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 220 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 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 Aug 31, 2022 to Sep 14, 2022, covering 27 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).
Philips OmniLab Advanced+ Intl (Flow Gen), Rx Only. To provide noninvasive ventilation support for patients with obstructive sleep apnea syndrome (O…
Philips Respironics, Inc.
Various neurology packs
American Contract Systems, Inc.
Various Pacemaker Packs, Cardio Thoracic Packs
American Contract Systems, Inc.
Philips OmniLab Advanced + with Heated Tube Humidifier, Rx Only. To provide noninvasive ventilation support for patients with obstructive sleep apne…
Philips Respironics, Inc.
Orthex External Fixation Wire Sharp Bayonet 1.8 x 400 mm Model: K400-18BN
OrthoPediatrics Corp
Medline CHEST TUBE REORDER NO: DYNJ36762A
Medline Industries Inc.
Various ENT Packs
American Contract Systems, Inc.
VITROS XT 3400 Chemistry System with Version 3.7.2 and below Product Code: 6844458
Ortho-Clinical Diagnostics, Inc.
Insertion Kit for use with SENSATION PLUS 8F. 50cc Intra-Aortic Balloon Catheter
Datascope Corporation
Various Angiography/Cath Lab packs/trays
American Contract Systems, Inc.
Philips BiPAP A40, Rx Only. To provide noninvasive ventilation support for patients with obstructive sleep apnea syndrome (OSA) and respiratory insu…
Philips Respironics, Inc.
Abbott Alinity m SARS-CoV-2 CTRL Kit, REF 09N78-085, each kit contains 12 x 1.3mL CTRL - and 12 x 1.3 mL CTRL +, For In Vitro Diagnostic Use.
Abbott Molecular, Inc.
Various Cysto Packs
American Contract Systems, Inc.
Various hysterectomy, vaginal packs
American Contract Systems, Inc.
CARTO VIZIGO 8.5F Bi-Directional Guiding Sheath, REF: D138501. Used to introduce various cardiovascular catheters into the heart.
Biosense Webster, Inc.
Philips OmniLab Advanced+, Rx Only. To provide noninvasive ventilation support for patients with obstructive sleep apnea syndrome (OSA) and respirat…
Philips Respironics, Inc.
Optima Coil System Model OPTI0520CSF10. For endovascular embolization.
BALT USA, LLC
Various Laparoscopy Packs
American Contract Systems, Inc.
Various PICC Line, Central Line Packs
American Contract Systems, Inc.
Aesculap ENNOVATE SET SCREW STERILE-implants are used for dorsal monosegmental and multisegmental stabilization of the lumbar, thoracic and sacral sp…
Aesculap Implant Systems LLC
Pentacam AXL REF 70100, Pentacam HR REF 70900. Used to image the anterior segment of the eye.
Oculus Optikgeraete GMBH
DeRoyal Sterile Custom Kits containing ICU Medical MicroClave Clear Connectors
DeRoyal Industries Inc
Artis icono biplane- Model No. 11327600 Artis icono floor- Model No. 11327700
Siemens Medical Solutions USA, Inc
ARCHITECT STAT Troponin-I Reagent Kit, REF 2K41-27
Abbott Laboratories
VITEK 2 / MYLA VITEK 2 Software versions 8.01, 8.02 (veterinary use only), 9.01, 9.02, 9.03 MYLA Software versions V4.8 and V4.9
bioMerieux, Inc.
T-Cell Xtend REF TTK.610 US
OXFORD IMMUNOTEC LTD
The PRM is intended to be used as part of the ZOOM LATITUDE Programming System to communicate with Boston Scientific implantable pulse generators. Th…
Boston Scientific Corporation
Dimension Vista LOCI CA 15-3 Flex reagent cartridge. In Vitro Diagnostic for the quantitative measurement of CA 15-3. Siemens Material Number (SMN…
Siemens Healthcare Diagnostics, Inc.
FGFR RGQ RT-PCR Kit (RUO, not IVD) REF 8747010
Qiagen Sciences LLC
DigitalDiagnost C50 1.1
Philips North America Llc
AggreGuide A-100 Instrument
Aggredyne, Inc.
T-SPOT.TB REF TB.300 US
OXFORD IMMUNOTEC LTD
INFX-8000V. For radiographic and fluoroscopic studies and intervention.
Canon Medical System, USA, INC.
Metalogix Self-Drill Half-Pin, a component of the Revolution External Fixation System. Orthopedic. Metalogix Self-Drill Half-Pin 5x30x215mm RE…
New Standard Device Inc
NIM EMG Endotracheal Tube, Part Numbers: a) REF 8229308 b) REF 8229307 c) REF 8229306
Medtronic Xomed, Inc.
therascreen FGFR RGQ RT-PCR Kit (CE IVD, not sold in the US) REF 874711
Qiagen Sciences LLC
NIM CONTACT EMG Endotracheal Tube, Part Numbers: a) REF 8229508 b) REF 8229507 c) REF 8229506
Medtronic Xomed, Inc.
Pentacam AXL Wave REF 70020. Used to image the anterior segment of the eye.
Oculus Optikgeraete GMBH
AIM-V Medium REF AV.200/500
OXFORD IMMUNOTEC LTD
Artis Q floor- Model No. 10848280 Artis Q ceiling- Model No. 10848281 Artis Q biplane- Model No. 10848282 Artis Q zeego- Model No. 10848283 Artis…
Siemens Medical Solutions USA, Inc
Artis pheno- Model No. 10849000
Siemens Medical Solutions USA, Inc
Pentacam HR REF 70900. Used to image the anterior segment of the eye.
Oculus Optikgeraete GMBH
The PRM is intended to be used as part of the ZOOM LATITUDE Programming System to communicate with Boston Scientific implantable pulse generators. Th…
Boston Scientific Corporation
therascreen FGFR RGQ RT-PCR kit (US IVD) REF 874721
Qiagen Sciences LLC
NIM EMG Endotracheal Tube, Part Numbers: a) REF 8229307J b) REF 8229308J c) REF 8229306J
Medtronic Xomed, Inc.
The Programmer/Recorder/Monitor (PRM) is intended to be used as part of the ZOOM LATITUDE Programming System to communicate with Boston Scientific im…
Boston Scientific Corporation
TaperFit Stem, Size 0, 38mm OFFSET, 12/14 Taper + 188.550 Centraliser, For Cemented Use, REF 588.3800. Orthopedic hip implant component.
Corin Ltd
EverFlex Self-Expanding Peripheral Stent with Entrust Delivery System
Medtronic Inc.
a. Rapid Test Kit Coag-Sense Professional Blood Coagulation Test Prothrombin Time Test (PT/INR) Whole Blood Sample 50 Tests-IVD. Part No. 0356-50. …
Mckesson Medical-Surgical Inc. Corporate Office
FISHER SCIENTIFIC Fisherbrand SWAB, ROUND BOTTOM CLR (50/PK)FSHSCI Catalog # 1490712
Mckesson Medical-Surgical Inc. Corporate Office
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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.