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

Where Medical Devices sits among all 12 categories

Distinct recall-event inventory across every PlainRecalls product category. Medical Devices is marked; archive size reflects reporting volume, not inherent product danger.

Medical Devices vs all categories by recall count

Where this category's archive sits among every tracked product class

40,910 1st of 12 the highest of 12 categories

Categories, banded by distinct recall-event inventory

Each bar is a band; taller bars hold more categories. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source FDA · CPSC · NHTSA federal recall filings · 2026-08-25

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 540 of 819

FDA Devices Moderate May 10, 2017

19cm Attachment, Black Max Product Usage: Pneumatic system

The Anspach Effort, Inc.

FDA Devices Moderate May 10, 2017

Autolube-III with Foot Guard Product Usage: Pneumatic system

The Anspach Effort, Inc.

FDA Devices Moderate May 10, 2017

11.0cm Long Attachment Product Usage: Pneumatic system

The Anspach Effort, Inc.

FDA Devices Moderate May 10, 2017

Autolube-III with Irrigation Product Usage: Pneumatic system

The Anspach Effort, Inc.

FDA Devices Moderate May 10, 2017

5.0cm Short Attachment

The Anspach Effort, Inc.

FDA Devices Moderate May 10, 2017

Large Craniotome Product Usage: Pneumatic system

The Anspach Effort, Inc.

FDA Devices Moderate May 10, 2017

8cm QD Angle Attachment

The Anspach Effort, Inc.

FDA Devices Moderate May 10, 2017

Dressing M/U XL, P/N 02344 Product Usage: These products are sterile dressings used as an insulation barrier between the Polar Care cold therapy …

Breg Inc

FDA Devices Moderate May 10, 2017

13.5CM ANGLE ATTACHMENT, BLACK MAX

The Anspach Effort, Inc.

FDA Devices Moderate May 10, 2017

26.65CM ATTACHMENT, BLACK MAX

The Anspach Effort, Inc.

FDA Devices Moderate May 10, 2017

Bearing Sleeve, 10CM Straight Product Usage: Pneumatic system

The Anspach Effort, Inc.

FDA Devices Moderate May 10, 2017

Autolube-III with 20ft hose Product Usage: Pneumatic system

The Anspach Effort, Inc.

FDA Devices Moderate May 10, 2017

eMax2 PLUS Product Usage: Electric system

The Anspach Effort, Inc.

FDA Devices Moderate May 10, 2017

Reciprocating MICRO SAW

The Anspach Effort, Inc.

FDA Devices Moderate May 10, 2017

Second generation neoBLUE LED Phototherapy Light (neoBLUE 2) sold between 2003 and 2008. Catalog Part Number 010066. Top Assembly Part Numbers: 0409…

Natus Medical Incorporated

FDA Devices Moderate May 10, 2017

Electronic Foot Control with Direction or Irrigation Switches Product Usage: Electric system

The Anspach Effort, Inc.

FDA Devices Moderate May 10, 2017

Compact Speed Reducer, 60:1

The Anspach Effort, Inc.

FDA Devices Moderate May 10, 2017

Dressing, Knee L/XL, P/N 04708 Product Usage: These products are sterile dressings used as an insulation barrier between the Polar Care cold ther…

Breg Inc

FDA Devices Moderate May 10, 2017

6.1CM ATTACHMENT, BLACK MAX Product Usage: Pneumatic system

The Anspach Effort, Inc.

FDA Devices Moderate May 10, 2017

7.5cm QD Angle Attachment

The Anspach Effort, Inc.

FDA Devices Moderate May 10, 2017

10.5cm Long Attachment, Non-Tapered End Product Usage: Pneumatic system

The Anspach Effort, Inc.

FDA Devices Moderate May 10, 2017

Destination Renal Guiding Sheath Intended for the introduction of interventional and diagnostic devices into the human vasculature.

Terumo Medical Corporation

FDA Devices Moderate May 10, 2017

10.5cm Long Attachment Product Usage: Pneumatic system

The Anspach Effort, Inc.

FDA Devices Moderate May 10, 2017

9.4CM MICRO REVISION ATTACH, BLACK MAX

The Anspach Effort, Inc.

FDA Devices Moderate May 10, 2017

CONTRA ANGLE ATTACHMENT, BLACK MAX

The Anspach Effort, Inc.

