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 239 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 6 critical (Class I-equivalent) actions, 44 moderate recalls, and 0 lower-severity notices. Approximately 50 of 50 entries name a specific recalling firm, while 40 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 9, 2022 to Mar 16, 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).
Nextra CH Cannulated Hammertoe Mini Instrument Kit-indicated for small bone reconstruction limited to inter-digital repair and fusion of the lesser t…
Nextremity Solutions
RayStation/RayPlan- designed for treatment planning and analysis of radiation therapy. Software Version: 6.0.0.24 , 6.1.0.26 , 6.1.1.2 , 6.2.0.7…
RAYSEARCH LABORATORIES AB
CIRRUS HD-OCT, Models 5000 AngioPlex and 6000 AngioPlex
Carl Zeiss Meditec, Inc.
PuraSinus Absorbable Nasal Hemostat, Part Numbers 651-006
3-D Matrix, Inc.
ProteusPLUS and ProteusONE- designed to produce and deliver a proton beam for the treatment of patients with localized tumors and other conditions su…
Ion Beam Applications S.A.
NIM TRIVANTAGE EMG Endotracheal Tube
Medtronic Xomed, Inc.
Nextra Cannulated Hammertoe Standard Instrument Kit-indicated for small bone reconstruction limited to inter-digital repair and fusion of the lesser …
Nextremity Solutions
LuSys 2nd Generation of COVID-19 Viral Antigen Test For all mutant variety Cat: I-114(Saliva Test)
Lusys Laboratories, Inc.
HEMASHIELD GOLD KNITTED MICROVEL DOUBLE VELOUR VASCULAR GRAFT- D: 7 mm; L: 60 cm Indicated for use in the replacement or repair of arteries affecte…
Maquet Cardiovascular, LLC
COVID-19 IgG/IGM Antibody Test For Detection of COVID-19 IgG and IgM antibodies Catalog No: I-111
Lusys Laboratories, Inc.
Titanium MPJ (Toe Implant) TOE JOINT TITANIUM PC M/L, Part ID 17037
BioPro, Inc.
KWIK-STIK, Quality control kit for culture media, sold as: KWIK-STIK (single-pack) Enterococcus faecalis derived from ATCC 51299
Microbiologics Inc
Titanium MPJ (Toe Implant) TOE JOINT TITANIUM NPC MD, Part ID 16814
BioPro, Inc.
Microbiologics QC Sets and Panels: Helix Elite. Extended Enteric Bacterial Verification Panel (Inactivated Pellet) includes 21 pellets each comprised…
Microbiologics Inc
Everest MI XT Inner Dilator, Catalog Number 5101-90167
K2M, Inc
Philips Respironics V60 Plus Ventilator Part Number 1138747
Respironics California, LLC
Acorn 130 Stairlift, Brooks 130 Stairlift, Acorn 180 Stairlift, and Acorn Outdoor Stairlift
Acorn Stairlifts, Inc
QC Sets and Panels: KWIK-STIK Cepheid Smart GBS QC Set (Live Culture). Sets include: 1. 0864E4 Streptococcus agalactiae (Group B, lb) derived from…
Microbiologics Inc
Titanium MPJ (Toe Implant)TOE JOINT TITANIUM NPC LG, Part ID 16816
BioPro, Inc.
The DARCO¿ Locking Bone Plate System is designed with rhombus (parallelogram) plates of biocompatible titanium. The plates use either 2.7mm or 3.5m…
Wright Medical Technology, Inc.
Titanium MPJ (Toe Implant) TOE JOINT TITANIUM PC MS, Part ID 17197
BioPro, Inc.
da Vinci Xi and X 12-8 mm Conductive Cannula Reducer, REF: 470381-11
Intuitive Surgical, Inc.
Philips Respironics V60 Ventilator Part Number 1053617
Respironics California, LLC
MEDLINE Micro-Kill Bleach Germicidal Bleach Wipes
MEDLINE INDUSTRIES, LP - Northfield
Alinity m Integrated Reaction Units (IRU)
Abbott Molecular, Inc.
