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 533 of 819

FDA Devices Moderate Jun 21, 2017

VITEK¿ 2 Gram Negative Susceptibility card (AST-N238), REF 413203, 20 cards per carton.

Biomerieux Inc

FDA Devices Moderate Jun 21, 2017

VITEK¿ 2 Gram Negative Susceptibility card (AST-N204), REF 412865, 20 cards per carton. .

Biomerieux Inc

FDA Devices Moderate Jun 21, 2017

VITEK¿ 2 Gram Negative Susceptibility card (AST-GN81), REF 413438, 20 cards per carton.

Biomerieux Inc

FDA Devices Moderate Jun 21, 2017

ARROWg+ard Blue CVC Kit The ARROWg+ard Blue CVCs are intended to permit venous access to the central circulation

Arrow International Inc

FDA Devices Moderate Jun 21, 2017

VITEK¿ 2 Gram Negative Susceptibility card (AST-N209), REF 412938, 20 cards per carton.

Biomerieux Inc

FDA Devices Moderate Jun 21, 2017

VITEK¿ 2 Gram Negative Susceptibility card (AST-GN87), REF 413943, 20 cards per carton.

Biomerieux Inc

FDA Devices Moderate Jun 21, 2017

VITEK¿ 2 Gram Negative Susceptibility card (AST-N233), REF 413117, 20 cards per carton.

Biomerieux Inc

FDA Devices Moderate Jun 21, 2017

VITEK¿ 2 Gram Negative Susceptibility card (AST-N320), IVD, REF 418204, 20 cards per carton.

Biomerieux Inc

FDA Devices Moderate Jun 21, 2017

VITEK¿ 2 Gram Negative Susceptibility card (AST-N352), IVD, REF 421258, 20 cards per carton.

Biomerieux Inc

FDA Devices Moderate Jun 21, 2017

Segmental vss bowed 19x190mm, Sterile, Hip joint, metal/ceramic/polymer, semi-constrained, cemented or nonporous uncemented prosthesis- Specific Kn…

Zimmer Biomet, Inc.

FDA Devices Moderate Jun 21, 2017

VITEK¿ 2 Gram Positive Susceptibility card (AST-P640), IVD, REF 418579, 20 cards per carton.

Biomerieux Inc

FDA Devices Moderate Jun 21, 2017

Fem IM Nail 16mmdx50cm, Sterile, Rod, fixation, intramedullary and accessories- Specific Knee, Hip and Nail Implants

Zimmer Biomet, Inc.

FDA Devices Moderate Jun 21, 2017

Segmental fluted stem, 17x250mm bwd, Sterile, Knee joint femorotibial meta/polymer constrained cemented prosthesis- Specific Knee, Hip and Nail Imp…

Zimmer Biomet, Inc.

FDA Devices Moderate Jun 21, 2017

VITEK¿ 2 Streptococcus Susceptibility card (AST-ST03), IVD, REF 421040, 20 cards per carton.

Biomerieux Inc

FDA Devices Moderate Jun 21, 2017

VITEK¿ 2 Gram Negative Susceptibility card (AST-N324), IVD, REF 418603, 20 cards per carton.

Biomerieux Inc

FDA Devices Moderate Jun 21, 2017

VITEK¿ 2 Gram Negative Susceptibility card (AST-N272), REF 414164, 20 cards per carton.

Biomerieux Inc

FDA Devices Moderate Jun 21, 2017

Fem IM Nail 16mmdx48cm, Sterile, Rod, fixation, intramedullary and accessories- Specific Knee, Hip and Nail Implants

Zimmer Biomet, Inc.

FDA Devices Moderate Jun 21, 2017

VITEK¿ 2 Gram Negative Susceptibility card (AST-N354), IVD, REF 421350, 20 cards per carton.

Biomerieux Inc

FDA Devices Moderate Jun 21, 2017

Boston Scientific Zurpaz(TM) MEDIUM CURL, SYMMETRIC CURVE, Steerable Sheath, 8.5F (2.83mm), REF Catalog No M004USMC85100

Creganna Medical Devices

FDA Devices Moderate Jun 21, 2017

VITEK¿ 2 Gram Negative Susceptibility card (AST-GN04), IVD, REF 22000, 20 cards per carton.

Biomerieux Inc

FDA Devices Moderate Jun 21, 2017

Por fullct fem st 16x200mm, Sterile,

Zimmer Biomet, Inc.

FDA Devices Moderate Jun 21, 2017

VITEK¿ 2 Gram Negative Susceptibility card (AST-N286), REF 414778, 20 cards per carton.

Biomerieux Inc

FDA Devices Moderate Jun 21, 2017

Monica Novii Wireless Patch System product Usage: Novii Interface - The Novii Interface is an accessory to the Novii Pod which provides a means o…

MONICA HEALTHCARE LTD

FDA Devices Moderate Jun 21, 2017

VITEK¿ 2 Gram Negative Susceptibility card (AST-N363), IVD, REF 421692, 20 cards per carton.

