PlainRecalls

Product category · Updated Jun 3, 2026

Medical Devices recalls

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

Total recalls
40,478
Top agency
FDA Devices
Years covered
2000–2026
Check a product → All categories

Medical Devices accounts for 40,478 recalls — about 40.4% of the federal recall archive, of which 9% of graded records are high-severity.

The FDA, CPSC and NHTSA have published 40,478 medical devices recalls between 2000 and 2026 — roughly 40.4% of the 100,165-record archive. Of the 40,478 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.

  • 40,478 total recalls
  • 40.4% of the archive
  • 9% graded high-severity
  • FDA Devices top agency

Category snapshot

Medical Devices accounts for 40,478 recalls — about 40.4% of the 100,165-record federal archive, with 3,549 graded high-severity, most issued by FDA Devices.

40,478
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 2567 3385 2655 3821 3004 3208 2360 2254 2607 3417 2992 1243

Source: FDA · CPSC · NHTSA As of Jun 3, 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 50 of 810

FDA Devices Low Sep 3, 2025

SCNHD LA L7-4 HDI Transducer Probe

Philips Ultrasound, Inc

FDA Devices Low Sep 3, 2025

L8-4 Transducer Probe

Philips Ultrasound, Inc

FDA Devices Low Sep 3, 2025

7.5MHZ Endo Transducer Probe

Philips Ultrasound, Inc

FDA Devices Moderate Sep 3, 2025

Orascoptic Superior Visualization Phantom Nose Pad Accessory Kit ( nose pad and screw) 1 pk. and 20 pk.

Orascoptic Surgical Acuity

FDA Devices Low Sep 3, 2025

L10-4LAP Transducer Probe

Philips Ultrasound, Inc

FDA Devices Low Sep 3, 2025

C10-4ec Transducer Probe

Philips Ultrasound, Inc

FDA Devices Moderate Sep 3, 2025

Brand Name: THOR Product Name: NovoTHOR Gen 3.0 Reg PRX Model/Catalog Number: S2186 Software Version: N/A Product Description: The NovoTHOR and N…

THOR Photomedicine Ltd

FDA Devices Low Sep 3, 2025

X5-1 Transducer Probe

Philips Ultrasound, Inc

FDA Devices Moderate Sep 3, 2025

PrisMax V2-US, Hemodialysis Delivery System, Product Codes: 955626, 955558, 955627, 955701

VANTIVE US HEALTHCARE LLC

FDA Devices Moderate Sep 3, 2025

AMERICAN CONTRACT SYSTEMS, Medical Procedure kits and trays labeled as: 1) SFCH CRANI PACK (PS 132432), MODEL/ITEM NUMBER UICR10W; 2) SFCH SHUNT…

American Contract Systems Inc

FDA Devices Low Sep 3, 2025

C8-4v Transducer Probe

Philips Ultrasound, Inc

FDA Devices Low Sep 3, 2025

VL13-5 Transducer Probe

Philips Ultrasound, Inc

FDA Devices Low Sep 3, 2025

S4-1 Lumify Transducer Probe

Philips Ultrasound, Inc

FDA Devices Low Sep 3, 2025

S4-2 Transducer Probe

Philips Ultrasound, Inc

FDA Devices Low Sep 3, 2025

OMNI II TEE Transducer Probe

Philips Ultrasound, Inc

FDA Devices Low Sep 3, 2025

C9-2 Transducer Probe

Philips Ultrasound, Inc

FDA Devices Low Sep 3, 2025

Akreos, SKU: AO60P0300. Akreos intraocular lenses

Bausch & Lomb Surgical, Inc.

FDA Devices Low Sep 3, 2025

3D9-3v Transducer Probe

Philips Ultrasound, Inc

FDA Devices Low Sep 3, 2025

L18-5 Transducer Probe

Philips Ultrasound, Inc

FDA Devices Moderate Sep 3, 2025

Brand Name: Atlantis IO FLO Product Name: Atlantis IO FLO-S Kit Model/Catalog Number: A04S / 6802034 Product Description: The Atlantis intraoral f…

Dentsply IH, Inc.

FDA Devices Moderate Sep 3, 2025

STA-Liquid Anti-Xa 4. Model/Catalog Number: 00311US. The STA - Liquid Anti-Xa kits are intended for use with STA-R, STA Compact and STA Satellite …

Diagnostica Stago, Inc.

