1,290 results · 77ms · Sources: EU EUDAMED, US FDA

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NEURO-SP-1/2X1/2"-STRL 20/CS

FDA Adverse Event
Malfunction ·MEDSORB DOMINICANA, S.A.·Product code EFQ·April 8, 2025

DEROYAL INDUSTRIES, INC.

FDA Adverse Event
UNIMED SURGICAL·Product code GEI·June 6, 2012

DEROYAL INDUSTRIES, INC.

FDA Adverse Event
Other ·UNIMED SURGICAL PRODUCTS, INC.·Product code GEI·December 22, 2011

NEURO-SP-1/2X1/2"-STRL 20/CS

FDA Adverse Event
Malfunction ·MEDSORB DOMINICANA, S.A.·Product code EFQ·January 20, 2025

TEMPLE TOUCH PRO SENSOR UNIT, NON-INVASIVE CORE TEMP MONT

FDA Adverse Event
Malfunction ·MEDISIM LTD.·Product code FLL·April 14, 2025

SAFETYSCALPEL ASMBD #3 FITMENT, #11 BLADE, BLUE NS

FDA Adverse Event
Malfunction ·S&S SURGICAL PRODUCTS INC·Product code GDZ·May 8, 2025

NEURO-SP-1/2X1/2"-STRL 20/CS

FDA Adverse Event
Malfunction ·MEDSORB DOMINICANA, S.A.·Product code EFQ·January 20, 2025

NEONTAL TEMPERATURE SKIN SENSO, NOVAPLUS

FDA Adverse Event
Malfunction ·DEROYAL CIENTIFICA DE LATINOAMERICA S.R.L·Product code FMT·December 16, 2025

DEROYAL

FDA Adverse Event
Malfunction ·DEROYAL INDUSTRIES, INC.·Product code GES·April 26, 2018

CIRCUMCISION CLAMP SIZE 1.3 CM

FDA Adverse Event
Malfunction ·DEROYAL INDUSTRIES, INC.·Product code HFX·March 9, 2011

CIRCUMCISION CLAMP SIZE 1.3 CM

FDA Adverse Event
Other ·DEROYAL INDUSTRIES, INC.·Product code HFX·March 9, 2011

ARM BOARD, IV, FLEXIBLE, 4" X 9", BLUE PURR, OUILOCK 

FDA Adverse Event
Malfunction ·ORTHO & SURGICAL PRODUCTS ENTERPRISES S.A.·Product code KMK·April 27, 2026

SKIN STAPLER 35W

FDA Adverse Event
Injury ·TELEFLEX LLC·Product code QQS·December 23, 2025

3 PORT MANIFOLD KIT

FDA Adverse Event
Malfunction ·DEROYAL INTERCONTINENTAL, S.R.L·Product code OEQ·July 28, 2025

SAFETYSCALPEL ASMBD #3 FITMENT, #11 BLADE, BLUE NS

FDA Adverse Event
Malfunction ·S&S SURGICAL PRODUCTS INC·Product code GDZ·July 16, 2025

SAFETYSCALPEL ASMBD #3 FITMENT, #10 BLADE, BLACK NS

FDA Adverse Event
Malfunction ·S&S SURGICAL PRODUCTS INC·Product code GDZ·July 16, 2025

NEURO SPGS-3/4X6"-20/C

FDA Adverse Event
Malfunction ·MEDSORB DOMINICANA, S.A.·Product code EFQ·July 16, 2025

FOLEY CATHETER, 400 SERIES 10 FR

FDA Adverse Event
Malfunction ·DEROYAL INDUSTRIES, INC.·Product code EYC·July 7, 2025

ARM BOARD, IV, FLEXIBLE, 4" X 9", BLUE PURR, OUILOCK 

FDA Adverse Event
Malfunction ·ORTHO & SURGICAL PRODUCTS ENTERPRISES S.A.·Product code KMK·April 27, 2026

ARM BOARD, IV, FLEXIBLE, 4" X 9", BLUE PURR, OUILOCK 

FDA Adverse Event
Malfunction ·ORTHO & SURGICAL PRODUCTS ENTERPRISES S.A.·Product code KMK·April 27, 2026