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 602 of 782
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 3 critical (Class I-equivalent) actions, 24 moderate recalls, and 23 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 Dec 23, 2015 to Dec 30, 2015, 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).
DrugCheck Waived 12 Panel Cup w/Adult, Item No. DCC-81205-5
Ameditech Inc
ProScreen 6 Panel Dip Drug Screen, Item No. PSD-6BUPO3
Ameditech Inc
Artis systems with large display from Siemens Medical Solutions USA, Inc. Interventional Fluoroscopic X-ray for angiographic procedures.
Siemens Medical Solutions USA, Inc
Etest¿ PIP/TAZO/CON-4 PTC 256 - Foam of 100 tests WW. Etest¿ is a quantitative technique for determining the antimicrobial susceptibility of Gram-…
Biomerieux
Immutest 11 Pnl Drug Screen Cup w/ Adult, Item No. IMCA-11OP
Ameditech Inc
ProScreen 10 Panel Dip Card w/Adult, Item No. PSDA-10MO, PSDA-10MMO300, PSDA-10PPX, PSDA-10BUP, PSD-12BUP, PSD-10M, PSCupA-6MB-W, PSCup-10MMO300, P…
Ameditech Inc
Boston Scientific, Chariot ST-CCV Guiding Sheath, Sterilized using ethylene oxide: Product Description Material Number (UPN) Guiding Sheath 5F, 4…
Boston Scientific Corporation
Tray Set containing multiple instruments and may contain the flexible bone awl, flexible drill and/or flexible screw driver in varying amounts depend…
Aesculap, Inc.
BD Vacutainer K2 EDTA (K2E) 5.4mg Plus Blood Collection Tubes. Product Usage: BD Vacutainer¿ tubes are used to collect, transport and process bl…
Becton Dickinson & Company
ProScreen 8 Panel Dip Card w/Adult, Item No. PSDA-8P, PSDA-8MBO300
Ameditech Inc
THERMO FISHER 6 DRUG CASSETTE, Item No. MTPA-6MBAU
Ameditech Inc
ProScreen 8 Panel Dip Card, Item No. PSD-8P
Ameditech Inc
Cardinal Health Tiny Toes; 11470-010T Infant heel warmer
Philips Electronics North America Corporation
ProScreen 8 Panel Dip Card w/Adult, Item No. PSDA-8P, PSDA-8MBO300
Ameditech Inc
A.L.P.S. 4.0mm Cancellous Locking Screws intended for use in stabilization and fixation of fractures, revision procedures, fusions, reconstructions…
Biomet, Inc.
Immutest Cup CLIA Waived w/Adulteration, Item No. IMCA-7MT-W
Ameditech Inc
DrugSmart 10 Test Cup (PCP & OXY), Item No. 61020D
Ameditech Inc
DA-2006P - Defibrillator / Pacer Analyzer; Product Usage: Intended to measure the output of a defibrillator or transcutaneous pacemaker.
BC Group International Inc
DrugSmart Dip AMP/OPI2/COC/THC/BZO Test, Item No. 30520D
Ameditech Inc
ProScreen 6 Panel Dip Card w/Adult (AU), Item No. PSDA-6MBAU
Ameditech Inc
ProScreen 12 Panel Dip Card, Item No. PSD-12BUP
Ameditech Inc
IntellaTip MiFi XP Asymmetric (N4) Curve, 7/110/2.5/8-8 OUS; Material Number: M004EPM4500N40; Catalog number: EPM4500N4; Cardiac: The Intella…
Boston Scientific Corp
Etest¿ Piperacillin/tazobactam (4 ug/mL) PTc0.016-256-pack of 30 tests WW Etest¿ is a quantitative technique for determining the antimicrobial sus…
Biomerieux
ProScreen CLIA Wvd 12 Panel Cup w/Adult., Item No. PSCupA-12M-W
Ameditech Inc
Reagent Management System (RMS) Dimension RxL Max HM STM Product Usage: The Reagent Management System (RMS) is a module for use with the Dimens…
Siemens Healthcare Diagnostics Inc.
