PlainRecalls

Product category · Updated Jul 29, 2026

Medical Devices recalls

Medical device recalls including implants, diagnostic equipment, and surgical tools

Total recalls
40,910
Top agency
FDA Devices
Years covered
2000–2026
Check a product → All categories

Medical Devices ranks #1 of 12 among PlainRecalls categories by recall count (40,910 notices, 39.3% of the archive); 9% of graded records are high-severity.

The FDA, CPSC and NHTSA have published 40,910 medical devices recalls between 2000 and 2026 - roughly 39.3% of the 104,158-record archive. Among 12 product categories, that is #1 of 12. Of the 40,910 records graded for severity, 9% are high-severity. Most are issued by FDA Devices. Counts reflect market size and reporting activity, not a product's inherent danger.

  • 40,910 total recalls
  • #1 of 12 among categories
  • 9% graded high-severity
  • FDA Devices top agency

Category snapshot

According to PlainRecalls' category ranking (distinct recall events, same sort as /category), Medical Devices is #1 of 12 (1st of 12) with 40,910 recalls, about 39.3% of the 104,158-record federal archive, with 3,645 graded high-severity, most issued by FDA Devices.

40,910
total recalls
#1 of 12
category rank by events
9%
graded high-severity
FDA Devices
top issuing agency

Medical Devices recalls by year

2000–2026

0 1000 2000 3000 4000 2015 2016 2017 2018 2019 2020 2021 2022 2023 2024 2025 2026 2576 3437 2649 3803 3003 3209 2356 2247 2606 3417 2982 1787

Source: FDA · CPSC · NHTSA As of Jul 29, 2026

Severity distribution

Graded records only

recalls
Source FDA / CPSC severity classification

Recalls by issuing agency

recalls
Source PlainRecalls index of federal feeds

Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.

Recalls in Medical Devices

Newest first · Page 236 of 819

FDA Devices Moderate Sep 14, 2022

VITROS XT 7600 Integrated System with Version 3.7.2 and below Product Code: 6844461

Ortho-Clinical Diagnostics, Inc.

FDA Devices Moderate Sep 14, 2022

Product Description/Item: ChemoLock Vial Spike, 20mm/011-CL-80S; ChemoLock Bag Spike/CL-10; ChemoLock w/Mini Bag Spike/CL-17; 8 IN (20cm) APPX 1.0…

ICU Medical, Inc.

FDA Devices Critical Sep 14, 2022

Philips OmniLab Advanced+ Intl (Flow Gen), Rx Only. To provide noninvasive ventilation support for patients with obstructive sleep apnea syndrome (O…

Philips Respironics, Inc.

FDA Devices Moderate Sep 14, 2022

Various neurology packs

American Contract Systems, Inc.

FDA Devices Moderate Sep 14, 2022

Various Pacemaker Packs, Cardio Thoracic Packs

American Contract Systems, Inc.

FDA Devices Critical Sep 14, 2022

Philips OmniLab Advanced + with Heated Tube Humidifier, Rx Only. To provide noninvasive ventilation support for patients with obstructive sleep apne…

Philips Respironics, Inc.

FDA Devices Moderate Sep 14, 2022

Orthex External Fixation Wire Sharp Bayonet 1.8 x 400 mm Model: K400-18BN

OrthoPediatrics Corp

FDA Devices Moderate Sep 14, 2022

Medline CHEST TUBE REORDER NO: DYNJ36762A

Medline Industries Inc.

FDA Devices Moderate Sep 14, 2022

Various ENT Packs

American Contract Systems, Inc.

FDA Devices Moderate Sep 14, 2022

VITROS XT 3400 Chemistry System with Version 3.7.2 and below Product Code: 6844458

Ortho-Clinical Diagnostics, Inc.

FDA Devices Moderate Sep 14, 2022

Insertion Kit for use with SENSATION PLUS 8F. 50cc Intra-Aortic Balloon Catheter

Datascope Corporation

FDA Devices Moderate Sep 14, 2022

Various Angiography/Cath Lab packs/trays

American Contract Systems, Inc.

