119 results
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45ms
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Sources: EU EUDAMED, US FDA
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Status: Open, Classified
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LINK SymphoKnee System L-Shaped Femoral Augment, Medial-Right/Lateral-Left, Sz 5-6 Tilastan, cemented. Intended for primary and revision total knee replacement. Item Number: 880-325/13
FDA Recall
Open, Classified
·Linkbio Corp.·Product code JWH·April 25, 2023
COAPTITE Injectable Implant, injectable, sterile, non-pyrogenic implant composed of spherical particles (75-125 microns in diameter of calcium hydroxylapatite (CaHA), suspended in aqueous based gel carrier. Gel carrier is composed of sodium carboxymethylcellulose, sterile water for injection, and glycerin. Product is packaged in a 1.0cc syringe and packed in a sterile pouch.
FDA Recall
Open, Classified
·Merz North America, Inc.·Product code LNM·September 30, 2020
Various products which were contract sterilized.
FDA Recall
Open, Classified
·Anewmed Corporation·Product code DQX·May 23, 2019
SofTech Pressure-Sensing Wheelchair Cushions
FDA Recall
Open, Classified
·Aquila Corporation·Product code KNN·July 6, 2023
APK2 Pressure-Sensing Wheelchair Cushions
FDA Recall
Open, Classified
·Aquila Corporation·Product code KNN·July 6, 2023
Baxter EXACTAMIX Inlet, Vented, Micro-Volume Inlet, REF H938175, for use in a pharmaceutical compounding device
FDA Recall
Open, Classified
·Baxter Healthcare Corporation·Product code LHI·August 20, 2024
Baxter EXACTAMIX Inlet, Vented, High Volume Inlet, REF H938174, for use in a pharmaceutical compounding device
FDA Recall
Open, Classified
·Baxter Healthcare Corporation·Product code LHI·August 20, 2024
Baxter EXACTAMIX Inlet, Non-Vented, High Volume Inlet, REF H938173, for use in a pharmaceutical compounding device
FDA Recall
Open, Classified
·Baxter Healthcare Corporation·Product code LHI·August 20, 2024
Baxter EXACTAMIX Inlet, Vented, Syringe Inlet, REF H938176, for use in a pharmaceutical compounding device
FDA Recall
Open, Classified
·Baxter Healthcare Corporation·Product code LHI·August 20, 2024
NO 4 TRIATHLON TS PLUS TIB INS X3 POLY 16 MM
FDA Recall
Open, Classified
·Howmedica Osteonics Corp.·Product code MBH·February 6, 2024
X3 TRIATHLON CS INSERT NO 3 10 MM
FDA Recall
Open, Classified
·Howmedica Osteonics Corp.·Product code MBH·February 6, 2024
NO 4 TRIATHLON TS PLUS TIB INS X3 POLY 16 MM
FDA Recall
Open, Classified
·Howmedica Osteonics Corp.·Product code MBH·February 6, 2024
X3 TRIATHLON CS INSERT NO 6 11 MM
FDA Recall
Open, Classified
·Howmedica Osteonics Corp.·Product code MBH·February 6, 2024
X3 TRIATHLON CS INSERT NO 7 9 MM
FDA Recall
Open, Classified
·Howmedica Osteonics Corp.·Product code MBH·February 6, 2024
NO 3 TRIATHLON TS PLUS TIB INS X3 POLY 11 MM
FDA Recall
Open, Classified
·Howmedica Osteonics Corp.·Product code MBH·February 6, 2024
X3 TRIATHLON CS INSERT NO 6 10 MM
FDA Recall
Open, Classified
·Howmedica Osteonics Corp.·Product code MBH·February 6, 2024
NO 4 TRIATHLON TS PLUS TIB INS X3 POLY 11 MM
FDA Recall
Open, Classified
·Howmedica Osteonics Corp.·Product code MBH·February 6, 2024
28MM -4 LFIT V40 HEAD, Catalog Number 6260-9-122
FDA Recall
Open, Classified
·Howmedica Osteonics Corp.·Product code JDG·October 15, 2021
LINK BiMobile Dual Mobility System E-Poly Liner for 28mm Head, 70mm Shell- Indicated for patients with mobility-limiting diseases, fractures or defects of the hip joint or proximal femur. Item Number: 184-280/12
FDA Recall
Open, Classified
·Waldemar Link GmbH & Co. KG (Mfg Site) Oststr. 4-10 Norderstedt Germany·Product code LZO·January 22, 2024
Tangent Endoscopy, Tangent Single Use Digital Catheter. Model Numbers: (1) TNG4002-IND. (2) TNG-4007-6pk.
FDA Recall
Open, Classified
·TANGENT ENDOSCOPY, LLC·Product code FBN·March 23, 2026