14 results
·
19ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Recall
×
Advantx 1 LC2 Model 2105657 Angiographic X-ray System
FDA Recall
Terminated
·General Electric Med Systems·Product code IZI·March 24, 2004
Advantx 1 LC2 Model 45562281 Angiographic X-ray System
FDA Recall
Terminated
·General Electric Med Systems·Product code IZI·March 24, 2004
Advantx 1 LC1 Model 45258230 Angiographic X-ray System
FDA Recall
Terminated
·General Electric Med Systems·Product code IZI·March 24, 2004
Advantx 1 LC1 Model 46-279781P1 Angiographic X-ray System
FDA Recall
Terminated
·General Electric Med Systems·Product code IZI·March 24, 2004
MAC" Two-Lumen Central Venous Access Kit for use with 7.5 - 8 Fr. Catheters REF ASK-11142-LC2 UDI code: (01)10801902206807(17)270531(11)251211(10)33F25M0670 The MAC Multi-Lumen Central Venous Access Device permits short-term (<30 days) venous access and catheter introduction to the central circulation.
FDA Recall
Open, Classified
·ARROW INTERNATIONAL, LLC·Product code OFC·March 11, 2026
(1) Percutaneous Sheath Introducer Kit with Integral Hemostasis Valve/Side Port, Sharps Safety Features, and Maximal Barrier Precautions for use with 7.5 - 8 Fr. Catheters, Part Number: ASK-09803-WBH1; (2) Percutaneous Sheath Introducer Kit with Integral Hemostasis Valve/Side Port, Sharps Safety Features, and Maximal Barrier Precautions for use with 7.5 - 8 Fr. Catheters, Part Number: ASK-09903-KH; (3) Percutaneous Sheath Introducer Kit for use with 7.5 - 8 Fr. Catheters, Part Number: ASK-09903-LC; (4) PSI Kit for use with 7.5 - 8 Fr. Catheters, Part Number: ASK-09903-PHP; (5) Percutaneous Sheath Introducer Kit for use with 7.5 - 8 Fr. Catheters, Part Number: ASK-09907-LGH1; (6) Arrow PSI Kit, Part Number: CDC-09803-1A; (7) Arrow PSI Kit, Part Number: CDC-09903-1A
FDA Recall
Terminated
·Arrow International Inc·Product code DYB·December 22, 2017
ETI-MP IgM Enzyme-Linked Immunosorbent Assay (ELISA) for the qualitative detection of specific IgM antibodies to Mycoplasma pneumoniae in human serum. Test kit for 192 determinations. Catalog No. 4700. For In Vitro Diagnostic use. manufactured for DiaSorin Inc., 1950 Northwestern Avenue P.O. Box 285, Stillwater, MN 55082-0285
FDA Recall
Terminated
·Diasorin Inc.·Product code LAZ·October 20, 2004
Frontier Devices, REF: 301.914S2, 14 mm Distraction Pin, 10 double packs , Rx Only, Sterile
FDA Recall
Open, Classified
·Folsom Metal Products, Inc.·Product code GCZ·August 21, 2025
Centurion-Trays EBSI1021 VALVE CHANGE KIT- DOUBLE
FDA Recall
Terminated
·Centurion Medical Products Corporation·Product code KCZ·December 11, 2019
Frontier Devices, REF: 301.914S1, 14 mm Distraction Pin, 10 single packs , Rx Only, Sterile
FDA Recall
Open, Classified
·Folsom Metal Products, Inc.·Product code GCZ·August 21, 2025
Frontier Devices, REF: 301.914S1, 14 mm Distraction Pin, 5 single packs , Rx Only, Sterile
FDA Recall
Open, Classified
·Folsom Metal Products, Inc.·Product code GCZ·August 21, 2025
Frontier Devices, REF: 301.916S1, 16 mm Distraction Pin, 10 single packs , Rx Only, Sterile
FDA Recall
Open, Classified
·Folsom Metal Products, Inc.·Product code GCZ·August 21, 2025
Frontier Devices, REF: 301.912S1, 12 mm Distraction Pin, 10 single packs , Rx Only, Sterile
FDA Recall
Open, Classified
·Folsom Metal Products, Inc.·Product code GCZ·August 21, 2025
Frontier Devices, REF: 301.912S2, 12 mm Distraction Pin, 10 double packs , Rx Only, Sterile
FDA Recall
Open, Classified
·Folsom Metal Products, Inc.·Product code GCZ·August 21, 2025