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

39,096 recalls · Page 663 of 782

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FDA Medical Devices Recall Insight

PlainRecalls tracks 39,096 recall actions attributed to the FDA Medical Devices in our federal recall index. Across the full PlainRecalls database of 101,704 records spanning 1995 through the present, FDA Medical Devices accounts for roughly 38.4% of all indexed recalls. 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 782 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 1 critical (Class I-equivalent) actions, 41 moderate recalls, and 8 lower-severity notices. Approximately 50 of 50 entries name a specific recalling firm, while 50 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 Nov 26, 2014 to Dec 3, 2014, covering 22 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).

Moderate Dec 3, 2014

8MM,BLACK DIAMOND MICRO FORCEPS; Intended to assist in the accurate control of Intuitive Surgical Endoscopic Instruments.

Intuitive Surgical, Inc.

Moderate Dec 3, 2014

8MM,LARGE NEEDLE DRIVER; Intended to assist in the accurate control of Intuitive Surgical Endoscopic Instruments.

Intuitive Surgical, Inc.

Moderate Dec 3, 2014

8MM PERMANENT CAUTERY SPATULA,; Intended to assist in the accurate control of Intuitive Surgical Endoscopic Instruments.

Intuitive Surgical, Inc.

Moderate Dec 3, 2014

Esprit V1000 Ventilator and Esprit/V200 Conversion Ventilator The Esprit V1000 and Esprit/V200 Conversion Ventilators are microprocessor-controlle…

Respironics California Inc

Low Dec 3, 2014

LUNA Chest, Model No. LU4006

Novadaq Technologies, Inc.

Moderate Dec 3, 2014

IntelliSpace Portal DX/HX/EX model number: 881001 IntelliSpace Portal DX/HX/EX Upgrade model number: 881011 IntelliSpace Portal DX/HX/EX Demo model…

Philips Medical Systems (Cleveland) Inc

Moderate Dec 3, 2014

8MM, SMALL GRASPING RETRACTOR ; Intended to assist in the accurate control of Intuitive Surgical Endoscopic Instruments.

Intuitive Surgical, Inc.

Moderate Dec 3, 2014

8MM,PROGRASP FORCEPS; Intended to assist in the accurate control of Intuitive Surgical Endoscopic Instruments.

Intuitive Surgical, Inc.

Low Dec 3, 2014

Non-sterile drape

Novadaq Technologies, Inc.

Moderate Dec 3, 2014

8MM FENESTRATED BIPOLAR FORCEPS,; Intended to assist in the accurate control of Intuitive Surgical Endoscopic Instruments.

Intuitive Surgical, Inc.

Moderate Dec 3, 2014

7F NeuroFlo Catheter, Model 1027 The NeuroFlo Catheter is a multi-lumen device with two balloons mounted near the distal tip for the treatment of …

ZOLL Circulation, Inc.

Moderate Dec 3, 2014

8MM, ATRIAL RETRACTOR SHORT RIGHT ; Intended to assist in the accurate control of Intuitive Surgical Endoscopic Instruments.

Intuitive Surgical, Inc.

Moderate Dec 3, 2014

Trabecular Metal Tibial Impactor. Product Usage: TM Tibial Impactor pads are used in conjunction with the TM Tibial Impactor to impact the tibial…

Zimmer, Inc.

Moderate Dec 3, 2014

Cardiac Function Analysis Software Product Data No. MPDCT0301EAD CSCF-003A The software is applicable to the following CT systems: Aquilion ONE T…

Toshiba American Medical Systems Inc

Moderate Dec 3, 2014

Zimmer Patient Specific Instrument PERSONA CR Pin Guides (Femur and Tibia) is intended to be used as a surgical instrument to assist in the positioni…

Materialise USA LLC

Moderate Dec 3, 2014

8MM, LARGE HEM-O-LOK CLIP APPLIER; Intended to assist in the accurate control of Intuitive Surgical Endoscopic Instruments.

Intuitive Surgical, Inc.

Critical Dec 3, 2014

Gel-E Donut : 92025-A (Extra Small), 92025-B (Small), 92025-C (Medium) and Squishon 2 91033-2. The products are intended to support and cradle a…

Philips Medical Systems, Inc.

Moderate Dec 3, 2014

CooperSurgical LEEP RADIUS LOOP ELECTRODE (W 2.0 cm x D 1.0 cm D, 12 cm shaft ). Box of 5 Model Number(s): R2010 Intended Use: Diagnosis and treatm…

CooperSurgical, Inc.

Moderate Nov 26, 2014

UPGRD PRGM 9734638 ADD AxiEM NAVIGATION

Medtronic Navigation, Inc.

Moderate Nov 26, 2014

DRAPE 9732722 TUBE STERILE O-ARM 20PK

Medtronic Navigation, Inc.

Moderate Nov 26, 2014

TUMOR RES. PACK 9733553 AxiEM S.M.

Medtronic Navigation, Inc.

Moderate Nov 26, 2014

MOSAIQ Product Usage: MOSAIQ is an oncology information system used to manage workflows for treatment planing and delivery. It supports informati…

Elekta, Inc.

