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 138 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 3 critical (Class I-equivalent) actions, 47 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 Mar 13, 2024 to Mar 20, 2024, covering 21 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).
LVP software of the Ivenix Infusion System (IIS), LVP-SW-0004
Fresenius Kabi USA, LLC
SPII Model Lubinus, Long Stem Prosthesis XL Neck, cemented
Waldemar Link GmbH & Co. KG (Mfg Site)
BVI Visitec Irrigation Handle (20/SP)- Intended to be fit with a cannula for irrigation of the eye Catalog Number: 581012
Beaver Visitec International, Inc.
LVP software of the Ivenix Infusion System (IIS); LVP-SW-0004
Fresenius Kabi USA, LLC
L-Aneurysm Clip TITANIUM Paddle-Clip, permanent, 11 mm straight, Sterile
Peter Lazic Gmbh
CLEARLINK Non-DEHP Solution Set Luer Lock Adapter, Product Code 2R8401
Baxter Healthcare Corporation
CARTO VIZIGO Bi-Directional Guiding Sheath, REF D128502 The CARTO VIZIGOTM Bi-Directional Guiding Sheath is designed to provide accessibility and…
Biosense Webster, Inc.
CERENOVUS CEREBASE DA Guide Sheath, Part Numbers: a) GS9080SD; b) GS9090SD; c) GS9095SD; Vascular guide-catheter, single-use
Medos International Sarl
Atellica IM Erythropoietin (EPO) Assay (100 Test)
Siemens Healthcare Diagnostics, Inc.
SPII Model Lubinus, Long Stem Prosthesis Standard Neck, cemented
Waldemar Link GmbH & Co. KG (Mfg Site)
D-Clip Standard/Mini Applier, 230mm bayonet, jaw rigid, double action.
Peter Lazic Gmbh
EasyPoint Needle, 25G x 5/8", REF: 82091
Retractable Technologies, Inc.
D-Clip Standard/Mini Applier, 210mm bayonet, jaw rigid, double action.
Peter Lazic Gmbh
SPII Model Lubinus, Hip Prosthesis Stem Standard Neck, cemented
Waldemar Link GmbH & Co. KG (Mfg Site)
L-Aneurysm Clip TITANIUM Paddle-Clip, permanent, 11 mm straight, Non-Sterile
Peter Lazic Gmbh
ADVIA Centaur Erythropoietin (EPO) Assay (100 Test)
Siemens Healthcare Diagnostics, Inc.
SPII Model Lubinus, Hip Prosthesis Stem XL Neck, cemented
Waldemar Link GmbH & Co. KG (Mfg Site)
STERIS Boot Assembly, Traction Device, OT 1000, Part Number REF 10009192
Baxter Healthcare Corporation
CVS Health Waterproof Wound Tracking Dressing, REF CVS690330, immediate package contains 1 sterile dressing, 4 in. x 4 in., 4 dressings per box, 24 b…
MEDLINE INDUSTRIES, LP - Northfield
Shimadzu, Trinias, Digital Angiography System
SHIMADZU CORPORATION MEDICAL SYSTEMS DIVISION
D-Clip Standard/Mini Applier, 190mm bayonet, jaw rigid, double action.
Peter Lazic Gmbh
Opal, Intervertebral Cage, 10x32mm, h 11mm, Revolvable-Indicated for degenerative spine disease Part Number: 08.803.231S
Synthes (USA) Products LLC
Synapse PACS - Version 7.2.100
FUJIFILM Healthcare Americas Corporation
RAPIDSORB IPS Battery Pack, Sterile-Intended for use in non-load bearing fracture repair and reconstructive procedures of the craniofacial skeleton (…
Synthes (USA) Products LLC
Synapse PACS - Version 7.1.000
FUJIFILM Healthcare Americas Corporation
ConvaTec Natura Stomahesive Post-Operative / Surgical Ostomy System, REF 416938, 1 3/4 in. 45mm, Sterile.
ConvaTec, Inc
13 mm Titanium Hindfoot Arthrodesis Cannulated Nails EX, sterile -Intended to facilitate tibiotalocalcaneal arthrodesis to treat severe foot/ankle de…
Synthes (USA) Products LLC
BD Pyxis: MedStation ES, REF: 323; Anesthesia Station ES, REF: 327; MedStation ES Tower, REF: 352;
CareFusion 303, Inc.
VITROS 5600 Integrated System Catalog Nos. 6802413 (regular) and 6802915 (refurbished)
Ortho-Clinical Diagnostics, Inc.
Synapse PACS - Version 7.2.000
FUJIFILM Healthcare Americas Corporation
Invacare Homecare Series Bed and Invacare G-Series Beds Containing Component Model Numbers: (1) G50 (2) G53 (3) G54 (4) BAR5490IVC (5) BAR5000…
Invacare Corporation
DISP.HASSON TROCAR 10/110MM, Product Code EK230SU. For use in laparoscopic procedures.
Aesculap Inc
NO 4 TRIATHLON TS PLUS TIB INS X3 POLY 11 MM
Howmedica Osteonics Corp.
Synapse PACS - Version 7.1.000US
FUJIFILM Healthcare Americas Corporation
VITROS XT 7600 Integrated System, Catalog No. 6844461
Ortho-Clinical Diagnostics, Inc.
DISP.TROCAR W.DILATING PIN 12/110MM, Product Code EK234SU. For use in laparoscopic procedures.
Aesculap Inc
Embrace Drill Tower, Wedged (25mm)
Waldemar Link GmbH & Co. KG (Mfg Site)
X3 TRIATHLON CS INSERT NO 6 10 MM
Howmedica Osteonics Corp.
VITROS 5600 Integrated System (New and Refurbished)
Ortho-Clinical Diagnostics, Inc.
TFNA Femoral Nail 9mm, right, 130¿, L 235mm-Intended for temporary fixation and stabilization of proximal femur fractures. Part Number: 04.037.944S
Synthes (USA) Products LLC
MIC* Gastric-Jejunal Feeding Tube with ENFit Connectors: a) MIC* Gastric-Jejunal Feeding Tube Kit with ENFit Connector - Endoscopic/Radiologic P…
Avanos Medical, Inc.
MRI system: Vantage Elan, Model: MRT-2020
Canon Medical System, USA, INC.
DISP.TROCAR W.DILATING PIN 12/110MM, Product Code EK236SU. For use in laparoscopic procedures.
Aesculap Inc
1.5MM Drill Bit/QC/85MM Sterile-surgical, orthopedic, pneumatic powered & accessory/attachment Part Number: 310.15S
Synthes (USA) Products LLC
VITROS XT7600 Integrated System
Ortho-Clinical Diagnostics, Inc.
VITROS XT 3400 Chemistry System, Catalog No. 6844458
Ortho-Clinical Diagnostics, Inc.
VITROS 3600 Immunodiagnostic System (New and Refurbished)
Ortho-Clinical Diagnostics, Inc.
MIC* Gastric-Jejunal Feeding Tube, Endoscopic/Radiologic Placement, GJ-Tube: a) MIC* Gastric-Jejunal Feeding Tube Kit - Endoscopic/Radiologic Placem…
Avanos Medical, Inc.
X3 TRIATHLON CS INSERT NO 3 10 MM
Howmedica Osteonics Corp.
VA-LCP Clavicle Plate 2.7, shaft, CS1, right-Intended for fixation of clavicle bone fragments. Part Number: 02.112.621S
Synthes (USA) Products LLC
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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.