PlainRecalls
2023 data Federal recall API Linked to agency record

FDA Medical Devices

All recall actions attributed to FDA Medical Devices in our federal database. Each record links back to the agency's official notice so you can verify status, remedy, and amendments before acting.

U.S. Food and Drug Administration — Medical device recalls

39,794 recalls · Page 163 of 796

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FDA Medical Devices Recall Insight

According to PlainRecalls' agency ranking (distinct recall events, same sort as /agency), FDA Medical Devices sits #1 of 6 (1st among 6 issuing agencies) with 39,794 notices, about 38.1% of the 104,423-record archive. The agency's stated scope - U.S. Food and Drug Administration — Medical device recalls - determines what classes of products flow through its recall pipeline and how quickly notices reach consumers. With 796 pages of records at 50 recalls per page, this archive represents one of the longest continuous federal enforcement histories accessible to the public.

Looking at the 50 records on this page alone, the severity distribution skews toward 3 critical (Class I-equivalent) actions, 47 moderate recalls, and 0 lower-severity notices. Approximately 50 of 50 entries name a specific recalling firm, while 44 disclose a unit count, the gap reflects regulatory filing norms where firms disclose lot numbers or distribution channels instead of absolute quantities. This page spans recalls from Jan 17, 2024 to Jan 24, 2024, covering 29 distinct firms. Severity mix is a leading indicator: a page weighted toward critical classifications usually signals an active public-health concern, while lower-severity clusters often represent labeling, undeclared-allergen, or minor design corrections.

Agency-level browsing is useful when a defect pattern crosses categories, for example, a supplier contamination can trigger dozens of downstream recalls that share no obvious product tag but a single issuing agency. Use the pagination below to scan the full archive, or combine this agency filter with category and manufacturer views elsewhere on PlainRecalls to intersect the data. Recall records are sourced directly from FDA Medical Devices's public enforcement feeds and are updated as the agency publishes new notices; the federal record is the authoritative version, and this page aggregates what the agency itself has released. For high-stakes decisions, medical, automotive, or childcare, always click through to the recall detail page and cross-verify the recall number against the agency's current site. Record counts reflect all indexed actions regardless of status (ongoing, terminated, or completed).

Critical Jan 24, 2024

Distal Phasitron, Part: S20020, for use with Percussionaire VDR-4 control driver (or control unit)

Percussionaire Corporation

Moderate Jan 24, 2024

(1) CareEvent, Model No. 866435 (2) CareEvent Upgrade, Model no. 866436

Philips North America

Critical Jan 24, 2024

Product REF 4000-100N, DRAIN, EXPRESS SINGLE W/AC, Single Collection

Maquet Cardiovascular, LLC

Moderate Jan 24, 2024

Maquet Prismalix OR Light Systems, Model Numbers and Catalog Numbers 3001 - ARD567424001C, 3001 HMS07 - ARD567722001C, 3001 HXS12 - ARD567703001C, 4001 S/DF - ARD567211211C, 4001 SAD/DF - ARD567221211C, 4001 SAD/DF - ARD567221241C, 4001 SAD/SF - ARD567221141C, 4001 SAI/DF - ARD567220111C, 4001K S/DF - ARD567211213C, 4003 - ARD567215111C, 4401 S/DF - ARD567212211C, 4401 SAD/DF - ARD567223211C, 4401 SAD/DF - ARD567223241C, 4401 SAD/SF - ARD567223111C, 4441 SAD/DF - ARD567225241C, 6001K ACS/T - ARD

Getinge Usa Sales Inc

Moderate Jan 24, 2024

Ultrasound EA (Ergonomic Advantage) table versions; G3 (General 3 Section) Echocardiography -An Ultrasound examination table

Oakworks Inc

Moderate Jan 24, 2024

Ultrasound EA (Ergonomic Advantage) table version; V2 (Vascular 2 Section) Echocardiography -An Ultrasound examination table

Oakworks Inc

Moderate Jan 24, 2024

6IN PRESSURE TUBING, List Number MX20617

Smiths Medical Asd Inc

Moderate Jan 24, 2024

Vasoview Hemopro Endoscopic Vessel Harvesting System, model VH-3500.

