28 results
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13ms
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Sources: EU EUDAMED, US FDA
Filters
Status: Open, Classified
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Origin Data Management software versions 3.1.0, 3.1.1, 3.1.2, 3.2.0, 3.2.1
FDA Recall
Open, Classified
·Brainlab AG Olof-Palme-Str. 9 Munich Germany·Product code LLZ·February 10, 2025
Captivator Polypectomy Snare, Single-Use Polypectomy Snare consists of a flexible wire cable and loop which can be extended and retracted from the snare s flexible outer sheath using a three-ring handle. The inner diameter of the sheath is PolyGlide" Lubricant coated to provide minimal friction during extension and retraction of the loop from the sheath. When passed through an endoscope the snare can be activated to deliver a monopolar electrical current to cut and cauterize tissue with the loop.
FDA Recall
Open, Classified
·Boston Scientific Corporation·Product code FDI·July 6, 2020
Captivator/Captiflex/Sensation Short Throw Single-Use Polypectomy Snares Outer box UPN, Inner pouch UPN: M00560311 (Box 5), M00560310; M00560321 (Box 5), M00560320; M00562651 (Box 5), M00562650; M00562652 (Box 20), M00562650; M00562671 (Box 5), M00562670; M00562672 (Box 20), M00562670; M00562673 (Box 40), M00562670; M00562691 (Box 5); M00562690; M00562692 (Box 20), M00562690; M00562693 (Box 40), M00562690.
FDA Recall
Open, Classified
·Boston Scientific Corporation·Product code FDI·January 19, 2021
Captivator Single-Use Polypectomy Snares, Captiflex Single-Use Polypectomy Snares. Outer box UPN, Inner Pouch UPN: M00561311 (Box 10), M00561310 M00562301 (Box 10), M00562300; M00562321 (Box 10), M00562320; M00562341 (Box 10), M00562340; M00562451 (Box 10), M00562450; M00562401 (Box 10), M00562400; M00562402 (Box 40), M00562400; M00562422 (Box 40), M00562420; M00562471 (Box 10), M00562470.
FDA Recall
Open, Classified
·Boston Scientific Corporation·Product code FDI·January 19, 2021
Captivator Polypectomy Snare, Single-Use Polypectomy Snare consists of a flexible wire cable and loop which can be extended and retracted from the snare s flexible outer sheath using a three-ring handle. The inner diameter of the sheath is PolyGlide" Lubricant coated to provide minimal friction during extension and retraction of the loop from the sheath. When passed through an endoscope the snare can be activated to deliver a monopolar electrical current to cut and cauterize tissue with the loop.
FDA Recall
Open, Classified
·Boston Scientific Corporation·Product code FDI·July 6, 2020
Hobbs Biliary Pigtail Stent Kits (contains 3412) Catalog Number: 6027
FDA Recall
Open, Classified
·Hobbs Medical, Inc.·Product code FAD·July 29, 2022
Brand Name: Olympus Single Use Electrosurgical Snare SD-400 Product Name: Single Use Electrosurgical Snare Model/Catalog Number: SD-400U-10 Product Description: These instruments have been designed to be used with an Olympus endoscope for the removal and/or cauterization of diminutive polyps, sessile polyps, pedunculated polyps, and tissue from within the GI tract.
FDA Recall
Open, Classified
·Olympus Corporation of the Americas·Product code FDI·October 6, 2025
Hobbs Biliary Pigtail Stent Kits (containing 3412) Catalog Number: 6001
FDA Recall
Open, Classified
·Hobbs Medical, Inc.·Product code FAD·July 29, 2022
BD InLay Optima Ureteral Stent Kit Size: 4.7 Fr. x 26 cm, Ureteral Stent Kit REF 788426
FDA Recall
Open, Classified
·C.R. Bard Inc·Product code FAD·November 6, 2025
Bard InLay Optima Size: 6 Fr. x 14 cm, Ureteral Stent Kit REF 787614
FDA Recall
Open, Classified
·C.R. Bard Inc·Product code FAD·November 6, 2025
Hobbs Biliary Pigtail Stent Kits (containing 3412) Catalog Number: 6024
FDA Recall
Open, Classified
·Hobbs Medical, Inc.·Product code FAD·July 29, 2022
BD InLay Optima Ureteral Stent Kit Size: 8 Fr. x 26 cm, Ureteral Stent Kit REF 78826
FDA Recall
Open, Classified
·C.R. Bard Inc·Product code FAD·November 6, 2025
Captivator Polypectomy Snare, Single-Use Polypectomy Snare consists of a flexible wire cable and loop which can be extended and retracted from the snare s flexible outer sheath using a three-ring handle. The inner diameter of the sheath is PolyGlide" Lubricant coated to provide minimal friction during extension and retraction of the loop from the sheath. When passed through an endoscope the snare can be activated to deliver a monopolar electrical current to cut and cauterize tissue with the loop.
FDA Recall
Open, Classified
·Boston Scientific Corporation·Product code FDI·July 6, 2020
Contour VL Variable Length Ureteral Stent Set, UPN M006180155090, M006180156090, M006180156180, M006180156190
FDA Recall
Open, Classified
·Boston Scientific Corporation·Product code FAD·November 16, 2020
Hobbs Biliary Pigtail Stent Kits (containing 3412) Catalog Number: 6028
FDA Recall
Open, Classified
·Hobbs Medical, Inc.·Product code FAD·July 29, 2022
Hobbs Biliary Pigtail Stent Kits Catalog Number: 6104
FDA Recall
Open, Classified
·Hobbs Medical, Inc.·Product code FAD·July 29, 2022
Hobbs Biliary Pigtail Stent Kits Catalog Number: 6105
FDA Recall
Open, Classified
·Hobbs Medical, Inc.·Product code FAD·July 29, 2022
Hobbs Biliary Pigtail Stent Kits (containing 3412) Catalog Number:6004
FDA Recall
Open, Classified
·Hobbs Medical, Inc.·Product code FAD·July 29, 2022
Captivator Polypectomy Snare, Single-Use Polypectomy Snare consists of a flexible wire cable and loop which can be extended and retracted from the snare s flexible outer sheath using a three-ring handle. The inner diameter of the sheath is PolyGlide" Lubricant coated to provide minimal friction during extension and retraction of the loop from the sheath. When passed through an endoscope the snare can be activated to deliver a monopolar electrical current to cut and cauterize tissue with the loop.
FDA Recall
Open, Classified
·Boston Scientific Corporation·Product code FDI·July 6, 2020
Brand Name: Olympus Single Use Single Use Electrosurgical Snare SD-400 Product Name: Single Use Single Use Electrosurgical Snare Model/Catalog Number: SD-U400U-15 Product Description: These instruments have been designed to be used with an Olympus endoscope for the removal and/or cauterization of diminutive polyps, sessile polyps, pedunculated polyps, and tissue from within the GI tract.
FDA Recall
Open, Classified
·Olympus Corporation of the Americas·Product code FDI·October 6, 2025