212 results · 14ms · Sources: EU EUDAMED, US FDA

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Dental pins - TMS LINK PLUS Self-Threading Pins - Product Usage: implanted into the teeth or for lab use for dental restoration purposes. The normal procedure requires a hole to be drilled into the tissue of a tooth with an intraoral drill prior to installation. Model number/Catalog number: L741

FDA Recall
Open, Classified ·Coltene Whaledent Inc·Product code EBL·March 18, 2021

Biomet SpinalPak Non-invasive Spine Fusion Stimulator System- Indicated for the treatment of an established nonunion acquired secondary to trauma, excluding vertebrae and all flat bones, Part Number: 1067716

FDA Recall
Open, Classified ·EBI, LLC·Product code LOF·March 22, 2024

48" Lead Wires, Replacement Part Number: 1067724-4

FDA Recall
Open, Classified ·EBI, LLC·Product code LOF·March 22, 2024

20" Lead Wires, Replacement Part Number: 1067724-2

FDA Recall
Open, Classified ·EBI, LLC·Product code LOF·March 22, 2024

Biomet OrthoPak Non-invasive Bone Growth Stimulator System-Indicated for the treatment of an established nonunion acquired secondary to trauma, excluding vertebrae and all flat bones. Part Number: 1067718

FDA Recall
Open, Classified ·EBI, LLC·Product code LOF·March 22, 2024

Bio-Rad, REF: 12005660, QXDx BCR-ABL %IS Kit

FDA Recall
Open, Classified ·Bio-Rad Laboratories·Product code OYX·February 15, 2024

Brand Name: Xpert BCR-ABL Ultra Model/Catalog Number: GXBCRABL-10

FDA Recall
Open, Classified ·Cepheid·Product code OYX·October 30, 2025

Brand Name: Xpert BCR-ABL Ultra Model/Catalog Number: GXBCRABL-US-10

FDA Recall
Open, Classified ·Cepheid·Product code OYX·October 30, 2025

Omnipod 5 Automated Insulin Delivery System

FDA Recall
Open, Classified ·Product code QFG·February 28, 2023

NuVasive MD Pulse III Multimodality System REF 1881500 Pulse Software version 369-BL.US and 369-BLN.US

FDA Recall
Open, Classified ·NuVasive Inc·Product code OLO·July 19, 2022

HydroSurg Plus Laparoscopic Irrigator with Nezhat-Dorsey SmokEvac Trumpet Valve, Handle only, with Cojoined Suction and Irrigation Tubing, Catalog number 0026880

FDA Recall
Open, Classified ·Davol, Inc.·Product code GCJ·June 7, 2022

HydroSurg Plus Laparoscopic Irrigator with Nezhat-Dorsey SmokEvac Trumpet Valve, 33cm Tip and Cojoined Suction and Irrigation Tubing, Catalog Number 0026870

FDA Recall
Open, Classified ·Davol, Inc.·Product code GCJ·June 7, 2022

Stryker Sustainability Solution Color Cuff 24" (Yellow) Quick Connect Dual Port Single Bladder REF 5921-024-235 Stryker Sustainability Solution Color Cuff 18" (Red), Quick Connect Dual Port Single Bladder REF 5921-018-135 Stryker Sustainability Solution Color Cuff 18" (Red) Dual Port Single Bladder REF 5921-018-235.

FDA Recall
Open, Classified ·Stryker Sustainability Solutions·Product code KCY·March 12, 2026

TriMed Countersink 1.7mm, HCS, REF HSINK-1.7, nonsterile, Rx. The firm name on the label is TriMed Inc., Santa Clarita, CA.

FDA Recall
Open, Classified ·TriMed Inc.·Product code LXH·September 28, 2018

TriMed Locking Drill Guide, 2.3mm, REF GUIDELCBS-2.3, nonsterile, Rx. The firm name on the label is TriMed Inc., Santa Clarita, CA.

FDA Recall
Open, Classified ·TriMed Inc.·Product code LXH·September 28, 2018

TriMed Hex Driver 1.2, 55mm AO Cannulated, REF HXDRIVR-1.2C AO, nonsterile, Rx. The firm name on the label is TriMed Inc., Santa Clarita, CA.

FDA Recall
Open, Classified ·TriMed Inc.·Product code LXH·September 28, 2018

Baxter Spectrum IQ Infusion System with Dose IQ Safety Software, Product Code 3570009

FDA Recall
Open, Classified ·Baxter Healthcare Corporation·Product code FRN·October 2, 2024

TriMed Peg Guide Extender, REF PEG-XTNDR, nonsterile, Rx. The firm name on the label is TriMed Inc., Santa Clarita, CA.

FDA Recall
Open, Classified ·TriMed Inc.·Product code LXH·September 28, 2018

TriMed Wrist Hook Dorsal Impactor, REF IMPCT-WHD; and TriMed Wrist Hook Volar Impactor, REF IMPCT-WHV, both nonsterile, Rx, The firm name on the labels is TriMed Inc., Santa Clarita, CA.

FDA Recall
Open, Classified ·TriMed Inc.·Product code LXH·September 28, 2018

Medtronic Reveal LINQ LNQ11 / PA96000

FDA Recall
Open, Classified ·Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)·Product code MXD·June 1, 2021