Brilliance iCT SP Computed Tomography X-ray system
Philips Medical Systems (Cleveland) Inc
Flexible Bone Awl; SJ607R; NON STERILE; B Braun Aesculap; Aesculap AG: These instruments are intended for use during the implantations of …
Aesculap, Inc.
RealityCHECK Tilt Cup 12 Panel + Adult, Item No. RC12TCA
Ameditech Inc
Zimmer UNIVERSAL Power System Loaner and Modular Electric/Battery Double Trigger Handpiece. Rx only Made in Switzerland
Zimmer, Inc.
iCup DX 11 Panel w/ Adulterant, Item No. I-DXA-1117-131
Ameditech Inc
Brilliance 64 Computed Tomography X-ray system
Philips Medical Systems (Cleveland) Inc
DrugSmart 9 Test Cup (BUP), Item No. 60960D
Ameditech Inc
VAPR¿ TRIPOLAR 90" Degree Suction Electrodes (Model/Catalog No: 225028)
DePuy Mitek, Inc., a Johnson & Johnson Co.
ProScreen CLIA Waived Cup 6 Drugs w/Adul, Item No. PSCupA-6MB-W
Ameditech Inc
Alaris EtCO2 Module, Model 8300. A capnograph that continuously monitors end tidal carbon dioxide (EtCO2), fractional inspired carbon dioxide (FiCO2…
CareFusion 303, Inc.
MAGNETOM systems, magnetic resonance diagnostic devices (MRDD).
Siemens Medical Solutions USA, Inc
ImmuTest 12 Panel Dip Card, Item No. IMD-12MO3
Ameditech Inc
6 Panel Cup Body and Lid w/Adult (AU), Item No. TDDA-6MBAU-CUP
Ameditech Inc
IntellaTip MiFi XP Asymmetric (N4) Curve 7/110/2.5/8-10 OUS; Material Number: M004EPM4790N40; Catalog number: EPM4790N4; Cardiac: The Intella…
Boston Scientific Corp
Zimmer Oscillating Flat - TS ST Hub; 75mm x 19mm x 1.00/1.27mm; Synvasive Part No. 11-4770: Part No. 19075127YT1; Lot No. 45104 and 43054 …
Synvasive Technology Inc
MicroCutter Xchange 30 Blue Curved Tip Cartridge. Model Number: FG-025321; The MicroCutter XCHANGE 30 Blue Cartridge and MicroCutter XCHANGE 30 Blue…
Cardica, Inc.
EDI BZO Uncut Sheet - Cup*, Item No. 160170
Ameditech Inc
Total Toe Instrument Kit, Labeled in part: "Instrument Set, 15mm Toe, Dorsal Flange Combi" Part Number: 9000-3002 The component in question is th…
Arthrosurface, Inc.
Reagent Management System (RMS) Dimension EXL with LM Product Usage: The Reagent Management System (RMS) is a module for use with the Dimension…
Siemens Healthcare Diagnostics Inc.
Dressit-X, Radiopaque D-545, NDC 11004-545-40, Dental Use Only, Active Ingredients: Eugenol Oil
Rainbow Specialty & Health Products
ProScreen 6 Panel Cassette w/Adult (AU), Item No. PSPA-6MBAU
Ameditech Inc
Reagent Management System (RMS) Dimension RxL Max w/o HM Product Usage: The Reagent Management System (RMS) is a module for use with the Dimensio…
Siemens Healthcare Diagnostics Inc.
Unolok Blunt Fill Needle 18G x 1.5" Red, Sterile, Single use, Non-injectable needle, Single use, non-injection needle
Myco Medical Supplies Inc
MYLA CLINIC PATCH 3.2.0 CD Product Usage: MYLA is a computer application (Middleware) based on Web 2.0 technology which: Interfaces between the…
bioMerieux, Inc.
UniCel DxH 600 Coulter Cellular Analysis System, Software Version 3.0.2.0, Part No. 775222 The UniCel DxH 800/DxH 600 analyzers are quantitative, mu…
Beckman Coulter Inc.
Nearby Agencies
Explore recalls from other federal agencies that share oversight of product safety.
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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.
- Source: FDA Medical Devices - verify with the issuing agency: official recall page →
- Source: PlainRecalls Data Index - aggregated from FDA openFDA, CPSC, and NHTSA public databases
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.