10,000 results
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46ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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TRIATHLON PS X3 TIBIAL INSERT
FDA Adverse Event
Malfunction
·STRYKER ORTHOPAEDICS-MAHWAH·Product code MBH·May 10, 2023
TRIATHLON CR X3 TIBIAL INSERT
FDA Adverse Event
Malfunction
·STRYKER ORTHOPAEDICS-MAHWAH·Product code MBH·March 6, 2023
SAW BLADE STRYKER UNIV WIDE TOTAL ANKLE .500 IN
FDA Adverse Event
Malfunction
·WRIGHT MEDICAL TECHNOLOGY INC·Product code GFA·July 28, 2025
GMRS EXTENSION PC 40MM LF
FDA Adverse Event
Injury
·STRYKER ORTHOPAEDICS-MAHWAH·Product code KRO·February 26, 2024
INBONE ML PLATE
FDA Adverse Event
Malfunction
·WRIGHT MEDICAL TECHNOLOGY INC·Product code LXH·December 18, 2025
X3 TRIATHLON CS INSERT NO 4 9MM
FDA Adverse Event
Malfunction
·STRYKER ORTHOPAEDICS-MAHWAH·Product code MBH·September 12, 2024
PRIMARY TRIT HEMI CLUSTER HOLE CUP 56MM
FDA Adverse Event
Malfunction
·STRYKER ORTHOPAEDICS-MAHWAH·Product code LPH·August 22, 2025
TRIATHLON PS X3 TIBIAL INSERT
FDA Adverse Event
Malfunction
·STRYKER ORTHOPAEDICS-MAHWAH·Product code MBH·April 22, 2024
TRIATHLON PS X3 TIBIAL INSERT
FDA Adverse Event
Malfunction
·STRYKER ORTHOPAEDICS-MAHWAH·Product code MBH·November 8, 2023
X3 TRIATHLON CS INSERT NO 7 16MM
FDA Adverse Event
Malfunction
·STRYKER ORTHOPAEDICS-MAHWAH·Product code MBH·October 8, 2024
TRIDENT 10 X3 INSERT 32MM ID
FDA Adverse Event
Malfunction
·STRYKER ORTHOPAEDICS-MAHWAH·Product code LPH·February 16, 2021
INBONE TIB TRAY RT SZ 3 LNG
FDA Adverse Event
Injury
·WRIGHT MEDICAL TECHNOLOGY INC·Product code HSN·April 9, 2024
TRIATHLON CR X3 TIBIAL INSERT
FDA Adverse Event
Malfunction
·STRYKER ORTHOPAEDICS-MAHWAH·Product code MBH·April 10, 2024
INBONE STEM TIBIAL BASE 16MM RIGHT AND LEFT
FDA Adverse Event
Injury
·WRIGHT MEDICAL TECHNOLOGY INC·Product code HSN·April 9, 2024
INBONE TALAR STEM 10MM LG
FDA Adverse Event
Malfunction
·WRIGHT MEDICAL TECHNOLOGY INC·Product code HSN·May 15, 2025
Plastic bottle containing 10.5 mL of IgG Conjugate Product Usage: Product is a used as a counterstain for various indirect fluorescent assay kits
FDA Recall
Terminated
·Bion Enterprises Ltd·Product code GQO·January 23, 2013
Antisera, Cf, Herpesvirus Hominis 1,2
FDA classification
FDA Class 2
·Antisera, Cf, Herpesvirus Hominis 1,2
GEO S.R.L.
FDA registration
GEO S.R.L.·1 product·🇮🇹 Italy
GBO MEDIZINTECHNIK AG
FDA registration
GBO MEDIZINTECHNIK AG·4 products·🇩🇪 Germany
He Gao Plastic Factory
FDA registration
He Gao Plastic Factory·2 products·🇨🇳 China