PlainRecalls

Product category · Updated Jul 2, 2026

Medical Devices recalls

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

Total recalls
40,372
Top agency
FDA Devices
Years covered
2000–2026
Check a product → All categories

Medical Devices accounts for 40,372 recalls, about 39.7% of the federal recall archive, of which 9% of graded records are high-severity.

The FDA, CPSC and NHTSA have published 40,372 medical devices recalls between 2000 and 2026 - roughly 39.7% of the 101,704-record archive. Of the 40,372 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.

  • 40,372 total recalls
  • 39.7% of the archive
  • 9% graded high-severity
  • FDA Devices top agency

Category snapshot

Medical Devices accounts for 40,372 recalls, about 39.7% of the 101,704-record federal archive, with 3,538 graded high-severity, most issued by FDA Devices.

40,372
total recalls
9%
graded high-severity
FDA Devices
top issuing agency
2000–2026
years covered

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 1248

Source: FDA · CPSC · NHTSA As of Jul 2, 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 89 of 808

FDA Devices Moderate Dec 4, 2024

SIGNA Architect, Nuclear Magnetic Resonance Imaging System

GE Medical Systems, LLC

FDA Devices Moderate Dec 4, 2024

MEDLINE procedure kits labeled as follows: 1) PERIPHERAL CONTINUOUS NERVE BL, REF PAIN1423A; 2) CONT. 20G EPI MRI COMPATIBLE, REF PAIN1470A; 3) E…

MEDLINE INDUSTRIES, LP - Northfield

FDA Devices Moderate Dec 4, 2024

Baxter MiniCap Extended Life PD Transfer Set (long) with Titanium Spike, Part Number T5C4325K; use in Peritoneal Dialysis

Baxter Healthcare Corporation

FDA Devices Moderate Dec 4, 2024

Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, Part Number R5C4482E; use in Peritoneal Dialysis

Baxter Healthcare Corporation

FDA Devices Moderate Dec 4, 2024

Defibtech DDP-200P: Pediatric Defibrillation Pads 0 For use with AED Models: Lifeline and Lifeline Auto (DDU-l XX Series)-Indicated for use on victi…

Defibtech, LLC

FDA Devices Moderate Dec 4, 2024

Defibtech DDP-100 Adult Defibrillation Pads For use with AED Models: Lifeline and Lifeline Auto (DDU-1:XX Series)- Indicated for use on victims of s…

Defibtech, LLC

FDA Devices Moderate Dec 4, 2024

MEDLINE procedure kits labeled as follows: 1) L&D CONTINUOUS EPIDURAL TRAY, REF PAIN1699; 2) L&D CONTINUOUS EPIDURAL TRAY, REF PAIN1699A

MEDLINE INDUSTRIES, LP - Northfield

FDA Devices Moderate Dec 4, 2024

SENSE Breast Coil 3.0T 7ch

Philips North America Llc

FDA Devices Moderate Dec 4, 2024

Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, Part Number 5C4482S; use in Peritoneal Dialysis

Baxter Healthcare Corporation

FDA Devices Moderate Dec 4, 2024

4.5 x 180 mm REF 28208BKS Aggressive Cutter, sterile, 6x 3.5 x 70 mm REF 28206CBS Full Radius Resector, sterile, 6x 5.5 x 120 mm REF 28205NDS A…

Karl Storz Endoscopy

FDA Devices Moderate Dec 4, 2024

VITROS Chemistry Products CRP Slides- In vitro diagnostic quantitatively measures C-reactive protein (CRP) concentration in serum and plasma Model/C…

Ortho-Clinical Diagnostics, Inc.

FDA Devices Moderate Dec 4, 2024

Defibtech DDP-2002: Pediatric Defibrillation Pads For use with AED Models: Lifeline View Auto, lifeline Pro, Lifeline ECG, Lifeline View (DDU-2XXX S…

Defibtech, LLC

FDA Devices Moderate Dec 4, 2024

Kreatech PapV-16, Flu labeled ISH probe, to detect presence of HPV-16 DNA inserts in human tissue, Model Number 40V016V495

Kreatech Biotechnology Bv

FDA Devices Moderate Dec 4, 2024

Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, Part Number R5C4483; use in Peritoneal Dialysis

Baxter Healthcare Corporation

FDA Devices Moderate Dec 4, 2024

dS Breast 7ch 1.5T

Philips North America Llc

FDA Devices Moderate Dec 4, 2024

Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, Part Number R5C4482; use in Peritoneal Dialysis

Baxter Healthcare Corporation

FDA Devices Moderate Dec 4, 2024

Tomographic Imager Combining Emission Computed Tomography With Nuclear Magnetic Resonance: 1) SIGNA PET/MR, 2) DISCOVERY PET/MR,

GE Medical Systems, LLC

FDA Devices Moderate Dec 4, 2024

Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, Part Number R5C4484; use in Peritoneal Dialysis

Baxter Healthcare Corporation

FDA Devices Moderate Dec 4, 2024

Autosampler, Models: SIL-20ACXR CL, SIL-20ACHT CL, SIL-30AC CL

Shimadzu Corp. Analytical & Measuring Instruments Div.

FDA Devices Moderate Dec 4, 2024

ENDO KIT, Medline Kit SKU DYKE1577A, Component Number 57469, 10 per case; Medline Convenience Kits containing Single Use Biopsy Valve MAJ-1555

MEDLINE INDUSTRIES, LP - Northfield

FDA Devices Moderate Dec 4, 2024

Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, Part Number T5C4482; use in Peritoneal Dialysis

Baxter Healthcare Corporation

FDA Devices Moderate Dec 4, 2024

Offset Cup Impactor - 3/8-16 interface. Reusable surgical instrument used to position and place acetabular sup implants.

