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 479 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 0 critical (Class I-equivalent) actions, 50 moderate recalls, and 0 lower-severity notices. Approximately 50 of 50 entries name a specific recalling firm, while 49 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 Feb 7, 2018 to Feb 7, 2018, covering 12 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).
Affixus Hip Fracture Nail, RH 130 DEG 11MM X 440MM
Zimmer Biomet, Inc.
Affixus Hip Fracture Nail, RH 125 DEG 11MM X 440MM
Zimmer Biomet, Inc.
Affixus Hip Fracture Nail, LH 130 DEG 11MM X 340MM
Zimmer Biomet, Inc.
Affixus Hip Fracture Nail, LH 130 DEG 11MM X 400MM
Zimmer Biomet, Inc.
Hemosphere System with the following three components: HEM1 Advanced Monitor, HEMSGM10 (Swan-Ganz Module), and HEMOXSC100 (Oximetry Smart Cable). …
Edwards Lifesciences, LLC
Affixus Hip Fracture Nail, RH 125 DEG 9MM X 320MM
Zimmer Biomet, Inc.
Metrotom 800 (130kV CT scanner) Industrial CT scanner for measuring and inspecting complete components made of plastic or light metal.
Carl Zeiss Metrology Inc
Affixus Hip Fracture Nail, LH 130 DEG 9MM X 400MM
Zimmer Biomet, Inc.
Affixus Hip Fracture Nail, RH 130 DEG 9MM X 340MM
Zimmer Biomet, Inc.
Affixus Hip Fracture Nail, RH 130 DEG 9MM X 320MM
Zimmer Biomet, Inc.
Affixus Hip Fracture Nail, 130 DEG 9MM X 180MM
Zimmer Biomet, Inc.
bvi Beaver EdgeAhead Safety Knife, (a) Sideport MVR .90mm 20G, REF 370531 (b) Sideport Angled, .60mm (23G), REF 378233 Product Usage: Specialt…
Beaver-Visitec International Inc.
Affixus Hip Fracture Nail, RH 125 DEG 9MM X 460MM
Zimmer Biomet, Inc.
MA3320-PM Premium Adult - SYK Mistral-Air Premium Blankets. MODEL #: MA3302-PM. CATALOG #(s): MA3302-PM
Stryker Medical Division of Stryker Corporation
Affixus Hip Fracture Nail, RH 130 DEG 13MM X 440MM
Zimmer Biomet, Inc.
Affixus Hip Fracture Nail, RH 130 DEG 11MM X 360MM
Zimmer Biomet, Inc.
Affixus Hip Fracture Nail, LH 125 DEG 9MM X 380MM
Zimmer Biomet, Inc.
Affixus Hip Fracture Nail, LH 125 DEG 9MM X 440MM
Zimmer Biomet, Inc.
cobas e 411 Immunoassay Analyzer-Model/Catalog/Part number: 04775279001/04775279973 - cobas e 411 analyzer (disk system) and 04775201001/04775201973 …
Roche Diagnostics Corporation
Affixus Hip Fracture Nail, 130 DEG 11MM X 180MM
Zimmer Biomet, Inc.
Elements Obturation Unit (EOU) used with respective Buchanan Heat Pluggers Device is an endodontic root canal plugger. It is intended to be used…
Ormco/Sybronendo
Affixus Hip Fracture Nail, RH 125 DEG 11MM X 460MM
Zimmer Biomet, Inc.
10 ML REAGENT CUP, B1034626, SAP 1221034626 for use with ABX PENTRA 400 / PENTRA C400
Horiba Instruments, Inc dba Horiba Medical
Affixus Hip Fracture Nail, RH 130 DEG 9MM X 260MM
Zimmer Biomet, Inc.
Affixus Hip Fracture Nail, LH 130 DEG 9MM X 300MM
Zimmer Biomet, Inc.
Affixus Hip Fracture Nail, RH 130 DEG 11MM X 380MM
Zimmer Biomet, Inc.
Affixus Hip Fracture Nail, RH 125 DEG 9MM X 260MM
Zimmer Biomet, Inc.
Affixus Hip Fracture Nail, LH 130 DEG 13MM X 460MM
Zimmer Biomet, Inc.
Affixus Hip Fracture Nail, LH 130 DEG 11MM X 460MM
Zimmer Biomet, Inc.
Affixus Hip Fracture Nail, RH 125 DEG 9MM X 400MM
Zimmer Biomet, Inc.
Affixus Hip Fracture Nail, LH 125 DEG 11MM X 440MM
Zimmer Biomet, Inc.
Affixus Hip Fracture Nail, RH 130 DEG 9MM X 380MM
Zimmer Biomet, Inc.
bvi Beaver Safety Sideport Knife: (a) 1.0mm, 45o, REF 378210 (b) 1.2mm, 45o, REF 378212 (c) 115mm, 45o, REF 378231 Product Usage: Specialty bl…
Beaver-Visitec International Inc.
Roche / Hitachi MODULAR Analyzer Systems-Immunoassay Analyzer-Model/Catalog/Part Number: 11568248001/11568248692 - Elecsys 2010 analyzer (disk system…
Roche Diagnostics Corporation
Affixus Hip Fracture Nail, RH 130 DEG 11MM X 280MM
Zimmer Biomet, Inc.
Affixus Hip Fracture Nail, LH 125 DEG 9MM X 340MM
Zimmer Biomet, Inc.
BARD UROS AUTOMATED URINE OUPTUT AND TEMPERATURE MONITOR, MODEL BK10001M The Uros(TM) Automated Urine Output and Temperature Monitor is indicated…
C.R. Bard, Inc.
Affixus Hip Fracture Nail, RH 130 DEG 9MM X 440MM
Zimmer Biomet, Inc.
Affixus Hip Fracture Nail, RH 130 DEG 11MM X 420MM
Zimmer Biomet, Inc.
Affixus Hip Fracture Nail, RH 125 DEG 13MM X 320MM
Zimmer Biomet, Inc.
Affixus Hip Fracture Nail, LH 130 DEG 11MM X 280MM
Zimmer Biomet, Inc.
Affixus Hip Fracture Nail, RH 125 DEG 9MM X 440MM
Zimmer Biomet, Inc.
Hemofiltration Standard Pack including BC 60 Plus-T 8036. Part Number: 701066990. Used in extracorporeal circulation during cardiopulmonary bypas…
Maquet
Empty IntraVia Container with Non-DEHP Fluid Path, 500mL Containers are intended for use in the preparation and administration of drug admixtures.
Baxter Healthcare Corporation
SST TWIST DRILL, STANDARD, 1.6mm Dia. x 127mm, REF 8054-010, STERILE This product line is intended for use in orthopaedic surgery (large and small…
MicroAire Surgical Instruments, LLC
Affixus Hip Fracture Nail, RH 130 DEG 9MM X 360MM
Zimmer Biomet, Inc.
Affixus Hip Fracture Nail, LH 125 DEG 11MM X 320MM
Zimmer Biomet, Inc.
Affixus Hip Fracture Nail, LH 130 DEG 9MM X 320MM
Zimmer Biomet, Inc.
Affixus Hip Fracture Nail, RH 130 DEG 11MM X 400MM
Zimmer Biomet, Inc.
Affixus Hip Fracture Nail, RH 130 DEG 13MM X 460MM
Zimmer Biomet, Inc.
Nearby Agencies
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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.