FDA Devices Critical Sep 14, 2022

Philips BiPAP A40, Rx Only. To provide noninvasive ventilation support for patients with obstructive sleep apnea syndrome (OSA) and respiratory insu…

Philips Respironics, Inc.

FDA Devices Moderate Sep 14, 2022

Abbott Alinity m SARS-CoV-2 CTRL Kit, REF 09N78-085, each kit contains 12 x 1.3mL CTRL - and 12 x 1.3 mL CTRL +, For In Vitro Diagnostic Use.

Abbott Molecular, Inc.

FDA Devices Moderate Sep 14, 2022

Various Cysto Packs

American Contract Systems, Inc.

FDA Devices Moderate Sep 14, 2022

Various hysterectomy, vaginal packs

American Contract Systems, Inc.

FDA Devices Moderate Sep 14, 2022

CARTO VIZIGO 8.5F Bi-Directional Guiding Sheath, REF: D138501. Used to introduce various cardiovascular catheters into the heart.

Biosense Webster, Inc.

FDA Devices Critical Sep 14, 2022

Philips OmniLab Advanced+, Rx Only. To provide noninvasive ventilation support for patients with obstructive sleep apnea syndrome (OSA) and respirat…

Philips Respironics, Inc.

FDA Devices Moderate Sep 14, 2022

Optima Coil System Model OPTI0520CSF10. For endovascular embolization.

BALT USA, LLC

FDA Devices Moderate Sep 14, 2022

Various Laparoscopy Packs

American Contract Systems, Inc.

FDA Devices Moderate Sep 14, 2022

Various PICC Line, Central Line Packs

American Contract Systems, Inc.

FDA Devices Moderate Sep 7, 2022

Aesculap ENNOVATE SET SCREW STERILE-implants are used for dorsal monosegmental and multisegmental stabilization of the lumbar, thoracic and sacral sp…

Aesculap Implant Systems LLC

FDA Devices Moderate Sep 7, 2022

Pentacam AXL REF 70100, Pentacam HR REF 70900. Used to image the anterior segment of the eye.

Oculus Optikgeraete GMBH

FDA Devices Moderate Sep 7, 2022

DeRoyal Sterile Custom Kits containing ICU Medical MicroClave Clear Connectors

DeRoyal Industries Inc

FDA Devices Moderate Sep 7, 2022

Artis icono biplane- Model No. 11327600 Artis icono floor- Model No. 11327700

Siemens Medical Solutions USA, Inc

FDA Devices Moderate Sep 7, 2022

ARCHITECT STAT Troponin-I Reagent Kit, REF 2K41-27

Abbott Laboratories

FDA Devices Moderate Sep 7, 2022

VITEK 2 / MYLA VITEK 2 Software versions 8.01, 8.02 (veterinary use only), 9.01, 9.02, 9.03 MYLA Software versions V4.8 and V4.9

bioMerieux, Inc.

FDA Devices Moderate Sep 7, 2022

T-Cell Xtend REF TTK.610 US

OXFORD IMMUNOTEC LTD

FDA Devices Moderate Sep 7, 2022

The PRM is intended to be used as part of the ZOOM LATITUDE Programming System to communicate with Boston Scientific implantable pulse generators. Th…

Boston Scientific Corporation

FDA Devices Moderate Sep 7, 2022

Dimension Vista LOCI CA 15-3 Flex reagent cartridge. In Vitro Diagnostic for the quantitative measurement of CA 15-3. Siemens Material Number (SMN…

Siemens Healthcare Diagnostics, Inc.

FDA Devices Moderate Sep 7, 2022

FGFR RGQ RT-PCR Kit (RUO, not IVD) REF 8747010

Qiagen Sciences LLC

FDA Devices Moderate Sep 7, 2022

DigitalDiagnost C50 1.1

Philips North America Llc

FDA Devices Moderate Sep 7, 2022

AggreGuide A-100 Instrument

Aggredyne, Inc.

