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 145 of 808

FDA Devices Moderate Feb 21, 2024

Microbiologics Enteric Pathogens Control Panel (Inactivated Pellet), REF 8184.

Microbiologics Inc

FDA Devices Critical Feb 21, 2024

GE Healthcare Care Plus Hood Field Replacement Unit (FRU) kit, Part Numbers: 6600-0047-851, 6600-0033-850, 6600-0081-850, 6600-0961-500, 6600-0083-8…

Wipro GE Healthcare Private Ltd.

FDA Devices Moderate Feb 21, 2024

AFT (Allograft Filler Tube) Diverted Tube (3/4 Filled), Product Code 227005 (bone void filler)

Musculoskeletal Transplant Foundation, Inc.

FDA Devices Moderate Feb 21, 2024

HeartSine samaritan PAD (Public Access Defibrillator): Type/Catalog: SAM 350P/350-UNIT-US-10, 350-STR-US-10, 350-STR-UK-10; SAM 360P/360-STR-JA-10, 3…

HeartSine Technologies Ltd

FDA Devices Critical Feb 21, 2024

GE Healthcare Lullaby Incubator Model Hood FRU kit, Part Numbers: M1169566, M1160659, M1206259, M1206260, M1166836, M1166814

Wipro GE Healthcare Private Ltd.

FDA Devices Critical Feb 21, 2024

GE Healthcare neonatal incubator, models: a) Lullaby Incubator, b) Lullaby Incubator XP, c) Lullaby Incubator TR

Wipro GE Healthcare Private Ltd.

FDA Devices Moderate Feb 21, 2024

CombiDiagnost R90 1.0 (709030)

PHILIPS MEDICAL SYSTEMS

FDA Devices Moderate Feb 21, 2024

global Medium, Model Numbers LGGG-020 (20mL bottle), LGGG-050 (50mL bottle), LGGG-100 (100mL bottle). Intended use: Culture of human embryos from zyg…

CooperSurgical, Inc.

FDA Devices Moderate Feb 21, 2024

BIOFIRE Blood Culture Identification 2 (BCID2) Panel when used with: BD BACTEC Lytic Anaerobic medium BD BACTEC Peds Plus medium BD BACTEC Plus…

BioFire Diagnostics, LLC

CPSC Moderate Feb 15, 2024

BRS and BULin Liquid Fuel Bottles Recalled Due to Risk of Poisoning, Burn, and Flash Fire; Violation of the Children's Gasoline Burn Prevention Safet…

WAOLi, of China

FDA Devices Moderate Feb 14, 2024

ExcelsiusGPS Cannula A, 9mm x 250mm, Cannula used with ball tip probes, Model No. 6143.2844

Globus Medical, Inc.

FDA Devices Moderate Feb 14, 2024

BD BBL Sensi Disc Piperacillin/Tazobactam- 100/10 ug, used for semi-quantitative in vitro susceptibility testing. Catalog Number 231691 and 231692¿

Becton Dickinson & Co.

FDA Devices Moderate Feb 14, 2024

BD BBL Sensi Disc Azithromycin -15 ¿g, Catalog Number 231682¿used for semi-quantitative in vitro susceptibility testing.

Becton Dickinson & Co.

FDA Devices Moderate Feb 14, 2024

BD BBL Sensi Disc Rifampin- 5 ug, used for semi-quantitative in vitro susceptibility testing. Catalog Number 231541 and 231544¿

Becton Dickinson & Co.

FDA Devices Moderate Feb 14, 2024

Access Ultrasensitive Insulin only used on the DxI 9000 Access Immunoassay Analyzer, Catalog Number 33410

Beckman Coulter, Inc.

FDA Devices Moderate Feb 14, 2024

Box as labeled: Regard, Carter-Thomason CloseSure System XL, REF 733776, Quantity 1 Box of 3 Systems. Kit as labeled: Regard, Carter-Thomason CloseS…

CooperSurgical, Inc.

FDA Devices Moderate Feb 14, 2024

BD BBL Sensi Disc Cefpodoxime - 10 ug, used for semi-quantitative in vitro susceptibility testing. Catalog Number 231673 and 231674¿

Becton Dickinson & Co.

FDA Devices Moderate Feb 14, 2024

FilmArray Pneumonia Panel Plus (Pneumoplus), REF: RFIT-ASY-0143, CED 2797, IVD, Rx Only (30 test kit)

BioFire Diagnostics, LLC

FDA Devices Moderate Feb 14, 2024

Olympus/Gyrus Paparrela-Type Vent Tube 1.02MM, Silicone, Sterile- to ventilate the middle ear subsequent to otitis media Model: 240044

Olympus Corporation of the Americas

FDA Devices Critical Feb 14, 2024

BrightView, gamma camera system; Model Nos.: 6-digit format 882480; 12-digit format 453560279781 453560279791 453560279811 453560279801; 4…

Philips North America

FDA Devices Moderate Feb 14, 2024

PulseSpray Infusion System devices including: PULSE SPRAY 5F/135/20, UPN: H787125004045, REF: 12500404; Pulse Spray 3Fx135x20, UPN: H787125004155, R…

Angiodynamics, Inc.

FDA Devices Moderate Feb 14, 2024

Sensi Disc Amoxicillin with Clavulanic Acid 20/10 ¿g, Catalog No. 231628 and 231629.¿ These discs are used for semi-quantitative in vitro suscepti…

Becton Dickinson & Co.