Maquet Cardiovascular, LLC

Critical Jan 24, 2024

ExcelsiusGPS Flat Panel Fluoroscopy Fixture Kit, Part number 6203.2100

Globus Medical, Inc.

Moderate Jan 24, 2024

GammaPod - Treatment Planning System-a component of the GammaPod Irradiation System. Ref: XMSGP030A09.07-0.01 Intended for use in the noninvasive stereotactic delivery of a radiation dose to a partial volume of the breast in conjunction with breast conserving treatment.

Xcision Medical Systems, LLC

Moderate Jan 24, 2024

PRIMA TT Glenoid Monoblock/Modular reverse TT baseplates: Description/Product Code: BASEPLATE D.25MM REGULAR/1975.14.500, BASEPLATE D.28MM REGULAR/1975.14.800, BASEPLATE D.25MM FULL WEDGED 10-degrees/1975.14.510, BASEPLATE D.28MM FULL WEDGED 10-degrees/1975.14.810, BASEPLATE D.25MM FULL WEDGED 15-degrees/1975.14.615, BASEPLATE D.28MM FULL WEDGED 15-degrees/1975.14.815, BASEPLATE D.28MM FULL WEDGED 15-degrees X/1975.14.865, BASEPLATE D.25 MM FULL WEDGED 20-degrees/1975.14.620, BASEPLATE

Limacorporate S.p.A

Moderate Jan 24, 2024

Curaplex Field Cric Kit with ET Tube, Item Number 36611. The kit provides healthcare professionals with an assortment of supplies to perform a cricothyrotomy.

Sarnova HC, Llc

Moderate Jan 24, 2024

INDICAID COVID-19 Rapid Antigen At-Home Test, REF: P0040

PHASE SCIENTIFIC INTERNATIONAL LIMITED

Moderate Jan 24, 2024

Medex LOGICAL CATH LAB KIT, List Number M20754

Smiths Medical Asd Inc

Moderate Jan 24, 2024

Soltive SuperPulsed Laser System TFL FIBER CLEAVER, Model Number TFL-AFC

Olympus Corporation of the Americas

Moderate Jan 24, 2024

20IN (50.8CM) BRAIDED INJ LINE, ROTATING ADAPT, List Number MX682BR

Smiths Medical Asd Inc

Moderate Jan 24, 2024

Calibration Serum Level 3. CAL 3, REF CAL2351. Human Assayed Multi-Sera Level 2 (HN1530) Human Assayed Multi-Sera Level 3 (HE 1532)

Randox Laboratories Ltd.

Moderate Jan 24, 2024

Spectral CT 7500, Software Version 5.0.0.X. Computed Tomography X-Ray System.

Philips North America Llc

Moderate Jan 24, 2024

Maquet Orchide OR Light Systems, Model Numbers and Catalog Numbers OHDII FHD QL VP01 - ARD568803935, OHDII FHD QL AIR03 U - ARD568803952, OHDII FHD QL AIR03 E - ARD568803967, OHDII FHD QL AIR04 E/U - ARD568803968, OHDII FHD QL+ VP01 - ARD569204944, OHDII AIR03 QL FHD E - ARD568803951

Getinge Usa Sales Inc

Moderate Jan 24, 2024

Medex 700PSI STOPCOCK W/ROTATOR, List Number MX4331R

Smiths Medical Asd Inc

Moderate Jan 24, 2024

Ultrasound EA (Ergonomic Advantage) table versions; G2 (GENERAL 2) -An Ultrasound examination table

Oakworks Inc

Moderate Jan 24, 2024

TECNIS Toric II OptiBlue IOL Models ZCW

Johnson & Johnson Surgical Vision, Inc.

Moderate Jan 24, 2024

PosiFlush Prefilled Saline Syringe with General Pump Compatibility (10mL Syringe with 10mL Saline Fill), Catalog Number 306547

Becton Dickinson & Company

Moderate Jan 24, 2024

FreeStyle Libre 3 App, part of Continuous Glucose Monitoring System, when used on the Android 13 Operating System

Abbott Diabetes Care, Inc.