FDA Devices Moderate Sep 7, 2022

T-SPOT.TB REF TB.300 US

OXFORD IMMUNOTEC LTD

FDA Devices Moderate Sep 7, 2022

INFX-8000V. For radiographic and fluoroscopic studies and intervention.

Canon Medical System, USA, INC.

FDA Devices Moderate Sep 7, 2022

Metalogix Self-Drill Half-Pin, a component of the Revolution External Fixation System. Orthopedic. Metalogix Self-Drill Half-Pin 5x30x215mm RE…

New Standard Device Inc

FDA Devices Critical Sep 7, 2022

NIM EMG Endotracheal Tube, Part Numbers: a) REF 8229308 b) REF 8229307 c) REF 8229306

Medtronic Xomed, Inc.

FDA Devices Moderate Sep 7, 2022

therascreen FGFR RGQ RT-PCR Kit (CE IVD, not sold in the US) REF 874711

Qiagen Sciences LLC

FDA Devices Critical Sep 7, 2022

NIM CONTACT EMG Endotracheal Tube, Part Numbers: a) REF 8229508 b) REF 8229507 c) REF 8229506

Medtronic Xomed, Inc.

FDA Devices Moderate Sep 7, 2022

Pentacam AXL Wave REF 70020. Used to image the anterior segment of the eye.

Oculus Optikgeraete GMBH

FDA Devices Moderate Sep 7, 2022

AIM-V Medium REF AV.200/500

OXFORD IMMUNOTEC LTD

FDA Devices Moderate Sep 7, 2022

Artis Q floor- Model No. 10848280 Artis Q ceiling- Model No. 10848281 Artis Q biplane- Model No. 10848282 Artis Q zeego- Model No. 10848283 Artis…

Siemens Medical Solutions USA, Inc

FDA Devices Moderate Sep 7, 2022

Artis pheno- Model No. 10849000

Siemens Medical Solutions USA, Inc

FDA Devices Moderate Sep 7, 2022

Pentacam HR REF 70900. Used to image the anterior segment of the eye.

Oculus Optikgeraete GMBH

FDA Devices Moderate Sep 7, 2022

The PRM is intended to be used as part of the ZOOM LATITUDE Programming System to communicate with Boston Scientific implantable pulse generators. Th…

Boston Scientific Corporation

FDA Devices Moderate Sep 7, 2022

therascreen FGFR RGQ RT-PCR kit (US IVD) REF 874721

Qiagen Sciences LLC

FDA Devices Critical Sep 7, 2022

NIM EMG Endotracheal Tube, Part Numbers: a) REF 8229307J b) REF 8229308J c) REF 8229306J

Medtronic Xomed, Inc.

FDA Devices Moderate Sep 7, 2022

The Programmer/Recorder/Monitor (PRM) is intended to be used as part of the ZOOM LATITUDE Programming System to communicate with Boston Scientific im…

Boston Scientific Corporation

FDA Devices Moderate Sep 7, 2022

TaperFit Stem, Size 0, 38mm OFFSET, 12/14 Taper + 188.550 Centraliser, For Cemented Use, REF 588.3800. Orthopedic hip implant component.

Corin Ltd

FDA Devices Moderate Sep 7, 2022

EverFlex Self-Expanding Peripheral Stent with Entrust Delivery System

Medtronic Inc.

What to do with this

Monitoring medical devices? Start here.

  • Check a specific product against the full federal archive before you use or buy it. Recall checker
  • Most medical devices recalls come from FDA Devices - browse that agency's full feed. FDA Devices recalls
  • Sort the whole archive by severity to see the highest-risk active recalls first. Rankings

Recall categorization follows the issuing agency's product taxonomy; always confirm specifics on the official notice.

Nearby categories

Adjacent product categories that share hazard patterns or regulatory oversight.

Data sources

Category data as of Jul 29, 2026.

Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. Category counts and the year trend are computed across the full archive for medical devices. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of Jul 29, 2026.