35 results
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17ms
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Sources: EU EUDAMED, US FDA
Filters
FDA Recall
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Titanium MPJ (Toe Implant)TOE JOINT TITANIUM NPC LG, Part ID 16816
FDA Recall
Terminated
·BioPro, Inc.·Product code KWD·February 1, 2022
Titanium MPJ (Toe Implant)TOE JOINT TITANIUM PC SM, Part ID 17035
FDA Recall
Terminated
·BioPro, Inc.·Product code KWD·February 1, 2022
Titanium MPJ (Toe Implant) TOE JOINT TITANIUM PC M/L, Part ID 17037
FDA Recall
Terminated
·BioPro, Inc.·Product code KWD·February 1, 2022
Titanium MPJ (Toe Implant) TOE JOINT TITANIUM NPC MS, Part ID 17198
FDA Recall
Terminated
·BioPro, Inc.·Product code KWD·February 1, 2022
Titanium MPJ (Toe Implant) TOE JOINT TITANIUM NPC MD, Part ID 16814
FDA Recall
Terminated
·BioPro, Inc.·Product code KWD·February 1, 2022
Titanium MPJ (Toe Implant) TOE JOINT TITANIUM NPC SM, Part ID 16813
FDA Recall
Terminated
·BioPro, Inc.·Product code KWD·February 1, 2022
Titanium MPJ (Toe Implant) TOE JOINT TITANIUM PC MS, Part ID 17197
FDA Recall
Terminated
·BioPro, Inc.·Product code KWD·February 1, 2022
Titanium MPJ (Toe Implant) TOE JOINT TITANIUM PC MD, Part ID 17036
FDA Recall
Terminated
·BioPro, Inc.·Product code KWD·February 1, 2022
Titanium MPJ (Toe Implant) TOE JOINT TITANIUM PC LG, Part ID 17038
FDA Recall
Terminated
·BioPro, Inc.·Product code KWD·February 1, 2022
Titanium MPJ (Toe Implant) TOE JOINT TITANIUM NPC ML, Part ID 16815
FDA Recall
Terminated
·BioPro, Inc.·Product code KWD·February 1, 2022
Stryker Biotech OP-1 Putty (OP-1, BMP-7, bone morphogenetic protein) "Catalog numbers: 300-50, 300-55 OP-1 Putty is authorized by Federal law for use as an alternative to autograft in compromised patients requiring revision posterolateral (intertransverse) lumbar spinal fusion, for whom autologous bone and bone marrow harvest are not feasible or are not expected to promote fusion. Examples of compromising factors include osteoporosis, smoking and diabetes.
FDA Recall
Terminated
·Stryker Biotech·Product code OJZ·October 25, 2010
Left Locking 2st MTP/MPJ Combo Fusion Plate. Product labeled in part, "ACUMED 5885 NW Cornelius pass Road Hillsboro, OR. 97124-9432... Size: Left Locking 2st MTP/MPJ Combo Fusion Plate... REF 70-0036-S... LOT W58123".
FDA Recall
Terminated
·Acumed LLC·Product code HWC·February 14, 2008
Right Locking 1st MTP/MPJ Combo Fusion Plate. Product labeled in part, "ACUMED 5885 NW Cornelius pass Road Hillsboro, OR. 97124-9432... Size: Right Locking 1st MTP/MPJ Combo Fusion Plate... REF 70-0037-S... LOT W58148".
FDA Recall
Terminated
·Acumed LLC·Product code HWC·February 14, 2008
TrueDent Magenta, TDM130, Model No. OBJ-09166 Light-curable methacrylate-based resin that enables fabrication of dental appliances
FDA Recall
Completed
·STRATASYS LTD·Product code EBI·January 19, 2024
TrueDent White, TDM110, Model No. OBJ-09168 Light-curable methacrylate-based resin that enables fabrication of dental appliances
FDA Recall
Completed
·STRATASYS LTD·Product code EBI·January 19, 2024
TrueDent Yellow, TDM140, Model No. OBJ-09169 Light-curable methacrylate-based resin that enables fabrication of dental appliances
FDA Recall
Completed
·STRATASYS LTD·Product code EBI·January 19, 2024
TrueDent Cyan, TDM 120, Model No. OBJ-09165 Light-curable methacrylate-based resin that enables fabrication of dental appliances
FDA Recall
Completed
·STRATASYS LTD·Product code EBI·January 19, 2024
TrueDent Clear, TDM 100, Model No. OBJ-09164 Light-curable methacrylate-based resin that enables fabrication of dental appliances
FDA Recall
Completed
·STRATASYS LTD·Product code EBI·January 19, 2024
J-VAC Reservoir is a component of the J-VAC Closed Wound Drainage System. This system is a sterile, portable system used for closed wound drainage. This system is composed of two parts: the J-VAC Reservoir and Suction Drains.
FDA Recall
Terminated
·Ethicon, Inc US·Product code GCY·August 31, 2005
Invacare Power Wheelchair, one per box To provide mobility to a person restricted to a sitting position.
FDA Recall
Terminated
·Invacare Corporation·Product code ITI·June 4, 2013