FDA Devices Moderate Sep 3, 2025

AMERICAN CONTRACT SYSTEMS, Medical Procedure kits and trays labeled as: 1) HEART PACK - 205947, MODEL/ITEM NUMBER ANCV78BC; 2) VASCULAR PACK - 2…

American Contract Systems Inc

FDA Devices Low Sep 3, 2025

D2cwc Transducer Probe

Philips Ultrasound, Inc

FDA Devices Moderate Sep 3, 2025

Orascoptic Superior Visualization Dragonfly Nose Pad Accessory Kit ( nose pad and screw) 1 pk and 20 pk.

Orascoptic Surgical Acuity

FDA Devices Low Sep 3, 2025

mL26-8 Transducer Probe

Philips Ultrasound, Inc

FDA Devices Moderate Sep 3, 2025

AMERICAN CONTRACT SYSTEMS, Medical Procedure kits and trays labeled as: 1) A-C SUPPLEMENT PACK - 205946, Model/Item Number ANCV67X; 2) KIDNEY P…

American Contract Systems Inc

FDA Devices Low Sep 3, 2025

C6-3 Transducer Probe

Philips Ultrasound, Inc

FDA Devices Low Sep 3, 2025

eL18-4 Transducer Probe

Philips Ultrasound, Inc

FDA Devices Moderate Sep 3, 2025

STA Satellite. Product Code: All references. All software versions. The STA Satellite is a fully automated benchtop analyzer capable of simultaneo…

Diagnostica Stago, Inc.

FDA Devices Low Sep 3, 2025

mC12-3 Transducer Probe

Philips Ultrasound, Inc

FDA Devices Moderate Sep 3, 2025

TherMax Blood Warmer Unit-US, PrisMax Accessory, Product Codes: 955630, 955515, 955702, 955631

VANTIVE US HEALTHCARE LLC

FDA Devices Low Sep 3, 2025

L15-7io Transducer Probe

Philips Ultrasound, Inc

FDA Devices Low Sep 3, 2025

X5-1c Transducer Probe

Philips Ultrasound, Inc

FDA Devices Low Sep 3, 2025

L12-4 Lumify Transducer Probe

Philips Ultrasound, Inc

FDA Devices Low Sep 3, 2025

S7-3t Transducer Probe

Philips Ultrasound, Inc

FDA Devices Moderate Sep 3, 2025

Brand Name: Atlantis IO FLO-S Product Name: Atlantis IO FLO-S Kit Model/Catalog Number: A04B / 68020033 Software Version: n/a Product Description…

Dentsply IH, Inc.

FDA Devices Low Sep 3, 2025

S5-2 Transducer Probe

Philips Ultrasound, Inc

FDA Devices Low Sep 3, 2025

3D6-2 Transducer Probe

Philips Ultrasound, Inc

FDA Devices Low Sep 3, 2025

C9-4v Transducer Probe

Philips Ultrasound, Inc

FDA Devices Low Sep 3, 2025

S3-1 Transducer Probe

Philips Ultrasound, Inc

FDA Devices Low Sep 3, 2025

S8-3t Transducer Probe

Philips Ultrasound, Inc

FDA Devices Low Sep 3, 2025

D5cwc Transducer Probe

Philips Ultrasound, Inc

FDA Devices Low Sep 3, 2025

Transducer C10-3v Transducer Probe

Philips Ultrasound, Inc

FDA Devices Low Sep 3, 2025

X11-4t Transducer Probe

Philips Ultrasound, Inc

FDA Devices Moderate Sep 3, 2025

IPC Powerease System REF 2300000 UDI-DI: 00613994448705 00643169406834. The IPC POWEREASE System is indicated for drilling, tapping, and drivin…

Medtronic Xomed, Inc.

FDA Devices Low Sep 3, 2025

L12-3 Transducer Probe

Philips Ultrasound, Inc

FDA Devices Moderate Sep 3, 2025

STA-Liquid Anti-Xa 8. Model/Catalog Number: 00322US. The STA - Liquid Anti-Xa kits are intended for use with STA-R, STA Compact and STA Satellite…

Diagnostica Stago, Inc.

FDA Devices Moderate Sep 3, 2025

AMERICAN CONTRACT SYSTEMS, Medical Procedure kits and trays labeled as: 1) LAP CHOLE PACK, Model/Item Number CILC69L; 2) LAP CHOLE PACK, Model/I…

American Contract Systems Inc

FDA Devices Low Sep 3, 2025

Mini Multi TEE Transducer Probe

Philips Ultrasound, Inc

FDA Devices Moderate Sep 3, 2025

BD PhaSeal Injector Luer (N30C), REF: 515001 BD PhaSeal Injector Luer Lock (N35), REF: 515003 BD PhaSeal Injector Luer Lock (N35C), REF: 515004 BD…

BD SWITZERLAND SARL

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 Jun 3, 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 Jun 3, 2026.