INCIPIO DEVICES

FDA Devices Low Dec 4, 2024

Merlin@home with the MerlinOnDemand capability Transmitter REF EX1150 Merlin@home with the MerlinOnDemand" (MoD) capability is a transmitter conf…

Abbott Medical

FDA Devices Low Dec 4, 2024

Tempus LS-Manual Defibrillator Model 00-3020 The Tempus LS-Manual is a defibrillator that can deliver a shock in manual or Pacemaker mode

Remote Diagnostic Technologies Ltd.

FDA Devices Moderate Dec 4, 2024

dS Breast 16ch 3.0T

Philips North America Llc

FDA Devices Moderate Dec 4, 2024

ST SENSE Breast Coil

Philips North America Llc

FDA Devices Moderate Dec 4, 2024

Mammotrak Interventional Coil 1.5T

Philips North America Llc

FDA Devices Moderate Dec 4, 2024

MEDLINE procedure kits labeled as follows: 1) NEURAXIAL KIT, REF PAIN1876A

MEDLINE INDUSTRIES, LP - Northfield

FDA Devices Moderate Dec 4, 2024

MEDLINE NEXUS 19/20G CATH CONNECTOR, Medline SKU REF NEXCONNECT, Catheter Connector

MEDLINE INDUSTRIES, LP - Northfield

FDA Devices Moderate Dec 4, 2024

Essenz HLM (Heart-Lung Machine), REF: 49-00-10, with Software

LivaNova Deutschland GmbH

FDA Devices Moderate Dec 4, 2024

Mammotrak Diagnostic Coil 3.0T

Philips North America Llc

FDA Devices Moderate Dec 4, 2024

Achieva TX Interventional Coil 3.0T

Philips North America Llc

FDA Devices Moderate Nov 27, 2024

EnChroma Safety Glasses with Rx Indoor Universal Lenses: Martinez Cx1 Indoor Rx, SKU: Cx.PC.IN.MTZ.BK.Rx; Summit Indoor Rx, Cx.PC.IN.SUM.BK.Rx; Ma…

Enchroma Inc

FDA Devices Moderate Nov 27, 2024

Acrobat-i Vacuum Stabilizer System. Model Number C-OM-10000Z

Maquet Cardiovascular, LLC

FDA Devices Moderate Nov 27, 2024

Posi-Stop Injection Needle, 25 Gauge, Catalog Number: 4723

Hobbs Medical, Inc.

FDA Devices Critical Nov 27, 2024

Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, Part Number 5C4482; use in Peritoneal Dialysis

Baxter Healthcare Corporation

FDA Devices Moderate Nov 27, 2024

CAIRE FreeStyle Comfort portable oxygen concentrator, model #AS200-2.

Caire, Inc.

FDA Devices Moderate Nov 27, 2024

Posi-Stop Injection Needle, 25 Gauge, Catalog Number: 4722

Hobbs Medical, Inc.

FDA Devices Critical Nov 27, 2024

Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, Part Number 5C4482S; use in Peritoneal Dialysis

Baxter Healthcare Corporation

FDA Devices Moderate Nov 27, 2024

Precice Max REF: PM10.0-80B265 PRECICE MAX Antegrade Femur Piriformis Straight 10.0mm x 265mm PM10.0-80B280 PRECICE MAX Antegrade Femur Piriform…

NuVasive Specialized Orthopedics, Inc.

FDA Devices Moderate Nov 27, 2024

Abbott Navitor Transcatheter Aortic Heart Valve, 27 mm, NVTR-27, Sterile

Abbott Medical

FDA Devices Moderate Nov 27, 2024

Abbott Navitor Transcatheter Aortic Heart Valve, 29 mm, NVTR-29, Sterile

Abbott Medical

FDA Devices Moderate Nov 27, 2024

Posi-Stop Injection Needle, 23 Gauge, Catalog Number: 4721

Hobbs Medical, Inc.

FDA Devices Moderate Nov 27, 2024

Z-800 Infusion System. Model/Catalog Number: Z-800, Z-800F, Z-800W, Z-800WF. The Z-800 Infusion system is intended to provide intravenous infusi…

Zyno Medical LLC

FDA Devices Moderate Nov 27, 2024

cobas HCYS, Homocysteine Enzymatic Assay, Material Number REF 06542921190, for use on cobas c 701/702, in vitro test for total L-homocysteine

Roche Diagnostics Operations, Inc.

FDA Devices Moderate Nov 27, 2024

Abbott Navitor Titan, Vision Technology, Transcatheter Aortic Heart Valve, 35 mm, NVRO-35, Sterile

Abbott Medical

FDA Devices Critical Nov 27, 2024

Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, Part Number R5C4482; use in Peritoneal Dialysis

Baxter Healthcare Corporation

FDA Devices Moderate Nov 27, 2024

Abbott Navitor, Vision Technology, Transcatheter Aortic Heart Valve, 27 mm, NVRO-27, Sterile

Abbott Medical

FDA Devices Moderate Nov 27, 2024

Posi-Stop Injection Needle, 25 Gauge, Catalog Number: 4718

Hobbs Medical, Inc.

FDA Devices Moderate Nov 27, 2024

Posi-Stop Injection Needle, 23 Gauge, Catalog Number: 4716

Hobbs Medical, 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 2, 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 2, 2026.