36 results
·
71ms
·
Sources: EU EUDAMED, US FDA
UNKNOWN HIP FEMORAL HEAD
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS INC US·Product code LPH·January 21, 2026
UNK HIP FEMORAL STEM SUMMIT
FDA Adverse Event
Malfunction
·DEPUY ORTHOPAEDICS INC US·Product code LPH·January 21, 2026
ZIMMER Oscillating Saw Blade -Cutting 75mm x 19mm x 1.00/1.27mm.intended for bone or cartilage in orthopedic procedures. Manufactured By: Synvasive Technology, Inc., a Subsidiary of Zimmer
FDA Recall
Terminated
·Synvasive Technology Inc·Product code GFA·July 27, 2018
BONE SCREW SELF-TAPPING 6.5 MM DIA. 20 MM LENGTH
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code LPH·August 15, 2025
BONE SCREW SELF-TAPPING 6.5 MM DIA. 25 MM LENGTH
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code LPH·August 15, 2025
BONE SCREW SELF-TAPPING 35 MM LENGTH 6.5 MM DIA.
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code LPH·August 15, 2025
BONE SCREW SELF-TAPPING 6.5 MM DIA. 20 MM LENGTH
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code LPH·August 15, 2025
SHELL POROUS WITH MULTI HOLES 58 MM
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code LPH·August 15, 2025
XLPE 10 DEG POLY LINER 58X36
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JWH·August 15, 2025
PENCAN®
FDA Adverse Event
Injury
·B. BRAUN MELSUNGEN AG·Product code BSP·June 24, 2019
VICRYL POLYGLACTIN 910 SUTURE UNKNOWN PRODUCT
FDA Adverse Event
Injury
·ETHICON INC.·Product code GAM·April 4, 2025
VICRYL POLYGLACTIN 910 SUTURE UNKNOWN PRODUCT
FDA Adverse Event
Injury
·ETHICON INC.·Product code GAM·April 4, 2025
VICRYL POLYGLACTIN 910 SUTURE UNKNOWN PRODUCT
FDA Adverse Event
Injury
·ETHICON INC.·Product code GAM·April 4, 2025
VICRYL POLYGLACTIN 910 SUTURE UNKNOWN PRODUCT
FDA Adverse Event
Injury
·ETHICON INC.·Product code GAM·April 4, 2025
VICRYL POLYGLACTIN 910 SUTURE UNKNOWN PRODUCT
FDA Adverse Event
Injury
·ETHICON INC.·Product code GAM·April 4, 2025
Margron DTC Hip Replacement System; Margron hip - Femoral stem 3+0, sterile, Portland Orthopaedics Inc., St. Clair, MI; REF 1-649-000. Product is used for Orthopedic surgery.
FDA Recall
Terminated
·Portland Orthopaedics Pty, Ltd.
1 South Street, Suite 3, Level 5
Saint George Hospital
Kogarah Australia·Product code MEH·January 11, 2008
ETHLN BLK 18IN 4-0 S/A P-3 PRM MP
FDA Adverse Event
Malfunction
·ETHICON INC.·Product code GAR·December 7, 2022
VALIANT
FDA Adverse Event
Injury
·MEDTRONIC IRELAND·Product code MIH·September 12, 2014
SHOULDER PACK CODE 900-2766 CONTENTS: (1) STAPLE SKIN 35 WIDE LIF (1) *GOBAN SELF-ADH 4" X 5YD WRAP TAN LATEX (2) U-DRAPE 60" X 70" WITAPE SPLIT 6" X 21" (1) TABLE COVER 44" X 90" (4) TOWELS ABSORBENT 15" X 20" LIF (2) TUBE SUCTION CONNECT" X 12' LIF (1) SKIN MARKER INK W/8 LABEL/TIME OUT/RULER LIF (1) BAG SUTURE FLORAL (1) SYRINGE 20cc W/0 NEEDLE LUER/LOCK LIF (1) SCALPEL WEIGHTED SAFETY #11 (1) NEEDLE SPINAL ANESTH 18G X 3% LIF (1) DRAPE INCISE ANTIMICROBIAL 23" X 17" LIF (1) CHLORAPREP 26ML APLICATOR TEAL LIF (2) ATTACHABLE POUCH BEACH CHAIR 35" X 43" WITH SUCTION PART (4) DRAPE UTILITY WITAPE L/F (4) STERI-DRAPE SMALL TOWEL DRAPE NPN-STERILE 17" X 11" LIF (1) BOWL UTILITY 32oz. (1) STOCKINETTE 6" X 48" L/F (5) LAP SPONGE PREWASH 18" X 18" XRD LIF (1) WRAPPER 24" X 24" (1) NEEDLE HYPODERMIC 22G X 1 % (1) GOWN SURG REINFORCED X-LARGE TOWEL I WRAP (1) GOWN MICROCOOL IMPERV. EXTRA LONG X-LARGE (2) DRAPE ORTHOPEDIC SPLIT (1) MAYO STAND COVER REINFORCED LIF Product Usage: EO sterilized surgical convenient packs packaged into polyester/polyethylene breather bag with Tyvek double vents.
FDA Recall
Terminated
·Customed, Inc Calle Igualdad Final # 7·Product code OJH·May 20, 2014
Margron DTC Hip Replacement System; Margron hip - Femoral stem 5+0, sterile, Portland Orthopaedics Inc., St. Clair, MI; REF 1-651-000. Product is used for Orthopedic surgery.
FDA Recall
Terminated
·Portland Orthopaedics Pty, Ltd.
1 South Street, Suite 3, Level 5
Saint George Hospital
Kogarah Australia·Product code MEH·January 11, 2008