Digital Angiography System Bransist safire Generator Model D150GC-40
Shimadzu Medical Systems
Helix Elite" Molecular Standards: Inactivated Standard. Inactivated Neisseria gonorrhoeae Strain GL0071.
Microbiologics Inc
Collagen Plugs, CP3, 0.3mm, CP4, 0.4mm, CP5, 0.5 mm, Sterile, EO, Rx Only, CE Dry eye treatment
Lacrimedics Inc
BUTLER Clear Dip, 12 bottles/case
Sunstar Americas, Inc.
Bronchial Microbiology Brush, Catalog Number 4310 and 4320. Microbial sampling is performed by compressing a spring as the base of brush wire to expo…
Hobbs Medical, Inc.
Titanium MPJ (Toe Implant) TOE JOINT TITANIUM NPC SM, Part ID 16813
BioPro, Inc.
Helix Elite" Molecular Standards: Inactivated Standard. Inactivated Respiratory Syncytial Virus A Strain Long. Target pathogens are lyophilized …
Microbiologics Inc
Regard, TOTAL HIP - SPRINGFIELD, Item No. 8800297010, Case Quantity: 2, Sterile
ROi CPS LLC
KWIK-STIK, Quality control kit for culture media, sold as: a. KWIK-STIK 2-pack Enterococcus faecalis derived from ATCC 51299 b. KWIK-STIK 6-pa…
Microbiologics Inc
Celltrion DiaTrust COVID-19 Ag Rapid Test, Reference No. CT-P60 D-2 02
CELLTRION USA INC
QC Sets and Panels: KWIK-STIK. Cepheid Xpert GBS QC Set (Live Culture). Sets include: 1. 0864E3 Streptococcus agalactiae (Group B, lb) derived fro…
Microbiologics Inc
Celltrion DiaTrust COVID-19 Ag Rapid Test, Reference No. CT-P60 D-2 02
CELLTRION USA INC
AU/DxC AU Magnesium, Catalog/REF Number OSR6189, UDI 15099590010850
Beckman Coulter Inc.
Titanium MPJ (Toe Implant) TOE JOINT TITANIUM PC LG, Part ID 17038
BioPro, Inc.
Titanium MPJ (Toe Implant)TOE JOINT TITANIUM PC SM, Part ID 17035
BioPro, Inc.
Titanium MPJ (Toe Implant) TOE JOINT TITANIUM NPC ML, Part ID 16815
BioPro, Inc.
Everest MI XT Outer Dilator, Catalog Number 5101-90168
K2M, Inc
Titanium MPJ (Toe Implant) TOE JOINT TITANIUM NPC MS, Part ID 17198
BioPro, Inc.
Microbiologics QC Sets and Panels. BD MAX" CT/GC/TV Verification and Control Panel. Containing High, Medium and Low Level Controls.
Microbiologics Inc
OPAQUE Herrick Lacrimal Plugs, HP3, 0.3 mm, HP5, 0.5mm, HP7, 0.7.mm, STERILE, EO, Rx only, CE Dry eye treatment
Lacrimedics Inc
Brasseler USA, K-WIRE, Double Trocar Smooth, REF KM172-26-35S
Brasseler USA, Medical L.L.C.
Titanium MPJ (Toe Implant) TOE JOINT TITANIUM PC MD, Part ID 17036
BioPro, Inc.
NavitrackER Kit A: Knee, Model Number 20-8000-000-07,
Orthosoft, Inc. dba Zimmer CAS
LYFO-DISK, Quality control kit for culture media, sold as: LYFO-DISK Enterococcus faecalis derived from ATCC 51299
Microbiologics Inc
MEDPOR Titan OFW - MTB - Right - 1.0mm, Catalog number 81032
Stryker Leibinger GmbH & Co. KG
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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.