31 results
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13ms
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Sources: EU EUDAMED, US FDA
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Status: Open, Classified
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EMPOWR Locking Femoral Impactor , Part # 800-05-035, packaged in instrument tray FA EMP PAT TOOL KIT Part # 800-99-096
FDA Recall
Open, Classified
·Product code LXH·February 4, 2019
A.L.P.S. mvX- ANATOMIC LAT FIB PLATE 6H RT: Anatomic Lateral Fibula Plate, 6-hole, Right Model/Catalog Number: 770708062
FDA Recall
Open, Classified
·Tyber Medical·Product code HRS·January 21, 2025
A.L.P.S. mvX -ANATOMIC LAT FIB PLATE 4H RT: Anatomic Lateral Fibula Plate, 4-hole, Right Model/Catalog Number: 770708042
FDA Recall
Open, Classified
·Tyber Medical·Product code HRS·January 21, 2025
The Sofia 2 Flu + SARS Antigen FIA employs immunofluorescence technology in a sandwich design that is used with Sofia 2 to detect nucleocapsid protein from influenza A, influenza B, and SARS-CoV-2. This test allows for the detection of SARS-CoV and SARS-CoV-2, but does not differentiate between the two viruses.
FDA Recall
Open, Classified
·Quidel Corporation·Product code QMN·January 3, 2024
A.L.P.S. mvX -ANATOMIC LAT FIB PLATE 6H LT- Anatomic Lateral Fibula Plate, 6-hole, Left Intended for Fixation of fractures of the distal tibia Model/Catalog Number: 770708061
FDA Recall
Open, Classified
·Tyber Medical·Product code HRS·January 21, 2025
A.L.P.S. mvX - ANATOMIC LAT FIB PLATE 4H LT: Anatomic Lateral Fibula Plate, 4-hole, Left Intended for Fixation of fractures of the distal tibia Model/Catalog Number: 770708041
FDA Recall
Open, Classified
·Tyber Medical·Product code HRS·January 21, 2025
A.L.P.S. mvX- ANATOMIC LAT FIB PLATE 10H RT- Anatomic Lateral Fibula Plate, 10-Hole, Right. Intended forFixation of fractures of the distal tibia Model/Catalog Number: 770708102 Product Description:
FDA Recall
Open, Classified
·Tyber Medical·Product code HRS·January 21, 2025
A.L.P.S. mvX-P: ANATOMIC LAT FIB PLATE 12H LT- Anatomic Lateral Fibula Plate, 12-Hole, Left. Inended for Fixation of fractures of the distal tibia Model/Catalog Number: 770708121
FDA Recall
Open, Classified
·Tyber Medical·Product code HRS·January 21, 2025
A.L.P.S. mvX- Product Name: ANATOMIC LAT FIB PLATE 10H LT Anatomic Lateral Fibula Plate, 10-Hole, Left. Intended Fixation of fractures of the distal tibia Model/Catalog Number: 770708101
FDA Recall
Open, Classified
·Tyber Medical·Product code HRS·January 21, 2025
A.L.P.S. mvX- ANATOMIC LAT FIB PLATE 8H LT: Anatomic Lateral Fibula Plate, 8-hole, Left Intended to bridge or otherwise stabilize bone fragments to facilitate healing. Model/Catalog Number: 770708081
FDA Recall
Open, Classified
·Tyber Medical·Product code HRS·January 21, 2025
A.L.P.S. mvX- ANATOMIC LAT FIB PLATE 12H RT- Anatomic Lateral Fibula Plate, 12-Hole, Right. Intended for Fixation of fractures of the distal tibia Model/Catalog Number: 770708122 Product Description:
FDA Recall
Open, Classified
·Tyber Medical·Product code HRS·January 21, 2025
A.L.P.S. mvX- ANATOMIC LAT FIB PLATE 8H RT: Anatomic Lateral Fibula Plate, 8-hole, Right Indicated for use in Fixation of fractures of the distal tibia Model/Catalog Number: 77070802
FDA Recall
Open, Classified
·Tyber Medical·Product code HRS·January 21, 2025
Posi-Stop Injection Needle, 23 Gauge, Catalog Number: 4706
FDA Recall
Open, Classified
·Hobbs Medical, Inc.·Product code FBK·October 4, 2024
Posi-Stop Injection Needle, 25 Gauge, Catalog Number: 4723
FDA Recall
Open, Classified
·Hobbs Medical, Inc.·Product code FBK·October 4, 2024
Posi-Stop Injection Needle, 23 Gauge, Catalog Number: 4721
FDA Recall
Open, Classified
·Hobbs Medical, Inc.·Product code FBK·October 4, 2024
Hobbs Posi-Stop Injection Needle Catalog Number: 4718
FDA Recall
Open, Classified
·Hobbs Medical, Inc.·Product code FBK·July 29, 2022
Hobbs Posi-Stop Injection Needle Catalog Number: 4722
FDA Recall
Open, Classified
·Hobbs Medical, Inc.·Product code FBK·July 29, 2022
Posi-Stop Injection Needle, 25 Gauge, Catalog Number: 4722
FDA Recall
Open, Classified
·Hobbs Medical, Inc.·Product code FBK·October 4, 2024
Hobbs Posi-Stop Injection Needle Catalog Number: 4720
FDA Recall
Open, Classified
·Hobbs Medical, Inc.·Product code FBK·July 29, 2022
ORISE Gel Syringe Submucosal Lifting Agent Kits: indicated for use in gastrointestinal endoscopic procedures for submucosal lift of polyps, adenomas, early-stage cancers or other gastrointestinal mucosal lesions, prior to excision with a snare or other suitable endoscopic device UPN: (1)Twin Pack Box 1 M00519210; (2)Twin Pack Box 10 M00519211; (3)Single Pack Box 10 M00519231
FDA Recall
Open, Classified
·Boston Scientific Corporation·Product code FBK·October 10, 2022