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 133 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 100,165 records spanning 1995 through the present, FDA Medical Devices accounts for roughly 39.0% 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 7 critical (Class I-equivalent) actions, 43 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 Apr 17, 2024 to Apr 24, 2024, covering 19 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).
Trocar Needle - Used for dilating puncture sites or catheter tracts for percutaneous placement of devices for vascular and non-vascular applications …
Cook Incorporated
MR 7700, Magnetic Resonance System.
Philips North America Llc
GYROSCAN T5, Magnetic Resonance System.
Philips North America Llc
Intera Achieva 1.5T Pulsar, Magnetic Resonance System.
Philips North America Llc
Achieva 3.0TX for PET, Magnetic Resonance System.
Philips North America Llc
Smiths Medical Medfusion Model 3500 Syringe pumps, Item Numbers: a) 3500 b) 3500-0600-00 c) 3500-0600-01 d) 3500-0600-249 e) 3500-0600-50 f) …
Smiths Medical ASD Inc.
Intera CV, Magnetic Resonance System.
Philips North America Llc
Trilogy Evo O2, all software versions except 1.05.06.00. Ventilator for pediatric and adult patients.
Philips Respironics, Inc.
Masimo Rad-G, Pulse Oximeter (W/Patient Cable), REF:9849, Rx Only,
Masimo Corporation
Siemens Artis Models: Interventional Fluoroscopic X-Ray Systems-Models: Artis zee floor- 10094135 Artis zee ceiling- 10094137 Artis zee multi-purp…
Siemens Medical Solutions USA, Inc
Achieva 1.5T Conversion, Magnetic Resonance System.
Philips North America Llc
Intera 1.5T R11, Magnetic Resonance System.
Philips North America Llc
Achieva 1.5T Initial, Magnetic Resonance System.
Philips North America Llc
Dilator - Coons Taper - Used for dilating puncture sites or catheter tracts for percutaneous placement of devices for vascular and non-vascular appli…
Cook Incorporated
Intera 1.0T Power/Pulsar, Magnetic Resonance System.
Philips North America Llc
Evolution Upgrade 3.0T, Magnetic Resonance System.
Philips North America Llc
RENASYS EDGE 300ML CANISTER WITH Solidifier- Indicated for patients who would benefit from a suction pump (NPWT), as it may promote wound healing. P…
Smith & Nephew Medical, Ltd.
SmartPath to dStream for 1.5T, Magnetic Resonance System.
Philips North America Llc
Achieva 3.0T for PET, Magnetic Resonance System.
Philips North America Llc
Elekta Disposable Biopsy Needle Kit for Leksell Stereotactic System, REF 911933, 2.1mm Diameter / 14 Gauge, containing 6 inner boxes labeled REF 9117…
Elekta Instrument AB
MR 5300, Magnetic Resonance System.
Philips North America Llc
Ingenia Ambition X, Magnetic Resonance System.
Philips North America Llc
Trilogy EV300, all software versions except 1.05.06.00. Ventilator for pediatric and adult patients.
Philips Respironics, Inc.
Intera 1.5T Power/Pulsar, Magnetic Resonance System.
Philips North America Llc
Garbin EVO, all software versions except 1.05.06.00. Ventilator for pediatric and adult patients. (sold outside US)
Philips Respironics, Inc.
Intera 0.5T Standard, Magnetic Resonance System.
Philips North America Llc
Trilogy Evo, all software versions except 1.05.06.00. Ventilator for pediatric and adult patients.
Philips Respironics, Inc.
CryoValve SG Cryopreserved Pulmonary Human Heart Valve
Artivion, Inc
SmartPath to dStream for XR and 3.0T, Magnetic Resonance System.
Philips North America Llc
Ingenia 1.5T, Magnetic Resonance System.
Philips North America Llc
Dr¿ger Perseus A500 Anesthesia Workstation
Draeger Medical, Inc.
Smiths Medical Model 3010 Syringe pumps: a. Protege Model 3010, b. Medfusion Model 3010A, c. Protege UK Model 3010E
Smiths Medical ASD Inc.
STRATAFIX Spiral MONOCRYL Plus Bidirectional Knotless Tissue Control Device: STRATAFIX SPIRAL MONOCRYL PLUS BI UD 12+12IN(30+30CM) USP3-0(M2) D/A PS …
Ethicon, Inc.
GYROSCAN T10-NT, Magnetic Resonance System.
Philips North America Llc
Intera 3.0T Quasar Dual, Magnetic Resonance System.
Philips North America Llc
Ingenia 3.0T, Magnetic Resonance System.
Philips North America Llc
Ingenia Ambition S, Magnetic Resonance System.
Philips North America Llc
Dilator With AQ Hydrophilic Coating - Intended to be used for dilating puncture sites or catheter tracts for percutaneous placement of devices for va…
Cook Incorporated
RENASYS EDGE 800ML CANISTER WITH Solidifier- Indicated for patients who would benefit from a suction pump (NPWT), as it may promote wound healing Pr…
Smith & Nephew Medical, Ltd.
Chiba Biopsy Needle - Used for aspiration biopsy. REFERENCE PART NUMBER (RPN) ORDER NUMBER (GPN): 1) DCHN-18-10.0 G01559 2) DCHN-18-10.0-U G05…
Cook Incorporated
SW Bari Lift & Transfer, Model Number 38060000
Raye's Inc.
Intera 1.5T Master/Nova, Magnetic Resonance System.
Philips North America Llc
Ingenia 3.0T CX, Magnetic Resonance System.
Philips North America Llc
EndoVive 20 Fr Safety PEG Push w/ENFit Kit (Box 2)-Indicated for enteral nutrition directly into the stomach in both pediatric and adult patients who…
Boston Scientific Corporation
LVP Software of the Ivenix Infusion System (IIS), Version 5.8.0.
Fresenius Kabi USA, LLC
EZ2 Connect MDx-IVD Designed to perform automated isolation and purification of nucleic acids in molecular diagnostic and/or molecular biology applic…
Qiagen Sciences LLC
ConvaTec CarboFlex, 15cm x 20cm, 6 in. x 8 in., Order No. 403204, Odor Control Dressing, Sterile. Packaged 1 dressing/immediate package, 5 packages/…
ConvaTec, Inc
Femoral Resurfacing Cup - (xx)MM, Ti-6AI-4V ELI, TiN CERAMIC W/ PLASMA SPRAY, STERILEEO, Reference Numbers: 01-03-0042 01-03-0044 01-03-0045 01-03-00…
Synovo Production
Chromophare Surgical Light System , REF CH00000001
Stryker Communications
Hillrom Welch Allyn Connex ProBP 3400 Digital Blood Pressure Device, marketed under the following models: a) PROBP 3400, SUREBP, BLUETOOTH, MOBILE…
Baxter Healthcare Corporation
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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
Read our methodology — how this data is sourced, computed, and verified.