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 601 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 2 critical (Class I-equivalent) actions, 21 moderate recalls, and 27 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 30, 2015 to Dec 30, 2015, covering 20 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).
1 Step 12 Panel Cup, Item No. NBCA-12M-W
Ameditech Inc
ProScreen 10 Drug Panel Cassette Test, Item No. PSP-10PPX
Ameditech Inc
DrugSmart 11 Test Cup, Item No. 61127D
Ameditech Inc
iCup DX 12 Panel w/ Adulterant, Item No. I-DXA-1127-023
Ameditech Inc
ProScreen 12 Drug Cup w/Adulteration, Item No. PSCupA-12TBU
Ameditech Inc
Flexible Screw Driver SJ706R; Non Sterile; B Braun; Aesculap; Aesculap AG These instruments are intended for use during the implantation…
Aesculap, Inc.
Immutest 5 Pnl Drug Cup w/ Adult -waived, Item No. IMCA-5AB-W
Ameditech Inc
Syngo Imaging XS is a Picture Archiving and Communication System (PACS)
Siemens Medical Solutions USA, Inc
ProScreen 9 Panel Cup w/Adulterants, Item No. PSCUPA-9BO300
Ameditech Inc
Vancomycin Screen Agar
Becton Dickinson & Co.
DrugSmart Dip (MET/OPI2)+AMP+BZO+COC+THC, Item No. 30600D
Ameditech Inc
ProScProScreen 10 Panel Cup with Adulterants, Item No. PSCupA-10AM
Ameditech Inc
Zimmer UNIVERSAL Power System Loaner and Modular Electric/Battery Single Trigger Handpiece. Rx only Made in Switzerland
Zimmer, Inc.
ProScreen 10 Panel Dip Card, Item No. PSD-10MOX, PSD-10MOB, PSD-10MMO300
Ameditech Inc
Flexible Drill; SJ723R; NON STERILE; B Braun Aesculap; Aesculap AG These instruments are intended for use during the implantations of the A…
Aesculap, Inc.
Label reading in part as: "NexGen System, Complete Knee Solution; Reference Number 5980-37-01; Tibial Component, Precoat, Stemmed Size 3; Lot Numbe…
Zimmer Manufacturing B.V.
ProScreen 10 Panel Cup, Item No. PSCup-10M
Ameditech Inc
IntellaTip MiFi XP Asymmetric (N4) Curve 7/110/2.5/8-8 Material Number: M004PM4500N40; Catalog number: PM4500N4; Cardiac: The IntellaTip MiFi…
Boston Scientific Corp
Dressol-X, Radiopaque D-502, NDC 11004-502-40, Dental Use Only, Active Ingredients: A.S.A. (Acetylsalicylic Acid) + Eugenol
Rainbow Specialty & Health Products
iCup DX 8 Panel w/Adulterant, Item No. I-DXA-187-016
Ameditech Inc
Black Mamba Suture Passer
Biomet, Inc.
ProScreen 12 Panel Cup w/Adult., Item No. PSCupA-12M
Ameditech Inc
ProScreen 6 Panel Dip Card, Item No. PSCuPSD-6BUP300, PSD-6MTDBO300, PSD-6BUPO, PSD-6MBO, PSD-6MB,
Ameditech Inc
ProScreen 5 Panel Dip Card, Item No. PSD-12BUP
Ameditech Inc
Terumo Surflo Winged Infusion Set with Filter and Needle Protection (Surshield), Product Code: SV-S25FL35.
Terumo Medical Corp
Alaris Pump SmartSite Infusion Set, Model No. 2420-0500. Used to administer fluid and medications through a needle or catheter inserted into the p…
CareFusion 303, Inc.
Ingenuity Core 128 Computed Tomography X-ray system
Philips Medical Systems (Cleveland) Inc
ProScreen 7 Panel Dip Card, Item No. PSD-7MPB, PSD-7MO, PSD-7M
Ameditech Inc
DrugSmart 12 Test Cup (Multi & BUP), Item No. 61210D DrugSmart 12 Test Cup (Multi/Single/BUP), Item No. 61205D
Ameditech Inc
ProScreen 6 Panel Cup w/Adult (AU), Item No. PSCupA-6MBAU
Ameditech Inc
11 Panel Dip Card (OPI 300) w/Adult, Item No. 11125AA
Ameditech Inc
Reagent Management System (RMS) Dimension EXL with LM STM Product Usage: The Reagent Management System (RMS) is a module for use with the Dimen…
Siemens Healthcare Diagnostics Inc.
ProScreen 5 Panel Dip Card w/Adult, Item No. PSDA-5MB300
Ameditech Inc
Synaptive Medical BrightMatter Navigator System (Guide System). Part number SYN-0026. The Guide system is comprised of a cart labelled SYN-0024 and …
Synaptive Medical, Inc.
Optional PS500 Power Supply Unit for the Evita V500 Ventilator and Babylog VN500 Ventilator. Babylog VN500 is a ventilation unit intended for the …
Draeger Medical, Inc.
THERMO FISHER 8 DRUG CASSETTE, Item No. MTPA-8MBAU
Ameditech Inc
CLIA RDTC 12-Panel Cup (w/Adulteration), Item No. CLIA-RDTC-12, DCC-81205-5
Ameditech Inc
Micro Screen 6 Panel Cup with Adult (AU), Item No. MSCA-6MBAU
Ameditech Inc
Etest¿ PIP/TAZO/CON-4 PTC 256 -pack of 30 tests US. Etest¿ is a quantitative technique for determining the antimicrobial susceptibility of Gram-ne…
Biomerieux
DrugSmart Cup THC/COC/AMP//MET/OPI2/BZO, Item No. 60600D
Ameditech Inc
ProScreen CLIA Waived Cup with 8 Drug, Item No. PSCup-8P-W
Ameditech Inc
MicroCutter Xchange 30 Blue Cartridge, FG-025320; The MicroCutter XCHANGE 30 Blue Cartridge and MicroCutter XCHANGE 30 Blue Curved Tip Cartridge con…
Cardica, Inc.
Green Mamba Suture Passer
Biomet, Inc.
Ingenuity Core Computed Tomography X-ray system
Philips Medical Systems (Cleveland) Inc
FB Broth, 10ml (Fastidious Bacteria Broth) Cat. no: K31 Lot: 15231 A fastidious bacteria broth for the enriched cultivation of Neisseria spp.,…
Hardy Diagnostics
iCup DX 10 Panel w/Adulterant, Item No. I-DXA-1107-142
Ameditech Inc
12-Panel Dip Drug Screen with adulterant, Item No. PSDA-12BUP, PSD-6MTDBO300, PSD-10PPX, PSD-10MOX, 60960D, 61127D, DCC-81205-5, IMCA-10M5.
Ameditech Inc
IntellaTip MiFi XP Asymmetric (N4) Curve 7/110/2.5/8-10 ; Material Number: M004PM4790N40; Catalog number: PM4790N4; Cardiac: The IntellaTip M…
Boston Scientific Corp
Airways Development LLC WaterPAP Positive Airway Pressure Device Reference #WP-7700.
Airways Development LLC
Factor VIII Chromogenic Assay, REF/Catalog No. B4238-40, Siemens Material Number (SMN) 10445729, IVD. --- CLASSIFICATION NAME: Test, Qualitative and…
Siemens Healthcare Diagnostics, 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.