34 results · 26ms · Sources: EU EUDAMED, US FDA

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SS 4.5MM DIAMOND TIP TROCAR WITH LARGE GLOVES Catalog Number:B1559

FDA Recall
Terminated ·Busse Hospital Disposables, Inc.·Product code FBR·February 22, 2022

Instructions for Use for all model numbers of the Medtronic Abre Venous Self-Expanding Stent System.

FDA Recall
Terminated ·Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)·Product code QAN·November 19, 2021

MADSEN ACCUSCREEN TEOAE/DPOAE/ABR Probe (P/N 8-69-41100)

FDA Recall
Open, Classified ·PATH Landsberger Str. 65 Germering Germany·Product code GWJ·November 6, 2025

POLYSIN (Polyglycolic Acid) suture, HSM9 5-0 BR PGA Part Number G503N

FDA Recall
Open, Classified ·SURGICAL SPECIALTIES·Product code GAM·March 26, 2024

Abre Venous Self-expanding Stent System, Product Numbers: a) AB9U14080090; b) AB9U18100090; c) AB9G14100090

FDA Recall
Open, Classified ·Medtronic Inc.·Product code QAN·February 16, 2024

Medonic M-Series Hematology Analyzer M16S BD ABR US Product code: 1400075; OUS Product code 1400011

FDA Recall
Terminated ·Clinical Diagnostic Solutions, Inc.·Product code GKZ·January 2, 2020

Abre Venous Self-Expanding Stent System, Model numbers AB9G14120090 AB9G12100090 AB9G14080090 AB9G12080090 AB9U12060090 AB9U14100090 AB9U14080090 AB9U12080090 AB9U14060090 AB9G14100090 AB9G12060090

FDA Recall
Open, Classified ·Medtronic Inc·Product code QAN·December 4, 2025

Medtronic Abre Venous Self-expanding Sent System, Catalog number REF AB9U16080090 - Product Usage: intended for use in the iliofemoral veins for the treatment of symptomatic venous outflow obstruction.

FDA Recall
Terminated ·Medtronic Inc.·Product code QAN·March 16, 2021

Smith & Nephew Endoscopic Disposable Blades: NOTCHBLASTER ABR,EP-1,5.5 DSPL Part #: 7205329. DYONICS Series 3000 BONECUTTER Disposable Arthroscopic Surgery Blades are indicated for resection of soft and osseous tissues in large and small articular cavities. Specific applications may include knee and shoulder reconstructive procedures such as notchplasty and acromioplasty.

FDA Recall
Terminated ·Smith & Nephew, Inc. Endoscopy Division·Product code NBH·May 7, 2009

Euflexxa (1% sodium hyaluronate). Pre-filled syringe, Rx only, 3 syringes per carton; Manufactured by Ferring Pharmaceuticals In, Parsippany, NJ 07054; Manufactured by Bio-Technology General (Israel Ltd. Be er Tuvia, Kiryat Malachi 83104 Israel. Indicated for the treatment of pain in osteoarthritis of the knee in patients who have failed to respond adequately to conservative non-pharmacologic therapy and simple analgesics.

FDA Recall
Terminated ·Ferring Pharmaceuticals Inc·Product code MOZ·April 16, 2010

LHB, Type I First Aid Kit Perishable, Non-Aspirin 4/pg, Aspirin 4/pg and Povidone Iodine, antiseptic towelette. Kit Number: 2113110. First Aid Kit.

FDA Recall
Terminated ·Lighthouse For The Blind·Product code LRR·March 22, 2013

LHB, Antiseptic Kit, Povidone Swab, Gauze Pads, and non-stick pads. Kit Number: 2113305. First Aid Kit.

FDA Recall
Terminated ·Lighthouse For The Blind·Product code LRR·March 22, 2013

LHB, First Aid Type I Individual Kit, NSN: 6545-00-656-1092, antiseptics, Kit number: 2114002. First Aid Kit.

FDA Recall
Terminated ·Lighthouse For The Blind·Product code LRR·March 22, 2013

LHB, Perishable Items Pack Type I , Kit Number: 2114002-100. First Aid Kit.

FDA Recall
Terminated ·Lighthouse For The Blind·Product code LRR·March 22, 2013

BostonSight SCLERAL Lens

FDA Recall
Open, Classified ·Boston Foundation For Sight·Product code HQD·June 10, 2025

LHB, First Aid Type IV Belt Type, NSN #6545-01-010-7754. Kit number: 114016. First Aid Kit.

FDA Recall
Terminated ·Lighthouse For The Blind·Product code LRR·March 22, 2013

LHB, Perishable Items Pack Type IV. Kit number: 2114016-100. First Aid Kit.

FDA Recall
Terminated ·Lighthouse For The Blind·Product code LRR·March 22, 2013

LHB, Perishable Item Pack Type III. Kit number: 2114011-100. First Aid Kit.

FDA Recall
Terminated ·Lighthouse For The Blind·Product code LRR·March 22, 2013

LHB, First Aid Type III, NSN # 6545-00-656-1094, Kit number: 2114011. First Aid Kit.

FDA Recall
Terminated ·Lighthouse For The Blind·Product code LRR·March 22, 2013

BostonSight PROSE Lens.

FDA Recall
Open, Classified ·Boston Foundation For Sight·Product code HQD·June 10, 2025