FDA Devices Moderate Feb 14, 2024

Water Filter MAJ-2318. This MAJ-2318 water filter has been designed to be used with Olympus endoscope reprocessor for prevent contamination of the ri…

Olympus Corporation of the Americas

FDA Devices Moderate Feb 14, 2024

Flow-c Anesthesia System, model 6887700

Getinge Usa Sales Inc

FDA Devices Critical Feb 14, 2024

Cardinal Health Monoject, 1 mL Purple Enteral Syringe with Enfit Connection Sterile, REF 401SE

Cardinal Health 200, LLC

FDA Devices Moderate Feb 14, 2024

BD BBL Sensi Disc Minocycline - 30 ug, used for semi-quantitative in vitro susceptibility testing. Catalog Number 231250 and 231251¿

Becton Dickinson & Co.

FDA Devices Moderate Feb 14, 2024

Senographe Pristina

GE Medical Systems, SCS

FDA Devices Critical Feb 14, 2024

Cardinal Health Monoject, 35mL Enteral Syringe (purple) - For Use with ENFit Connection System, REF 435SE

Cardinal Health 200, LLC

FDA Devices Moderate Feb 14, 2024

Ingenia Ambition X (Product Number 781356) - HA FlexTrak II (Accessory Number 989710008732), patient transportation system

Philips North America

FDA Devices Moderate Feb 14, 2024

BD BBL Sensi Disc Cefaclor - 30 ug¿, used for semi-quantitative in vitro susceptibility testing. Catalog Number 231653¿

Becton Dickinson & Co.

FDA Devices Moderate Feb 14, 2024

RX Series Copper (Cu) Assay Ref. Number CU2340

Randox Laboratories Ltd.

FDA Devices Moderate Feb 14, 2024

Spectral CT 7500: Software Version 5.0, Model 728333 and Spectral CT 7500 China: Software Version 5.0, Model 728340.

PHILIPS MEDICAL SYSTEMS

FDA Devices Moderate Feb 14, 2024

BD BBL Sensi Disc Cefotaxime - 30 ug¿, used for semi-quantitative in vitro susceptibility testing. Catalog Number 231606 and 231607¿; 5 ug, Catalog …

Becton Dickinson & Co.

FDA Devices Critical Feb 14, 2024

Cardinal Health Monoject, 20 mL Syringe Luer-Lock Tip Soft Pack, REF 1182000777

Cardinal Health 200, LLC

FDA Devices Critical Feb 14, 2024

Cardinal Health Monoject, 12 mL Syringe Luer-Lock Tip Soft Pack, REF 1181200777T

Cardinal Health 200, LLC

FDA Devices Moderate Feb 14, 2024

BD BBL Sensi Disc Tetracycline 30 ug,used for semi-quantitative in vitro susceptibility testing. Catalog Number 230998 and 231344¿

Becton Dickinson & Co.

FDA Devices Critical Feb 14, 2024

BrightView XCT, gamma camera for SPECT; Model Nos.: 6-digit format 882482; 12-digit format 453560462131 453560749161

Philips North America

FDA Devices Moderate Feb 14, 2024

BD BBL Sensi Disc Meropenem- 10 ug, used for semi-quantitative in vitro susceptibility testing. Catalog Number 231703 and 231704¿

Becton Dickinson & Co.

FDA Devices Moderate Feb 14, 2024

HRIS ACET CUP CUT TIP 26X140 Part Number: 6210-5-100. single-use, sterile surgical instruments used during hip arthroplasty

Howmedica Osteonics Corp.

FDA Devices Moderate Feb 14, 2024

BD BBL Sensi Disc Ceftaroline - 30 ug, used for semi-quantitative in vitro susceptibility testing. Catalog Number 232231¿

Becton Dickinson & Co.

FDA Devices Moderate Feb 14, 2024

BD BBL Sensi Disc Cefepime - 30 ug¿, used for semi-quantitative in vitro susceptibility testing. Catalog Number 231696¿

Becton Dickinson & Co.

FDA Devices Moderate Feb 14, 2024

BD BBL Sensi Disc Imipenem- 10 ug, used for semi-quantitative in vitro susceptibility testing. Catalog Number 231644 and 231645¿

Becton Dickinson & Co.

FDA Devices Critical Feb 14, 2024

1. HeartMate Touch Communication System, REF HMT1100 2. HeartMate Touch Communication System, Rental REF HMT1100-R 3. HeartMate Touch Communication…

Thoratec Corp.

FDA Devices Moderate Feb 14, 2024

Globus Medical Cranial Drill, 6.00mm - instruments for access, preparation, and placement of cranial devices with the ExcelsiusGPS. Ref: 6143.1…

Globus Medical, Inc.

FDA Devices Moderate Feb 14, 2024

BD BBL Sensi Disc Moxifloxacin- 5 ug, used for semi-quantitative in vitro susceptibility testing. Catalog Number 231758¿

Becton Dickinson & Co.

FDA Devices Moderate Feb 14, 2024

BD BBL Sensi Disc Chloramphenicol- 30 ug, used for semi-quantitative in vitro susceptibility testing. Catalog Number 230733¿and 231274¿

Becton Dickinson & Co.

FDA Devices Moderate Feb 14, 2024

Ingenia 1.5T (Product Number 781396) - HA FlexTrak II (Accessory Number 989710008732), patient transportation system

Philips North America

FDA Devices Moderate Feb 14, 2024

Flow-i C20 Anesthesia System, model 6677200

Getinge Usa Sales Inc

FDA Devices Moderate Feb 14, 2024

Globus Medical Cranial Drill with Stop, 2.40mm - Instruments for access, preparation, and placement of cranial devices with the ExcelsiusGPS. Ref : …

Globus Medical, Inc.

FDA Devices Moderate Feb 14, 2024

BD BBL Sensi Disc Ertapenem- 10 ug, used for semi-quantitative in vitro susceptibility testing. Catalog Number 232174 and 232175¿

Becton Dickinson & Co.

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.