Low Nov 26, 2014

Etest¿ Ceftaroline (CPT32) US B100. Etest¿ (Antimicrobial Susceptibility Testing) is a quantitative technique for determining the antimicrobial su…

Biomerieux

Moderate Nov 26, 2014

CyberKnife Robotic Radiosurgery System with the first generation IRIS Variable Aperture Collimator. The CyberKnife is indicated for treatment plan…

Accuray Incorporated

Moderate Nov 26, 2014

The MectaLIF Oblique Handle, model number 03.22.10.0262, is used to insert the MectaLIF oblique spinal cage implants.

Medacta Usa

Moderate Nov 26, 2014

Transport Chair and Rollator in 1, Model HE21630011 Burgundy and HE21630011 Blue. This is a walker/rolling chair. Used to assist injured and infir…

Silver Star Brands

Moderate Nov 26, 2014

KIT, 9731427, THORACIC TACTILE PROBES

Medtronic Navigation, Inc.

Low Nov 26, 2014

Etest¿ Ceftaroline (CPT32) WW B30. Etest¿ (Antimicrobial Susceptibility Testing) is a quantitative technique for determining the antimicrobial sus…

Biomerieux

Moderate Nov 26, 2014

Nidek MC-500 Multicolor Laser Photocoagulator using software version 2.20. Opthalmic Device. The Nidek Multicolor Laser photocoagulator Model MC-500…

Nidek Inc

Moderate Nov 26, 2014

ENT PRGM 9734636 ADD FUSION NAV AxiEM

Medtronic Navigation, Inc.

Moderate Nov 26, 2014

MOUSE 9732721 STERILE O-ARM 10PK

Medtronic Navigation, Inc.

Moderate Nov 26, 2014

FullFire Diffusing Tip Laser Probe, REF: DTP101-01, DTP201-01, DTP301-01, DTP401-01, DTP501-01. These laser probes are part of the NeuroBlate Syste…

Monteris Medical Corp

Low Nov 26, 2014

Etest¿ Ceftaroline (CPT32) US B30. Etest¿ (Antimicrobial Susceptibility Testing) is a quantitative technique for determining the antimicrobial sus…

Biomerieux

Moderate Nov 26, 2014

SideFire Directional Laser Probe, REF: NBP101-01, NBP201-01, NBP301-01, NBP401-01, NBP501-01. These laser probes are part of the NeuroBlate System,…

Monteris Medical Corp

Moderate Nov 26, 2014

SPHERES 8801071 1/TRAY 12PK

Medtronic Navigation, Inc.

Moderate Nov 26, 2014

TRAJ GUIDE KIT, 9733065, BIOPSY, EXT

Medtronic Navigation, Inc.

Moderate Nov 26, 2014

BIT 9733516 2.9mm DRILL STERILE

Medtronic Navigation, Inc.

Moderate Nov 26, 2014

SPHERES 8801075 5/TRAY 12PK

Medtronic Navigation, Inc.

Low Nov 26, 2014

Etest¿ Ceftaroline (CPT32) WWB100. Etest¿ (Antimicrobial Susceptibility Testing) is a quantitative technique for determining the antimicrobial sus…

Biomerieux

Low Nov 26, 2014

ADVIA Centaur¿ and ADVIA Centaur¿ XP and ADVIA Centaur¿ CP Cleaning Solution (For in vitro diagnostic use with the ADVIA¿ Centaur systems) Catalog N…

Siemens Healthcare Diagnostics, Inc

Moderate Nov 26, 2014

TUMOR RESECTION KIT 9733607 NON-INVASIVE

Medtronic Navigation, Inc.

Moderate Nov 26, 2014

SHUNT KIT 9733605 NON-INVASIVE

Medtronic Navigation, Inc.

Moderate Nov 26, 2014

INSTRUMENT TRACKER 9733533XOM ENT 1PK

Medtronic Navigation, Inc.

Moderate Nov 26, 2014

10 mm/135 degree Titanium Cannulated Trochanteric Fixation Nail 170 MM - Sterile: intended to treat stable and unstable fractures of the proximal fem…

Synthes, Inc.

Moderate Nov 26, 2014

DISP 9730950 STRL SPHERE, 1 PK INSERT

Medtronic Navigation, Inc.

Moderate Nov 26, 2014

TRAJ GUIDE KIT, 9733066, BIOPSY, INT

Medtronic Navigation, Inc.

Moderate Nov 26, 2014

Edwards Lifesciences Vent Catheters, . Packaged sterile and non-pyrogenic in a sealed, peel-type pouch. Model Numbers: E061, E060, PE062, EM012 At…

Edwards Lifesciences, LLC

Low Nov 26, 2014

ADVIA Centaur BNP Assay for in vitro diagnostic use in the quantitative determination of B-type Natriuretic Peptide (BNP) in human plasma using the A…

Siemens Healthcare Diagnostics, Inc

Moderate Nov 26, 2014

PIN, 9733236, 150MM, STERILE, PERC REF

Medtronic Navigation, Inc.

Moderate Nov 26, 2014

AxoTrack I Sterile Procedure Kit 18G, K1001-18XTW, (24/case labeled for US, 5/case labeled for US, 24/case labeled for EU, 5/case labeled for EU). …

Soma Access Systems LLC

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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.

Compiled from official public sources by the editorial team.

Every figure on PlainRecalls is rendered directly from official FDA, CPSC 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 July 2026.