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 480 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 1 critical (Class I-equivalent) actions, 49 moderate recalls, and 0 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 Jan 31, 2018 to Feb 7, 2018, covering 17 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).
Triage Drugs of Abuse Plus TCA 25 Test Kit, Model Numbers 92000, 92590, 92591; 25 individually pouched devices, 1 bottle of Wash Solution, 1 Pipette…
Alere San Diego, Inc.
Affixus Hip Fracture Nail, RH 130 DEG 11MM X 260MM
Zimmer Biomet, Inc.
Affixus Hip Fracture Nail, LH 130 DEG 11MM X 260MM
Zimmer Biomet, Inc.
Affixus Hip Fracture Nail, 125 DEG 9MM X 180MM
Zimmer Biomet, Inc.
Affixus Hip Fracture Nail, LH 130 DEG 9MM X 440MM
Zimmer Biomet, Inc.
Affixus Hip Fracture Nail, LH 130 DEG 9MM X 420MM
Zimmer Biomet, Inc.
Graseby 3300 Pump and Graseby 3000 Series Pump Accessories Patient controlled syringe pump. Use for Infusion
Smiths Medical ASD Inc.
Affixus Hip Fracture Nail, RH 130 DEG 9MM X 400MM
Zimmer Biomet, Inc.
Affixus Hip Fracture Nail, RH 130 DEG 11MM X 320MM
Zimmer Biomet, Inc.
Affixus Hip Fracture Nail, LH 130 DEG 11MM X 300MM
Zimmer Biomet, Inc.
Affixus Hip Fracture Nail, LH 130 DEG 9MM X 340MM
Zimmer Biomet, Inc.
Affixus Hip Fracture Nail, RH 130 DEG 13MM X 280MM
Zimmer Biomet, Inc.
Affixus Hip Fracture Nail, RH 130 DEG 9MM X 300MM
Zimmer Biomet, Inc.
Affixus Hip Fracture Nail, RH 130 DEG 11MM X 340MM
Zimmer Biomet, Inc.
Affixus Hip Fracture Nail, RH 125 DEG 11MM X 380MM
Zimmer Biomet, Inc.
Affixus Hip Fracture Nail, RH 130 DEG 11MM X 300MM
Zimmer Biomet, Inc.
Affixus Hip Fracture Nail, RH 125 DEG 9MM X 420MM
Zimmer Biomet, Inc.
Affixus Hip Fracture Nail, RH 125 DEG 9MM X 340MM
Zimmer Biomet, Inc.
GE HEALTHCARE CARESCAPE Central Station (CSCS) software version 2.0.2 The CARESCAPE Central Station is intended to collect information from a ne…
GE Medical Systems Information Technologies, Inc.
Tosoh¿Automated Enzyme Immunoassay Analyzer AIA-900, Product Catalog No. 022930. Product Usage: The AIA-900 Automated Enzyme Immunoassay System is …
Tosoh Bioscience Inc
bvi Beaver Xstar Safety Crescent, 2.5mm, 55o Bevel Up, REF 378234 Product Usage: Specialty blades and knives are used for stab and cut incision…
Beaver-Visitec International Inc.
Affixus Hip Fracture Nail, LH 130 DEG 11MM X 440MM
Zimmer Biomet, Inc.
9x15" Medium Utility Positioner with Cover
Molnlycke Health Care, Inc
Equinoxe Cage, Glenoid, Alpha, Small Product Usage: The Equinoxe Shoulder System is indicated for use in skeletally mature individuals with degen…
Exactech, Inc.
Affixus Hip Fracture Nail, RH 125 DEG 9MM X 360MM
Zimmer Biomet, Inc.
Affixus Hip Fracture Nail, LH 125 DEG 9MM X 260MM
Zimmer Biomet, Inc.
Affixus Hip Fracture Nail, RH 125 DEG 11MM X 300MM
Zimmer Biomet, Inc.