FDA Devices Moderate May 10, 2017

ADJUSTABLE DRILL GUIDE, BLACK MAX

The Anspach Effort, Inc.

FDA Devices Moderate May 10, 2017

Bearing Sleeve, 19CM Straight Taper Product Usage: Pneumatic system

The Anspach Effort, Inc.

FDA Devices Moderate May 10, 2017

8.0CM Heavy Duty Medium Attachment Product Usage: Pneumatic system

The Anspach Effort, Inc.

FDA Devices Moderate May 10, 2017

Dressing Back, P/N 09810 Product Usage: These products are sterile dressings used as an insulation barrier between the Polar Care cold therapy pa…

Breg Inc

FDA Devices Moderate May 10, 2017

Sonesta S2; Article numbers: 525-S2-110V and 525¿¿S2-220V

Sonesta Medical Ab

FDA Devices Moderate May 10, 2017

GREEN ROTATING CRANIOTOME, BLACK MAX

The Anspach Effort, Inc.

FDA Devices Moderate May 10, 2017

7.5CM ANGLE ATTACHMENT, BLACK MAX

The Anspach Effort, Inc.

FDA Devices Moderate May 10, 2017

SurFlo IV Catheter

Terumo Medical Corporation

FDA Devices Moderate May 10, 2017

14CM ANGLE ATTACHMENT, BLACK MAX

The Anspach Effort, Inc.

FDA Devices Moderate May 10, 2017

Dressing Knee/Shldr, P/N 02328 Product Usage: These products are sterile dressings used as an insulation barrier between the Polar Care cold ther…

Breg Inc

FDA Devices Moderate May 10, 2017

System Console, Single Port, no irrigation

The Anspach Effort, Inc.

FDA Devices Moderate May 10, 2017

12.4cm Heavy Duty Long Heavy Short Attachment Product Usage: Pneumatic system

The Anspach Effort, Inc.

FDA Devices Moderate May 10, 2017

RENOVATION, RADIAL OSTEOTOME BLADE, SIZE 16, REF 71369316, STERILE R, QTY: (1)

Smith & Nephew, Inc.

FDA Devices Moderate May 10, 2017

45 degree Contra Angle Attachment Product Usage: Pneumatic system

The Anspach Effort, Inc.

FDA Devices Moderate May 10, 2017

90 DEG RIGHT ANGLE ATTACH, BLACK MAX

The Anspach Effort, Inc.

FDA Devices Moderate May 10, 2017

Bearing Sleeve, 15CM Curved Product Usage: Pneumatic system

The Anspach Effort, Inc.

FDA Devices Moderate May 10, 2017

The JETSTREAM is a rotational atherectomy catheter system designed for use in debulking and treating vascular disease in the peripheral vasculature. …

Boston Scientific Corporation

FDA Devices Moderate May 10, 2017

IMRI CRANI-A ATTACHMENT Product Usage: Pneumatic system

The Anspach Effort, Inc.

FDA Devices Moderate May 10, 2017

RENOVATION, RADIAL OSTEOTOME BLADE, SIZE 10, REF 71369310, STERILE R, QTY: (1)

Smith & Nephew, Inc.

FDA Devices Moderate May 10, 2017

eMax2 Motor Assembly Product Usage: Electric system

The Anspach Effort, Inc.

FDA Devices Moderate May 10, 2017

16CM MIN INVASIVE ATTACH, BLACK MAX

The Anspach Effort, Inc.

FDA Devices Moderate May 10, 2017

AL-III-DISS Adapter Product Usage: Pneumatic system

The Anspach Effort, Inc.

FDA Devices Moderate May 10, 2017

Dressing Shldr, P/N 04908 Product Usage: These products are sterile dressings used as an insulation barrier between the Polar Care cold therapy p…

Breg Inc

FDA Devices Moderate May 10, 2017

DOLPHIN INFLATION DEVICE CALIBER INFLATION DEVICE; Catalog Number: CL3030- 018SNA- 018SND 0185NA 0185ND; INTERNAL CODE NUMBER: 0185TR- 0185NA- 018SND…

PEROUSE MEDICAL

FDA Devices Moderate May 10, 2017

11CM ANGLE ATTACHMENT, BLACK MAX

The Anspach Effort, 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.