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 Feb 4, 2026
PearMatrix P-15 Peptide Enhanced Bone Graft Bone Graft, 1.0cc REF: 730-010
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cerapedics, Inc.
FDA (openFDA device enforcement)
Reported Feb 4, 2026
Brand Name: Elekta Medical Linear Accelerator Product Name: Elekta Synergy, Elekta Harmony, Elekta Infinity, Versa HD…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elekta, Inc.
FDA (openFDA device enforcement)
Reported Feb 4, 2026
Bandages and first aid kits: FIRST AID KIT 24/42PC, LUCKY FIRST AID BANDAGES 24CT
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Gold Star Distribution Inc.
4 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 4, 2026
Brand Name: LimFlow Vector Product Name: LimFlow Vector Model/Catalog Number: VT-US-23
Moderate riskThis product could cause temporary or reversible health problems — stop using it.LimFlow, Inc.
FDA (openFDA device enforcement)
Reported Feb 4, 2026
LSL Healthcare, Central Line Dressing Kit, Model/Catalog Number: 2519CP, medical procedure convenience kit
Moderate riskThis product could cause temporary or reversible health problems — stop using it.LSL Healthcare Inc.
FDA (openFDA device enforcement)
Reported Feb 4, 2026
Medline medical procedure convenience kits labeled as: NERVE BLOCK TRAY 2, Kit SKU DYNJRA2713
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medline Industries, LP
14 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 4, 2026
BEAR Implant. Model Number: 1000.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Miach Orthopaedics
FDA (openFDA device enforcement)
Reported Feb 4, 2026
Conductivity Standard Solution Catalog/Model Numbers: 10001, 10011, 10021, 10032, 10040, 10040c, and 10041 Conductivity…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.NIPRO Technical Services, Inc.
FDA (openFDA device enforcement)
Reported Feb 4, 2026
Evolution Upgrade 1.5T. Product Codes (REF): (1) 782148, (2) 782116. MR systems with SW version R11.1 and R12.1.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips North America
12 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 4, 2026
Interventional Fluoroscopic X-Ray System: LUMINOS Q.namix R; Siemens Material Number (SMN): 11574002; With Software…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Feb 4, 2026
Brand Name: Broselow Product Name: Broselow Pediatric Emergency Rainbow Tape Model/Catalog Number: 7700REA Software…
High riskUsing this product could cause serious injury, illness or death — stop using it now.SunMed Holdings, LLC
3 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 4, 2026
Brand Name: Zimmer Tourniquet Systems Product Name: A.T.S.¿ 5000TS Tourniquet Systems Model/Catalog Number: 60500010100…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer Surgical Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jan 28, 2026
SIGMA Spectrum Infusion Pump, Model/Catalog Number: 35700BAX2
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Baxter Healthcare Corporation
FDA (openFDA device enforcement)
Reported Jan 28, 2026
The LDL-Cholesterol assay is comprised of two distinct phases. In phase one a unique detergent solubilizes cholesterol…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter Ireland, Inc.
FDA (openFDA device enforcement)
Reported Jan 28, 2026
Rifton Equipment, TRAM. Model/Catalog Number: K310. The TRAM is a powered lift device for transferring clients in a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Community Products, LLC
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 28, 2026
Brand Name: EDAN Product Name: Fetal Monitor Model/Catalog Number: F2, F3 Product Description: The devices are bedside…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Edan Diagnostics
15 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 28, 2026
GE Healthcare Omni Legend, sold under the following names: OMNI Legend 16, Omni Legend 21, OMNI Legend 32, Omni Legend…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ge Medical Systems Israel, Functional Imaging
FDA (openFDA device enforcement)
Reported Jan 28, 2026
SQ40S Blood Transfusion Filter
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GVS TM, Inc.
FDA (openFDA device enforcement)
Reported Jan 28, 2026
Tego Connector: REF: 011-D1000, 01C-D1000, 055-D1000, D1000; Conector Tego: REF: LAT-D1000
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ICU Medical, Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 28, 2026
Brand Name: Ion Endoluminal System Product Name: Ion Vision Probe Bag Model/Catalog Number: 490127 Software Version:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Intuitive Surgical, Inc.
FDA (openFDA device enforcement)
Reported Jan 28, 2026
Brand Name: LEASEIR Product Name: LEASEIR MHR XCELL Model/Catalog Number: MHR 110-b Software Version: 1.5.0.0 Product…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Leaseir Technologies Slu
FDA (openFDA device enforcement)
Reported Jan 28, 2026
Mazor X robotic guidance system REF: TPL0059
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mazor Robotics Ltd.
FDA (openFDA device enforcement)
Reported Jan 28, 2026
MEDLINE beds labeled as: 1) Semi Electric Basic Homecare Bed, REF MDR107002E; 2) Semi Electric Basic Homecare Bed,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Medline Industries, LP
5 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 28, 2026
Merit Medical Inflation Device.basixCOMPAK.30 atm/bar.20 mL Reference Numbers: ENDO-AN2030/B IN4130/CNK IN4130/H…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Merit Medical Systems, Inc.
6 more products in this recall
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.