Affixus Hip Fracture Nail, RH 130 DEG 9MM X 420MM
Zimmer Biomet, Inc.
Equinoxe Cage, Glenoid, Alpha, Medium Product Usage: The Equinoxe Shoulder System is indicated for use in skeletally mature individuals with dege…
Exactech, Inc.
Affixus Hip Fracture Nail, LH 130 DEG 11MM X 380MM
Zimmer Biomet, Inc.
15 ML REAGENT CUP, B1037307, SAP 1221037307 for use with ABX PENTRA 400 / PENTRA C400
Horiba Instruments, Inc dba Horiba Medical
Affixus Hip Fracture Nail, RH 130 DEG 13MM X 300MM
Zimmer Biomet, Inc.
Tosoh¿Sorter 9tray, Product Code 022931and Tosoh¿Sorter 19tray, Product Code 022932. Product Usage: The AIA-900 9tray Sorter and AIA-900 19tray S…
Tosoh Bioscience Inc
bvi Beaver Optimum Safety Sideport Knife: (a) Straight 15o, REF 378235 (b) Straight 22.5o, REF 378236 (c) Straight 30o, REF 378237 (d) Straig…
Beaver-Visitec International Inc.
Affixus Hip Fracture Nail, LH 130 DEG 9MM X 280MM
Zimmer Biomet, Inc.
Affixus Hip Fracture Nail, RH 125 DEG 13MM X 260MM
Zimmer Biomet, Inc.
Affixus Hip Fracture Nail, LH 130 DEG 11MM X 420MM
Zimmer Biomet, Inc.
7x10" Small Utility Positioner with Cover
Molnlycke Health Care, Inc
bvi Beaver Xstar Safety Slit Knife: (a) REF 378214, 1.4mm, 45o Bevel Up (b) REF 378215, 1.50mm, 45o Bevel Up (c) REF 378217, 1.7mm, 45o Bevel Up…
Beaver-Visitec International Inc.
PURE OXYGEN CONCENTRATOR, CHAD Drive, Models CH5000 and CH5000S
Inovo, Inc
MyCareLink Smart Patient Monitors. It is intended for use with a compatible Medtronic patient implanted heart device. The reader is a portable ele…
Medtronic Inc., Cardiac Rhythm and Heart Failure
Brilliance iCT - Model 728306 Computed Tomography X-ray systems
Philips Medical Systems (Cleveland) Inc
smith&nephew Mini-Fragment Plating System, VLP(R) Mini-Mod Small Bone Plating System, EVOS(R) Mini Plating system, 2.0MM STOUT STRAIGHT PLATE, 8 HOLE…
Smith & Nephew, Inc.
Adult AirLife dual-limb, dual-heat circuit (Model AH280) with AirLife Humidification Chamber, Model Number AH290. The AH290 Humidification Chamber…
Vyaire Medical
MyCareLink Patient Monitors. It is intended for used with a compatible Medtronic patient implanted heart device. The monitor is an external electr…
Medtronic Inc., Cardiac Rhythm and Heart Failure
Measurement Specialties Reusable Temperature Probe Autoclavable. Sold as Esophageal/Rectal (Adult), Esophageal/Rectal (Pediatric), and Skin (Adult) …
Measurement Specialties Inc
smith&nephew, 2.4 MM, 6 HOLE, EVOS, FLEX PLATE, SST Plate, REF CATALOG NUMBER 72442360N, NON-STERILE, Rx only, (01)00885556456446(10), (11)171116 …
Smith & Nephew, Inc.
MARS Treatment Kit, Use only with MARS(R) Monitor 1TC, GAMBRO, Product Code 800541
Baxter Healthcare Corporation
Radial Osteotome Blade, REF 71369314. Used for cutting or preparing bone.
Smith & Nephew, Inc.
CP5 Centrifugal Pump, made up of the drive unit, the emergency system and the pump control panel. It used with an Electrical Remote-Controlled (ERC)…
Sorin Group Deutschland GmbH
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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.