42 results
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14ms
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Sources: EU EUDAMED, US FDA
Filters
Status: Open, Classified
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Penner Pacific Bathing Spa, Model Numbers 360010-2WT, 360010-1, 370000-1W, 360010-1WT, 362010-1, 370000-1WL, 360010-1L, 360010-1W, 360010-XWTL, 370000-XWL, 360010-1WTL, 360010-XWT, 360010-2, 370000-2W, 360010-2L, 370000-2WL, 360010-X, 370000-XW, 360010-2W, 362010-2, 360010, 37000-XWL, 362010-X, 362010-XL, 362010-1L, 360010-XL, 37000-1W, 360010-XW, 3700000-1W, 362010-2L, 36010-XWT, 370000-1L, 360010-2WT, 360000-1, 360010-XWSB, 360010-XLSB
FDA Recall
Open, Classified
·Penner Patient Care, Inc.·Product code ILJ·August 13, 2025
Brand Name: Meridian Angled Awl Fixed Product Name: Angled Awl Fixed Model/Catalog Number: RA2-003015 Product Description: Surgical Awl Component: No
FDA Recall
Open, Classified
·SEASPINE ORTHOPEDICS CORPORATION·Product code HWJ·June 4, 2024
LIF AMP, Adjustable Awl, REF 117-165, Part of the AMP System. Used with Spine Lateral Interbody Systems, IdentiTi LIF, Transcend LIF and Battalion LLIF,
FDA Recall
Open, Classified
·Alphatec Spine, Inc. 1950 Camino Vida Roble·Product code HWJ·July 7, 2023
CD HORIZON Spinal System Solera Awl Tip Tap, REF NAV2006K
FDA Recall
Open, Classified
·Medtronic Sofamor Danek USA, Inc·Product code OLO·July 12, 2023
TiBrid Stand Alone Intervertebral Body Fusion Device, SA Angled Punch Awl, Sizes: 30 degree, 45 degree and 60 degree.
FDA Recall
Open, Classified
·Product code OVD·July 15, 2024
24K Premium Lense, Distributed by Updream Inc.
FDA Recall
Open, Classified
·Ontact Inc 10944 Playa Del Sol·Product code MVN·March 20, 2024
GORE CARDIOFORM ASD Occluder. cardiovascular implant.
FDA Recall
Open, Classified
·W L Gore & Associates, Inc.·Product code MLV·September 21, 2022
Gore Molding & Occlusion Balloon Catheter, REF Catalogue Number MOB37, SN XXXXXXXX, 10 mm - 37 m 10 Fr, Guidewire Compatibility 0.035", STERILE EO, CE2797, UDI: (00)733132639489
FDA Recall
Open, Classified
·W. L. Gore & Associates Inc.·Product code MJN·July 12, 2021
Gore Propaten Vascular Graft configured for Pediatric Shunt, Diameter 5 mm, Length 10 cm, Rx Only, Sterile EO, for the following Reference numbers: HPT050010 UDI: (01)00733132606320 HPT050010A UDI: (01)00733132606337
FDA Recall
Open, Classified
·W L Gore & Associates, Inc.·Product code DSY·May 12, 2021
Heparin, GORE VIABAHN VBX, BALLOON EXPANDABLE ENDOPROTHESIS, REF BXAL085902E, 8 MM X 59 MM 8 Fr, LARGE BALLOON EXPANDLBE, Nominal Stent Diameter 8 mm, Max Post-Dilated Stent Diameter 16 mm, UDI:
FDA Recall
Open, Classified
·W L Gore & Associates, Inc.·Product code PRL·September 7, 2021
REF/Catalogue Number GSXE0020, GORE CARDIOFORM SEPTAL OCCLUDER 20 mm Diameter, Catheter Working Length 75 cm, Delivery Profile 10 Fr, STERILE EO, Rx Only, UDI: 00733132617630 *Not distributed within the US
FDA Recall
Open, Classified
·W L Gore & Associates, Inc.·Product code MLV·September 2, 2021
REF/Catalogue Number GSXE0025, GORE CARDIOFORM SEPTAL OCCLUDER 25 mm Diameter, Catheter Working Length 75 cm, Delivery Profile 10 Fr, STERILE EO, Rx Only, UDI: 00733132617647 *Not distributed within the US
FDA Recall
Open, Classified
·W L Gore & Associates, Inc.·Product code MLV·September 2, 2021
REF/Catalogue Number GSX0025A, GORE CARDIOFORM SEPTAL OCCLUDER 25 mm Diameter, Catheter Working Length 75 cm, Delivery Profile 10 Fr, STERILE EO, Rx Only, UDI: 00733132631025 *Not distributed within the US
FDA Recall
Open, Classified
·W L Gore & Associates, Inc.·Product code MLV·September 2, 2021
GORE ACUSEAL Vascular Graft, REF: ECH050020J, ECH050020W, ECH050050J, ECH050050W, ECH060010A, ECH060020A, ECH060020J, ECH060020W, ECH060040, ECH060040A, ECH060040W, ECH060050A, ECH060050J, ECH460045A, ECH460045J, ECH470045, ECH470045A; used with Instructions for Use.
FDA Recall
Open, Classified
·W L Gore & Associates, Inc.·Product code DSY·August 26, 2025
Heparin, Gore Viabahn VBX, Balloon Expandable Endoprosthesis, for the following Reference numbers: United States: BXB055902C, BXB063902C, BXB065902C, BXB067902C, BXB073902C, BXB075902C, BXB077902C, BXB083902C, BXB085902C, BXB087902C, BXB093902C, BXB095902C, BXB097902C *For Clinical use.
FDA Recall
Open, Classified
·W L Gore & Associates, Inc.·Product code PRL·July 1, 2024
REF/Catalogue Number GSX0020A, GORE CARDIOFORM SEPTAL OCCLUDER 20 mm Diameter, Catheter Working Length 75 cm, Delivery Profile 10 Fr, STERILE EO, Rx Only, UDI: 00733132631018
FDA Recall
Open, Classified
·W L Gore & Associates, Inc.·Product code MLV·September 2, 2021
REF/Catalogue Number GSXE0025B, GORE CARDIOFORM SEPTAL OCCLUDER 25 mm Diameter, Catheter Working Length 75 cm, Delivery Profile 10 Fr, STERILE EO, Rx Only, UDI: 00733132620111 *Not distributed within the US
FDA Recall
Open, Classified
·W L Gore & Associates, Inc.·Product code MLV·September 2, 2021
REF/Catalogue Number GSXE0030B, GORE CARDIOFORM SEPTAL OCCLUDER 30 mm Diameter, Catheter Working Length 75 cm, Delivery Profile 10 Fr, STERILE EO, Rx Only, UDI: 00733132620128 *Not distributed within the US
FDA Recall
Open, Classified
·W L Gore & Associates, Inc.·Product code MLV·September 2, 2021
REF/Catalogue Number GSX0030H, GORE CARDIOFORM SEPTAL OCCLUDER 30 mm Diameter, Catheter Working Length 75 cm, Delivery Profile 10 Fr, STERILE EO, Rx Only, UDI: 00733132648948 *Not distributed within the US
FDA Recall
Open, Classified
·W L Gore & Associates, Inc.·Product code MLV·September 2, 2021
REF/Catalogue Number GSX0030A, GORE CARDIOFORM SEPTAL OCCLUDER 30 mm Diameter, Catheter Working Length 75 cm, Delivery Profile 10 Fr, STERILE EO, Rx Only, UDI: 00733132631032
FDA Recall
Open, Classified
·W L Gore & Associates, Inc.·Product code MLV·September 2, 2021