21, 2013

Nova Max Glucose Test Strips (10 Count Vials) Catalog Number: 43604 These strips are kitted into Nova Max Glucose Test Strip System Kits 43435 and …

Nova Biomedical Corporation

Moderate Aug 21, 2013

C-QUR Mesh (All Sizes, shapes). Intended for use in soft tissue deficiencies.

Atrium Medical Corporation

Moderate Aug 21, 2013

CELLTRACKS ANALYZER II (Software Version 2.5.1 & Below. Product Usage: The CELLTRACKS AUTOPREP System is a general purpose laboratory instrumen…

Veridex, LLC

Moderate Aug 21, 2013

GE LightSpeed CT750 HD The GE LightSpeed CT750 HD Computed Tomography X-ray system is intended to produce cross-sectional images of the body by co…

GE Healthcare, LLC

Moderate Aug 21, 2013

Arrow International, Inc. Two-Lumen CVC Kit with Blue Flex Tip Catheter. The multiple lumen catheter permits venous access to the central circulation…

Arrow International Inc

Moderate Aug 21, 2013

SIGNA INFINITY MR SYSTEM WITH EXCITE TECHNOLOGY GE 3.0T SIGNA INFINITY TWINSPEED WITH EXCITE MR SYSTEM GE SIGNA 3.0T WITH EXCITE MR SYSTEM GE SI…

GE Healthcare, LLC

Moderate Aug 21, 2013

REF 00-4309-071-36 Trabecular Metal Reverse Shoulder System Instrumentation, Glenosphere Helmet, 36 mm Diameter Nonsterile, Qty -1 Instrumentation…

Zimmer, Inc.

Moderate Aug 21, 2013

220/240V AC, Advanced Perfusion System 1 Product Usage: The Terumo¿ Advanced Perfusion System 1 is indicated for use in extracorporeal circulatio…

Terumo Cardiovascular Systems Corporation

Moderate Aug 21, 2013

Siemens syngo.plaza SW version VA20 with Mammography license. image processing, radiological system

Siemens Medical Solutions USA, Inc

Moderate Aug 21, 2013

Terumo¿ Advanced Perfusion System 1: 220/240V AC, Advanced Perfusion System 1 The Terumo¿ Advanced Perfusion System 1 is indicated for use in ext…

Terumo Cardiovascular Systems Corporation

Moderate Aug 21, 2013

Medtronic Affinity Pediatric Arterial Filter, model number S4014, sterilized using ethylene oxide. Recall Update 9/6/13: Medtronic, Red cross In…

Medtronic Inc. Cardiac Rhythm Disease Management

Critical Aug 21, 2013

Nova Max Plus Monitor System (Kit w/10 Count Vials) Catalog Number: 43435 Product usage: The Nova Max Glucose Test Strips are for use with the N…

Nova Biomedical Corporation

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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.