Moderate Jan 17, 2024

Model No. CYF-V2, VISERA Cysto-Nephro Videoscope

Shirakawa Olympus Co., Ltd.

Moderate Jan 17, 2024

Sensis Vibe Hemo

Siemens Medical Solutions USA, Inc

Moderate Jan 17, 2024

OLYMPUS ENDOEYE FLEX DEFLECTABLE VIDEOSCOPE (5.4 mm diameter) Model: LTF-S190-5 Used with a video system center, light source, documentation equipment, monitor, hand instruments, electrosurgical unit, and other ancillary equipment for endoscopy and endoscopic surgery within the thoracic and abdominal cavities, including female reproductive organs.

Olympus Corporation of the Americas

Moderate Jan 17, 2024

Scoot Control R-net, Product Number P015-61. The Scoot Control is intended to support a wheelchair attendant in controlling or maneuvering a power chair

mo-Vis BVBA

Moderate Jan 17, 2024

Abiomed Kit, 14Fr Introducer, 13cm&25cm, Sterile Part of Pump Set (0048-0040, 0048-0045, 1000080)-Introducer(s) are intended for introduction of the Impella Catheter into the body. Part Number: 0052-3046

Abiomed, Inc.

Moderate Jan 17, 2024

Baxter Flo-Thru Intraluminal Shunt, Product Codes: a) Product Code FT12100, 1.00 GLOBAL; b) Product Code FT12125, 1.25 GLOBAL; c) Product Code FT12150, 1.50 GLOBAL; d) Product Code FT12175, 1.75 GLOBAL; e) Product Code FT12200, 2.00 GLOBAL; f) Product Code FT12225, 2.25 GLOBAL; g) Product Code FT12250, 2.50 GLOBAL; h) Product Code FT12275, 2.75 GLOBAL; i) Product Code FT12300, 3.00 GLOBAL

Baxter Healthcare Corporation

Moderate Jan 17, 2024

Oscor Intro Kit, 14Fr x 13 and 25 cm Part of Pump Set (0048-0040)-Introducer(s) are intended for introduction of the Impella Catheter into the body. Part Number: 0052-3025

Abiomed, Inc.

Moderate Jan 17, 2024

Baxter Floseal Hemostatic Matrix Fast Prep, Product Codes: a) ADS201844, 5 mL b) ADS201845, 10mL

Baxter Healthcare Corporation

Moderate Jan 17, 2024

The BIOFIRE Respiratory Panel 2.1 (RP2.1) is a PCR-based multiplexed nucleic acid test intended for use with the BIOFIRE FILMARRAY 2.0 or BIOFIRE FILMARRAY Torch Systems.

BioFire Diagnostics, LLC

Moderate Jan 17, 2024

SPRYSTEP VECTOR KAFO, Custom made device dynamic ankle-foot orthosis (KAFO) non locking, REF #s: 17VKCUS and 17VKCUSX

Townsend Design

Moderate Jan 17, 2024

QMS Tacrolimus Calibrators, Product code 10015573

Ortho-Clinical Diagnostics, Inc.

Moderate Jan 17, 2024

VADER pedicle system, torque wrench, Catalog Number 42-702

Icotec Ag

Moderate Jan 17, 2024

Model No. CYF-VH, CYSTO-NEPHRO VIDEOSCOPE

Shirakawa Olympus Co., Ltd.

Moderate Jan 17, 2024

BrightView X, Gamma Camera, Product Code 882478

Philips North America

Moderate Jan 17, 2024

(1) Ingenia Ambition X (Product Number 781356); (2) Ingenia Ambition S (Product Number 781359)

Philips North America

Moderate Jan 17, 2024

CORI REAL INTELLIGENCE Robotic Drill, Product No. ROB10013 and ROB10013S

Blue Belt Technologies, Inc

Moderate Jan 17, 2024

Alinity i Processing Module REF 03R65-01 The Alinity i Processing Module is a fully automated immunoassay analyzer allowing random and continuous access, as well as priority and automated retest processing using chemiluminescent microparticle immunoassay (CMIA) technology. CMIA technology is used to determine the presence of antigens, antibodies, and analytes in samples.

