24 results
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27ms
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Sources: EU EUDAMED, US FDA
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FDA Recall
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Medtronic Model 37711 Restore Neurostimulator. The Restore Neurostimulator is an implanted, rechargeable neurostimulator which provides pain management therapy.
FDA Recall
Terminated
·Medtronic Inc, Neurological & Spinal Division·Product code GZB·November 22, 2005
Percutaneous Trial Lead Kit Model 3086 (8 ch percutaneous lead). Used as part of the St. Jude Medical Neurostimulation system indicated for Spinal Chord Stimulation.
FDA Recall
Terminated
·St. Jude Medical, Inc.·Product code GZB·July 29, 2014
Percutaneous Trial Lead Kit Model 3046 (4 ch percutaneous lead). Used as part of the St. Jude Medical Neurostimulation system indicated for Spinal Chord Stimulation.
FDA Recall
Terminated
·St. Jude Medical, Inc.·Product code GZB·July 29, 2014
Swift-Lock (TM) Anchor Accessory Kit, Directions For Use Model 1192, ANS, A St. Jude Medical Company. Product is intended to be used as an accessory to the leads component of ANS SCS systems, functioning to secure the lead to the fascia or interspinous/supraspinous ligament.
FDA Recall
Terminated
·Advanced Neuromodulation Systems, Inc·Product code GZB·February 22, 2010
Medtronic SPECIFY, 3998, Lead Kit for Spinal Cord Stimulation (SCS). Manufactured at Medtronic, Inc., Villalba, Puerto Rico, USA. Contents of the inner package are STERILE. Method of sterilization: Ethylene Oxide. Model 3998 lead is an implantable, permanent lead. It is used to deliver electrical pulses to the dorsal aspect of the spinal cord. The lead consists of two polyurethane lead bodies joined to one silicone rubber paddle. The lead has two parallel rows of four platinum iridium electrodes on the distal end.
FDA Recall
Terminated
·Medtronic Neuromodulation·Product code GZB·May 21, 2008
Abbott Diabetes Care, Precision Xtra Blood Glucose Test Strips; Precision Xtra Blood Glucose & Ketone Monitoring System; Precision G3b Smartblue Blood Glucose Test Strips;
FDA Recall
Terminated
·Abbott Diabetes Care, Inc.·Product code NBW·December 22, 2010
Medtronic StimLoc Burr Hole Cover, Part Numbers: a) 3387S-40 b) 3389S-28 c) 3389S-40 d) 3391S-40 e) 3550S-01 f) 924256 g) DB-5000
FDA Recall
Open, Classified
·Medtronic Neuromodulation·Product code GXR·June 2, 2021
MUM-1 (Multiple myeloma oncogene-1), catalog number PRM352 AA; Product Usage: For In Vitro Diagnostic Use. This antibody may be used as a tool for the identification and the sub classification of lymphoid malignancies : Multiple myeloma oncogene-1 (MUM-1) is a protein encoded by MUM-1 gene. MUM-1 protein is expressed in the nuclei and cytoplasm of plasma cells and a small percentage of germinal center (GC) B-cells located in the light zone. MUM-1 [BC5] labels MUM-1protein in centrocytes and their progeny, plasma cells, activated T-cells and a wide spectrum of hematolymphoid neoplasms derived from these cells. MUM-1 has been reported to play an important role in mediating B-cell activation and differentiation.
FDA Recall
Terminated
·Biocare Medical Llc·Product code NJT·December 12, 2014
KliniTray Platte Faxitron ,groB "R" sterile. Tissue resection margin examination board/large Model Number: 2001155-F The medical device KliniTrayTM is a system for the precise monitoring, recording and visualization of alignment during surgical procedures. It ensures the exact orientation and positioning of tissue to be removed in the patient's body, enabling improved surgical precision and patient safety.
FDA Recall
Open, Classified
·Klinika Mdical Gmb Achtzehnmorgenweg 6 Usingen Germany·Product code FMH·April 4, 2025
KliniTray. KlinioTray. Tissue resection margin examination board/small. Model Number: 2001105-F The medical device KliniTrayTM is a system for the precise monitoring, recording and visualization of alignment during surgical procedures. It ensures the exact orientation and positioning of tissue to be removed in the patient's body, enabling improved surgical precision and patient safety.
FDA Recall
Open, Classified
·Klinika Mdical Gmb Achtzehnmorgenweg 6 Usingen Germany·Product code FMH·April 4, 2025
Contour VL Ureteral Stent Set 6FX22-30CM with .035 Sensor UPN: M006180156080
FDA Recall
Open, Classified
·Boston Scientific·Product code EZB·March 9, 2020
Percuflex Plus Ureteral Stent Set 7FX24CM with .035 Sensor UPN: M006175272080 (edited 1/13/2021)
FDA Recall
Open, Classified
·Boston Scientific·Product code EZB·March 9, 2020
Sensor Nitinol Wire with Hydrophilic Tip .0383CM FLEX ANG/150CM UPN: M0066703101 box 5 UPN: M0066703100 single unit
FDA Recall
Open, Classified
·Boston Scientific·Product code EZB·March 9, 2020
Percuflex Plus Ureteral Stent Set 6FX24CM with .038 Sensor UPN: M006175262110
FDA Recall
Open, Classified
·Boston Scientific·Product code EZB·March 9, 2020
Brand Name: 3B Medical, Inc. Product Name: Ultrasoft Oxygen Cannula, 12 Foot Model / Catalog Number: O2U2012 Lot Number: 20170403 Product Description: Nasal Cannulas for use with Oxygen Concentrators
FDA Recall
Open, Classified
·3B Medical, Inc.
203 Avenue A Nw Ste 300
Winter Haven FL 33881-4540·Product code BZB·November 27, 2024
Cook PTFE Wire Guide with 3 cm flexible tip, to establish a tract for ureteral/renal access, .038", 145 cm; sterile; Order/Ref number 638413.
FDA Recall
Terminated
·Cook Urological, Inc.·Product code EZB·June 12, 2007
Stretch VL Ureteral Stent Set 7FX22-30CM with .035 Sensor UPN: M006185157080
FDA Recall
Open, Classified
·Boston Scientific·Product code EZB·March 9, 2020
Percuflex Plus Ureteral Stent Set 6FX26CM with .038 Sensor UPN: M006175263110
FDA Recall
Open, Classified
·Boston Scientific·Product code EZB·March 9, 2020
Sensor Nitinol Wire with Hydrophilic Tip .035 3CM FLEX /150CM UPN: M0066703061 box 5 UPN: M0066703060 single unit
FDA Recall
Open, Classified
·Boston Scientific·Product code EZB·March 9, 2020
Stretch VL Ureteral Stent Set 6FX22- 30CM with .035 Sensor UPN: M006185156080
FDA Recall
Open, Classified
·Boston Scientific·Product code EZB·March 9, 2020