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 12 of 808

FDA Devices Moderate Apr 8, 2026

MiniMed 780G Insulin Pump (MMT-1884, MMT-1885, MMT-1886, MMT-1894, MMT-1895, MMT-1896)

Medtronic MiniMed, Inc.

FDA Devices Moderate Apr 8, 2026

MiniMed 640G Insulin Pump (MMT-1711, MMT-1712, MMT-1751, MMT-1752)

Medtronic MiniMed, Inc.

FDA Devices Moderate Apr 8, 2026

Azurion 7 M12; System Code: (1)722078, (2)722223, (3)722233;

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

FDA Devices Moderate Apr 8, 2026

RefleXion X1 Radiotherapy System Model RXM1000, Part #800-00006-00

Reflexion Medical, Inc.

FDA Devices Moderate Apr 8, 2026

MiniMed 630G Insulin Pump (MMT-1714, MMT-1715, MMT-1754, MMT-1755)

Medtronic MiniMed, Inc.

FDA Devices Moderate Apr 8, 2026

CPX 4 US Breast Tissue Expanders with Suture Tabs Reference Numbers: SCPX-107MH, SCPX-117MH,SCPX-127MH, SCPX-135MH, SCPX-146MH, SCPX-156MH Smooth…

Mentor Texas, LP.

FDA Devices Critical Apr 8, 2026

Philips Respironics Trilogy Evo O2, Software Version 1.05.15.00. Continuous home-use ventilator device.

Philips Respironics, Inc.

FDA Devices Critical Apr 8, 2026

Philips Respironics Trilogy Evo Universal, Software Version 1.05.15.00. Continuous home-use ventilator device.

Philips Respironics, Inc.

FDA Devices Moderate Apr 8, 2026

Burlington Medical, Blockers.

Burlington Medical, LLC

FDA Devices Moderate Apr 8, 2026

Artoura Breast Tissue Expanders Reference Numbers: SDC-100UH SDC-110UH SDC-120UH SDC-130UH SDC-135UH SDC-140UH Smooth Ultra High Profile Tissue Exp…

Mentor Texas, LP.

FDA Devices Moderate Apr 8, 2026

Brand Name: da Vinci S, Si Monopolar Curved Scissors Instrument Product Name: da Vinci S and Si Monopolar Curved Scissors Instrument Model/Catalog …

Intuitive Surgical, Inc.

FDA Devices Moderate Apr 8, 2026

eTRAX Needle Sensor - 16G(for Aurora Trackers), Part Number 667-158

Civco Medical Instruments Co. Inc.

FDA Devices Moderate Apr 8, 2026

Azurion 5 M20; System Code: (1)722228, (2)722232, (3) 722281 (OUS only);

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

FDA Devices Critical Apr 8, 2026

Blue Ventilator Adapter Module, single-patient use circuit, Product Code M07937. Accessory to Baxter Volara Respiratory Therapy system.

Baxter Healthcare Corporation

FDA Devices Critical Apr 8, 2026

Philips Respironics Trilogy EV300, Software Version 1.05.15.00. Continuous home-use ventilator device.

Philips Respironics, Inc.

FDA Devices Moderate Apr 8, 2026

Allura Xper FD20/20 OR Table; System Code: 722039;

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

FDA Devices Moderate Apr 8, 2026

Medline convenience kits containing Olympus biopsy valves: 1. BRONCH PACK, DYKE2096 2. NON MB BRONCHOPSCOPY CCH LH PK, DYNJT6182 3. PULMONARY BR…

Medline Industries, LP

FDA Devices Moderate Apr 8, 2026

Brand Name: Olympus SOLTIVE Pro SuperPulsed Laser System Product Name: SOLTIVE Pro Laser System TFL-SLS Model/Catalog Number: TFL-SLS containing TF…

Olympus Corporation of the Americas

FDA Devices Moderate Apr 8, 2026

Brand Name: Finesse BTK Multicath Product Name: Injectable Angioplasty Balloon Catheter Model/Catalog Number: FS252251502 Product Description: 5 F…

SUMMA THERAPEUTICS, LLC

FDA Devices Moderate Apr 8, 2026

Sterile Radiology Procedure Kits, Model Number DYNDH1491B

Medline Industries, LP

FDA Devices Moderate Apr 8, 2026

Brand Name: da Vinci S, Si Double Fenestrated Grasper Instrument Product Name: da Vinci S, Si Double Fenestrated Grasper Instrument Model/Catalog N…

Intuitive Surgical, Inc.

FDA Devices Moderate Apr 8, 2026

MiniMed 770G Insulin Pump (MMT-1880, MMT-1881, MMT-1882, MMT-1890, MMT-1891, MMT-1892)

Medtronic MiniMed, Inc.

