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 157 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 2 critical (Class I-equivalent) actions, 48 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 Nov 15, 2023 to Nov 29, 2023, covering 20 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).
Compress Device Short Anchor Plug, 23 MM-For Correction of revision of unsuccessful osteotomy, arthrodesis, or previous joint replacement. Item Numb…
Biomet, Inc.
Compress Device Short Anchor Plug, 20 MM-For Correction of revision of unsuccessful osteotomy, arthrodesis, or previous joint replacement. Item Numb…
Biomet, Inc.
Mobile airway scope-diagnosis and observation to access airway anatomy, endotracheal/endobronchial intubation and management. Model Numbers: MAF-DM2…
Aizu Olympus Co., Ltd.
Hysteroscope-For endoscopic diagnosis within the uterus Model Number: HYF-1T.
Aizu Olympus Co., Ltd.
Compress Device Segmental Anchor Plug, 22 MM-For Correction of revision of unsuccessful osteotomy, arthrodesis, or previous joint replacement. Item …
Biomet, Inc.
Intera 1.5T Power/Pulsar
Philips North America Llc
Intera 1.5T
Philips North America Llc
FilmArray TORCH REF HTFA-ASY-0104. HTFA-ASY-0104 is the BIOFIRE TORCH Base which includes barcode scanner, touch screen computer and USB ports. T…
BioFire Diagnostics, LLC
Compress Device Segmental Anchor Plug, 16 MM-For Correction of revision of unsuccessful osteotomy, arthrodesis, or previous joint replacement. Item …
Biomet, Inc.
Compress Device Short Anchor Plug, 18 MM-For Correction of revision of unsuccessful osteotomy, arthrodesis, or previous joint replacement. Item Numb…
Biomet, Inc.
VariSoft infusion set, Model Number 1002830
Unomedical A/S
Alinity c Iron Reagent, Reference Number 08P3920
Sentinel CH SpA
GEM Premier 3000 PAK - pH, pCO2, pO2, Hct, Na+, K+, Ca++, Glucose and Lactate, Part Numbers 00024315009, 00024330009, 00024345009, 00024360009
Instrumentation Laboratory
Model 97745 Controller used with Models 97715 and 97716 Intellis Neurostimulators
Medtronic Neuromodulation
Compress Device Segmental Anchor Plug, 24 MM-For Correction of revision of unsuccessful osteotomy, arthrodesis, or previous joint replacement. Item …
Biomet, Inc.
Ventlab, LLC RescuMed manual resuscitators with integrated manometer, multiple accessory configurations to include: 1. RescuMed Adult Resuscitator…
SunMed Holdings, LLC
AVANOS BALLARD Closed Suction System for Adults, 14 Fr, DSE, MDI, Product code 221038, provide suction on patients on mechanical ventilation
Avanos Medical, Inc.
Uretero-reno fiberscope-For endoscopic diagnosis and treatment within the ureter and kidney. Model Numbers: URF-P7, URF-P7R, URF-V2, URF-V2R, URF-…
Aizu Olympus Co., Ltd.
Express Dry Seal Chest Drains (Express): 4000-100N DRAIN, EXPRESS, SINGLE; 4050-100N DRAIN, EXPRESS, BRU
Atrium Medical Corporation
Spectral CT on Rails, Software Version 5.1.0, Model Number 728334
Philips North America
LIFEPAK 15, REF: 99577-000046, Part Number V15-2-000051
Physio-Control, Inc.
LIFEPAK 15, REF: 99577-000061, Part Number V15-2-000067
Physio-Control, Inc.
Brilliance CT Big Bore with software version V4.8.0.10421 Model:728244 CT scanner and simulator designed for radiation oncology and therapy.
Philips North America Llc
LIFEPAK 15, REF: 99577-001957, Part Number V15-5-000586 and V15-7-000022
Physio-Control, Inc.
Big Bore RT with software version V4.8.0.10421- Model: 728242 CT scanner and simulator designed for radiation oncology and therapy.
Philips North America Llc
Regard CV PK, Item Numbers a) 880289014, b) 880289015; cardiovascular convenience kit
ROi CPS LLC
KWIKSTIK, P. venetum, Catalog numbers: a) 0794P (2-pack), b) 0794K (6-pack)
Microbiologics Inc
Ocean Water Seal Chest Drains (Ocean): Products REF Number Product Name (1)2002-000 DRAIN, OCEAN SINGLE W/AC,S; (2)2002-040 DRAIN, OCEAN SINGLE,…
Atrium Medical Corporation
LIFEPAK 15, REF: 99577-001960, Part Number: V15-7-000026
Physio-Control, Inc.
ADLT BLOOD CULTURE COLLECT KIT, REF DYNDH1245
MEDLINE INDUSTRIES, LP - Northfield
PERIPHERAL BLOOD CULTURE DRAW, REF DYNDH1561
MEDLINE INDUSTRIES, LP - Northfield
LIFEPAK 15, REF: 99577-001373, Part Number V15-7-000002
Physio-Control, Inc.
BLOOD CULTURE KIT, REF DYNDH1647B
MEDLINE INDUSTRIES, LP - Northfield
Oasis Dry Suction Water Seal Chest Drains (Oasis): (1)3600-100 DRAIN, OASIS SINGLE W/AC; (2)3612-100 DRAIN, OASIS PEDI A/C; (3)3650-100 DRAIN, OAS…
Atrium Medical Corporation
Spectral CT on Rails, Software Version 5.1.0, Model Number 728334
Philips North America
LIFEPAK 15, REF: 99577-001956, Part Number V15-7-000021
Physio-Control, Inc.
LIFEPAK 15, REF: 99577-001255, Part Number V15-2-001602
Physio-Control, Inc.
Mobilett Mira wireless (VA20) mobile x-ray system(s)
Siemens Medical Solutions USA, Inc
Atrium Advanta V12 Covered Stent System, 10mm x 59mm x 80cm (OUS)-Indicated for restoring and improving the patency of the iliac andrenal arteries. …
Atrium Medical Corporation
IBA Proton Therapy System - PROTEUS 235. PTS-11 versions, PTS-12 versions with Orion PPS version OSS6.0. Configured with Orion Patient Positioning Sy…
Ion Beam Applications S.A.
LIFEPAK 15, REF: 99577-000055, Part Number V15-2-000061
Physio-Control, Inc.
24 BLOOD CULTURE KIT, REF DYNDH1632
MEDLINE INDUSTRIES, LP - Northfield
LIFEPAK 15, REF: 99577-001958, Part Number: V15-7-000023
Physio-Control, Inc.
AU/DxC AU Chemistry Transferrin REF: OSR6152 Immune complexes formed in solution scatter light in proportion to their size, shape and concentration.…
Beckman Coulter Biomedical Division
LYFO-DISK, P. venetum, Catalog number 0794L
Microbiologics Inc
LIFEPAK 15, REF: 99577-001955, Part Number V15-5-000584 and V15-7-000020
Physio-Control, Inc.
CENTRAL LINE BLOOD CULTURE DRA, REF DYNDH1562
MEDLINE INDUSTRIES, LP - Northfield
Brilliance CT Big Bore Oncology with software version V4.8.0.10421 Model:728243 CT scanner and simulator designed for radiation oncology and ther…
Philips North America Llc
DigitalDiagnost 4 Chest/Emergency, used to acquire, process, store, display and export digital radiographic images.
Philips North America Llc
EVIS EXERA III BRONCHOVIDEOSCOPE OLYMPUS Model Number BF-P190
Olympus Corporation of the Americas
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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.