Biomerieux Inc

FDA Devices Moderate Jun 21, 2017

Boston Scientific Zurpaz(TM) MEDIUM CURL, ASYMMETRIC CURVE, Steerable Sheath, 8.5F (2.83mm), REF Catalog No M004USTMCA85200

Creganna Medical Devices

FDA Devices Moderate Jun 21, 2017

Fem IM Nail 14mmdx48cm right, Sterile, Rod, fixation, intramedullary and accessories- Specific Knee, Hip and Nail Implants

Zimmer Biomet, Inc.

FDA Devices Moderate Jun 21, 2017

Video Naso pharyngo Laryngoscopes

Pentax of America Inc

FDA Devices Moderate Jun 21, 2017

Kii Shielded Bladed trocars (CTB14), Kii Low profile trocars (CTB23), and Kii 5x55mm Optical Z-Thread Dual Pack (CTR14) trocars.

Applied Medical Resources Corp

FDA Devices Moderate Jun 21, 2017

R-F IM NAIL 10MMDX48CM LG, 11MMDX42CM, 11MMDX44CM, 11MMDX46CM LG, 11MMDX48CM LG, 12MMDX46CM LG, 12MMDX48CM LG, 13MMDX40CM, 13MMDX42CM, 13MMDX44CM, …

Zimmer Biomet, Inc.

FDA Devices Moderate Jun 21, 2017

VITEK¿ 2 Gram Negative Susceptibility card (AST-GN82), REF 413439, 20 cards per carton.

Biomerieux Inc

FDA Devices Moderate Jun 21, 2017

VITEK¿ 2 Gram Negative Susceptibility card (AST-N315), IVD, REF 417426, 20 cards per carton.

Biomerieux Inc

FDA Devices Moderate Jun 21, 2017

GE Healthcare Revolution EVO X-ray system

GE Healthcare, LLC

FDA Devices Moderate Jun 21, 2017

VITEK¿ 2 Gram Negative Susceptibility card (AST-N285), REF 414740, 20 cards per carton.

Biomerieux Inc

FDA Devices Moderate Jun 21, 2017

VITEK¿ 2 Gram Positive Susceptibility card (AST-P644), IVD, REF 418673, 20 cards per carton.

Biomerieux Inc

FDA Devices Moderate Jun 21, 2017

GE Healthcare Discovery PET/CT 600,610, 690, 710: Optima PET/CT 560. 560FX X-ray system

GE Healthcare, LLC

FDA Devices Moderate Jun 21, 2017

VITEK¿ 2 Gram Positive Susceptibility card (AST-P621), REF 412533, 20 cards per carton.

Biomerieux Inc

FDA Devices Moderate Jun 21, 2017

Tibial IM Nail 15mmdx44cm, Sterile, Rod, fixation, intramedullary and accessories- Specific Knee, Hip and Nail Implants

Zimmer Biomet, Inc.

FDA Devices Moderate Jun 21, 2017

VITEK¿ 2 Gram Positive Susceptibility card (AST-GP71), REF 410750, 20 cards per carton.

Biomerieux Inc

FDA Devices Moderate Jun 21, 2017

Merge PACS software. The firm name on the label is Merge Healthcare, Hartland, WI.

Merge Healthcare, Inc.

FDA Devices Moderate Jun 21, 2017

VITEK¿ 2 Gram Negative Susceptibility card (AST-N217), REF 413080, 20 cards per carton.

Biomerieux Inc

FDA Devices Moderate Jun 21, 2017

VITEK¿ 2 Gram Negative Susceptibility card (AST-N292), REF 415063, 20 cards per carton.

Biomerieux Inc

FDA Devices Moderate Jun 21, 2017

VITEK¿ 2 Gram Positive Susceptibility card (AST-P606), REF 22330, 20 cards per carton.

Biomerieux Inc

FDA Devices Moderate Jun 21, 2017

VITEK¿ 2 Gram Positive Susceptibility card (AST-P629), REF 414576, 20 cards per carton.

Biomerieux Inc

FDA Devices Moderate Jun 21, 2017

Pereyra Ligature Carrier 75

Cook Inc.

FDA Devices Moderate Jun 21, 2017

VITEK¿ 2 Gram Negative Susceptibility card (AST-N350), IVD, REF 421037, 20 cards per carton.

Biomerieux Inc

FDA Devices Moderate Jun 21, 2017

VITEK¿ 2 Gram Positive Susceptibility card (AST-P603), REF 22320, 20 cards per carton.

Biomerieux Inc

FDA Devices Moderate Jun 21, 2017

VITEK¿ 2 Gram Negative Susceptibility card (AST-N211), REF 413043, 20 cards per carton.

Biomerieux Inc

FDA Devices Moderate Jun 21, 2017

Segmental fluted stem, 18x250mm bwd, Sterile,

Zimmer Biomet, Inc.

FDA Devices Moderate Jun 21, 2017

VITEK¿ 2 Gram Negative Susceptibility card (AST-N293), REF 415369, 20 cards per carton.

Biomerieux Inc

FDA Devices Moderate Jun 14, 2017

Arrow Pressure Injectable PICC Kit The Arrow International Pressure Injectable PICC is intended for short-term or long-term peripheral access to the…

Arrow International 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.