Abbott Laboratories

Moderate Jan 17, 2024

Vascu-Guard Peripheral Vascular Patch (US), Product Codes: a) VG0108: 0.8 X 8 CM US, TS; b) VG0110: 1 X 10 CM US, TS; c) VG0106: 1 X 6 CM US, TS; d) VG0209: 2 X 9 CM US, TS

Baxter Healthcare Corporation

Moderate Jan 17, 2024

Medtronic, REF 9733235, Pin, 100mm, STERILE, PERCUTANEOUS

Medtronic Navigation, Inc.

Moderate Jan 17, 2024

Abiomed Axillary Insertion Introducer -Introducer(s) are intended for introduction of the Impella Catheter into the body. Part Number: 0052-3006 Individual, and Part of Pump Set (005062, 0550-0008, 1000100, 0052-0011, 1000220)

Abiomed, Inc.

Moderate Jan 17, 2024

Abiomed Kit, 14Fr Introducer, 25cm, Long Taper Individual (0052-0039)-Introducer(s) are intended for introduction of the Impella Catheter into the body. Part Number: 0052-0053

Abiomed, Inc.

Moderate Jan 17, 2024

XScribe CP Cardiac Stress Testing System, version 6, with below product names and codes: a) X-SCRIBE CPI KIT WIRELESS USB 608 MHz, 41000-030-50; b) X-SCRIBE CPI KIT WIRELESS USB 2500 MHz, 41000-030-51; c) X-SCRIBE CPI KIT DIRECT CONNECT USB, 41000-030-52; d) X-SCRIBE CPI KIT QUICK CONNECT USB, 41000-030-53; e) XSCRIBE CP KIT WIRELESS, 41000-030-60; f) XSCRIBE CP KIT WIRED, 41000-030-62; g) XSCRIBE CP SW KIT, 41000-030-64

Baxter Healthcare Corporation

Moderate Jan 17, 2024

Model No. CYF-VHR, CYSTO-NEPHRO VIDEOSCOPE

Shirakawa Olympus Co., Ltd.

Moderate Jan 17, 2024

Baxter FloSeal Hemostatic Matrix NL, 5 mL, Product Codes: ADS201883

Baxter Healthcare Corporation

Moderate Jan 17, 2024

Baxter Flo-Rester, Disposable internal vessel occluder, distributed in the following sizes: a) Product Code 50100: 12MM, 1.00 MM GLOBAL; b) Product Code 50150: 12MM, 1.50 MM GLOBAL; c) Product Code 50175: 12MM, 1.75 MM GLOBAL; d) Product Code 50200: 12MM, 2.00 MM GLOBAL; e) Product Code 50225: 12MM, 2.25 MM GLOBAL; f) Product Code 50250: 12MM, 2.50 MM GLOBAL; g) Product Code 50275: 12MM, 2.75 MM GLOBAL; h) Product Code 50300: 12MM, 3.00 MM GLOBAL; i) Product Code 5

Baxter Healthcare Corporation

Moderate Jan 17, 2024

Alinity c Processing Module REF 03R67-01 The Alinity c Processing Module is a fully automated chemistry analyzer allowing random and continuous access, as well as priority and automated retest processing using photometric and potentiometric detection technology. The Alinity c Processing Module uses photometric detection technology to measure sample absorbance for the quantification of analyte concentration and uses potentiometric detection technology to measure the electrical potential

Abbott Laboratories

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Disclaimer: This information is provided for informational purposes only and does not constitute professional advice. Consult a qualified professional before making decisions based on this data.

Every figure on PlainRecalls is rendered directly from official FDA, CPSC, USDA FSIS and NHTSA recall records; no number is typed in by an editor. Recall counts and figures reflect FDA Medical Devices's own published filings, aggregated alongside the other two federal recall feeds. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of September 2026.