Medical device recalls
Device recalls are the largest single group in this archive, because the FDA logs corrections and removals as well as outright withdrawals. Many are handled entirely between the manufacturer and a hospital and need nothing from a patient. Each notice states who has to act.
13,634 stored notices, reported between Jun 20, 2012 and Sep 9, 2026. Newest first.
Reported Mar 9, 2022
Brasseler USA, K-WIRE, Double Trocar Smooth, REF KM172-26-35S
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Brasseler USA, Medical LLC
FDA (openFDA device enforcement)
Reported Mar 9, 2022
Celltrion DiaTrust COVID-19 Ag Rapid Test, Reference No. CT-P60 D-2 02
High riskUsing this product could cause serious injury, illness or death — stop using it now.Celltrion USA Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Mar 9, 2022
Bronchial Microbiology Brush, Catalog Number 4310 and 4320. Microbial sampling is performed by compressing a spring as…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hobbs Medical, Inc.
FDA (openFDA device enforcement)
Reported Mar 9, 2022
da Vinci Xi and X 12-8 mm Conductive Cannula Reducer, REF: 470381-11
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Intuitive Surgical, Inc.
FDA (openFDA device enforcement)
Reported Mar 9, 2022
Everest MI XT Inner Dilator, Catalog Number 5101-90167
Moderate riskThis product could cause temporary or reversible health problems — stop using it.K2M, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Mar 9, 2022
OPAQUE Herrick Lacrimal Plugs, HP3, 0.3 mm, HP5, 0.5mm, HP7, 0.7.mm, STERILE, EO, Rx only, CE Dry eye treatment
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Lacrimedics Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Mar 9, 2022
MEDLINE Micro-Kill Bleach Germicidal Bleach Wipes
Moderate riskThis product could cause temporary or reversible health problems — stop using it.MEDLINE INDUSTRIES, LP - Northfield
FDA (openFDA device enforcement)
Reported Mar 9, 2022
Microbiologics QC Sets and Panels: Helix Elite. Extended Enteric Bacterial Verification Panel (Inactivated Pellet)…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Microbiologics Inc.
9 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 9, 2022
NavitrackER Kit A: Knee, Model Number 20-8000-000-07,
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Orthosoft, Inc. dba Zimmer CAS
FDA (openFDA device enforcement)
Reported Mar 9, 2022
Philips Respironics V60 Ventilator Part Number 1053617
High riskUsing this product could cause serious injury, illness or death — stop using it now.Respironics California, LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Mar 9, 2022
Regard, TOTAL HIP - SPRINGFIELD, Item No. 8800297010, Case Quantity: 2, Sterile
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ROi CPS LLC
FDA (openFDA device enforcement)
Reported Mar 9, 2022
Digital Angiography System Bransist safire Generator Model D150GC-40
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Shimadzu Medical Systems
1 more product in this recall
FDA (openFDA device enforcement)
Reported Mar 9, 2022
MEDPOR Titan OFW - MTB - Right - 1.0mm, Catalog number 81032
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Leibinger GmbH & Co. KG
FDA (openFDA device enforcement)
Reported Mar 9, 2022
BUTLER Clear Dip, 12 bottles/case
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sunstar Americas, Inc.
FDA (openFDA device enforcement)
Reported Mar 9, 2022
The DARCO¿ Locking Bone Plate System is designed with rhombus (parallelogram) plates of biocompatible titanium. The…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Wright Medical Technology, Inc.
FDA (openFDA device enforcement)
Reported Mar 2, 2022
The Optima Coil System consists of an implantable embolization coil comprised of a platinum-tungsten alloy attached to…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Balt USA, LLC
FDA (openFDA device enforcement)
Reported Mar 2, 2022
BD Vacutainer Luer Lok Access Device - intended as a sterile, single use device designed to provide a connection to a…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Becton Dickinson & Company
FDA (openFDA device enforcement)
Reported Mar 2, 2022
Arcos Modular Revision Hip System, Standard Cone Prox Body, Porous Plasma,Size A, 60 MM Item Number: 11-301301
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Biomet, Inc.
7 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 2, 2022
BARD SURESTEP INTERMITTENT CATHETER TRAY, 14Fr, REF INTS14C
Moderate riskThis product could cause temporary or reversible health problems — stop using it.C.R. Bard Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Mar 2, 2022
DuraMatrix-Onlay Collagen Dura Substitute Membrane 4 inches x 5 inches (10.0cm x 12.5cm) REF: CDSLM45
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Collagen Matrix, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Mar 2, 2022
Michels Transport Medium, 20ML Prefilled Cont
Moderate riskThis product could cause temporary or reversible health problems — stop using it.MEDLINE INDUSTRIES, LP - Northfield
1 more product in this recall
FDA (openFDA device enforcement)
Reported Mar 2, 2022
Endurant, Endurant II and Endurant IIs Stent Graft System: Medtronic Endurant Stent Graft System Model/REF…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Vascular, Inc.
FDA (openFDA device enforcement)
Reported Mar 2, 2022
IPELA FHD PTZ TILE KITS with Axis cameras used in combination with Natus Neuroworks/Sleepworks software
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Natus Neurology dba Excel Tech., Ltd. (XLTEK)
FDA (openFDA device enforcement)
Reported Mar 2, 2022
NobelReplace Conical Connection RP 4.3x11.5 mm REF 36707 STERILE R
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nobel Biocare USA LLC
FDA (openFDA device enforcement)
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RecallNow is not a government agency. Every notice above was published by the FDA, USDA FSIS or CPSC and links back to its source. Browse the whole archive.