FDA Devices Moderate Apr 8, 2026

ALLURA Xper FD10/10; System Code: (1) 722005, (2)722011, (3)722027;

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

FDA Devices Moderate Apr 8, 2026

eTRAX Needle System Starter Kit 12G (for Aurora Trackers), Part Number 667-149

Civco Medical Instruments Co. Inc.

FDA Devices Moderate Apr 8, 2026

Burlington Medical, Thyroid Shield.

Burlington Medical, LLC

FDA Devices Moderate Apr 8, 2026

ALLURA Xper FD10 OR Table; System Code: (1) 722022, (2)722033;

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

FDA Devices Moderate Apr 8, 2026

Stryker CHROMOPHARE Softlit Ring Surgical Light System REF: CH00000001

Stryker Communications

FDA Devices Moderate Apr 8, 2026

Medline kits containing Olympus biopsy valves: 1. BAL KIT, DYNDA2137B 2. ENDO KIT, DYKE1915

Medline Industries, LP

FDA Devices Moderate Apr 8, 2026

Burlington Medical, Caps.

Burlington Medical, LLC

FDA Devices Critical Apr 8, 2026

Philips Respironics Trilogy Evo, Software Version 1.05.15.00. Continuous home-use ventilator device.

Philips Respironics, Inc.

FDA Devices Moderate Apr 8, 2026

Allura Xper FD20/15; System Code: 722058;

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

FDA Devices Moderate Apr 8, 2026

Allura Xper FD20/20; System Code: 722038;

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

FDA Devices Moderate Apr 8, 2026

Burlington Medical, Kilt

Burlington Medical, LLC

FDA Devices Moderate Apr 8, 2026

Brand Name: da Vinci S, Si Tenaculum Forceps Instrument Product Name: da Vinci S, Si Tenaculum Forceps Instrument Model/Catalog Number: 420207 Sof…

Intuitive Surgical, Inc.

FDA Devices Moderate Apr 8, 2026

Burlington Medical, BAT (Breast, Axilla and Thyroid) Coverage.

Burlington Medical, LLC

FDA Devices Moderate Apr 8, 2026

ALLURA Xper FD20; System Code: (1) 722006, (2)722012, (3)722028;

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

FDA Devices Moderate Apr 8, 2026

Azurion 7 M20; System Code: (1)722079, (2)722224, (3)722234, (4)722282 (OUS only);

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

FDA Devices Moderate Apr 8, 2026

Vue Motion V12. Product Number: 1017979.

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

FDA Devices Moderate Apr 8, 2026

Brand Name: Paradise¿ Ultrasound Renal Denervation System Product Name: Paradise ¿ Catheter Model/Catalog Number: PRDS-068-02 Product Description:…

ReCor Medical Inc.

FDA Devices Moderate Apr 8, 2026

MiniMed 700G Insulin Pump (MMT-1801, MMT-1805, MMT-1850, MMT-1851)

Medtronic MiniMed, Inc.

FDA Devices Moderate Apr 8, 2026

MEDLINE ANTERIOR HIP PACK DYNJ64672B

Medline Industries, LP

FDA Devices Moderate Apr 8, 2026

Allura Xper FD10C; System Code: 722001;

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

FDA Devices Moderate Apr 8, 2026

2.4 VOLT(TM) TAP CORTEX SCREW TO 90MM. Part Number: 03.424.126-US.

Synthes (USA) Products LLC

FDA Devices Moderate Apr 8, 2026

Azurion 7 B12; System Code: (1)722067, (2)722225, (3)722235;

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

FDA Devices Moderate Apr 8, 2026

MiniMed 670G Insulin Pump (MMT-1760, MMT-1761, MMT-1762, MMT-1780, MMT-1781, MMT-1782)

Medtronic MiniMed, Inc.

FDA Devices Moderate Apr 8, 2026

Cardinal Health Monoject Tuberculin Syringe, 1 mL Luer Lock, Catalog Number 1180100777

Cardinal Health 200, LLC

FDA Devices Moderate Apr 8, 2026

ALLURA Xper FD10; System Code: (1) 722003, (2)722010, (3)722026;

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

FDA Devices Moderate Apr 1, 2026

Drill Plate, Ortho Dev. Trimax - Pegged, PREF Size 1 -5 REF:402566 component Lantern Knee System

Orthalign, Inc

FDA Devices Moderate Apr 1, 2026

Drill Plate, Ortho Dev. Trimax - Pegged, PREF Size 6-7 REF:402567 component Lantern Knee System

Orthalign, Inc

FDA Devices Moderate Apr 1, 2026

HCS - Headless Compression Screw System, Headless Compression Screw, Cannulated; Article Numbers: 31207-10, 31207-12, 31207-14, 31207-16, 31207-18, 3…

I.T.S. GmbH

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.