Events

Rappel de Medtronic Intrathecal Catheter Spinal Segment Revision Kit, 8598A.

Selon U.S. Food and Drug Administration, ce/cet/cette rappel concerne un dispositif en/au/aux/à United States qui a été fabriqué par Medtronic, Inc. - Neuromodulation.

Qu'est-ce que c'est?

Une correction ou un retrait opéré par un fabricant afin de répondre à un problème causé par un dispositif médical. Les rappels surviennent lorsqu'un dispositif médical est défectueux, lorsqu'il pourrait poser un risque pour la santé, ou les deux à la fois.

En savoir plus sur les données ici
  • Type d'événement
    Recall
  • ID de l'événement
    57024
  • Classe de risque de l'événement
    Class 2
  • Numéro de l'événement
    Z-0335-2011
  • Date de publication de l'événement
    2010-11-09
  • Statut de l'événement
    Terminated
  • Pays de l'événement
    United States
  • Date de fin de l'événement
    2011-12-10
  • Source de l'événement
    USFDA
  • URL de la source de l'événement
    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=95196
  • Notes / Alertes
    U.S. data is current through June 2018. All of the data comes from the U.S. Food and Drug Administration, except for the category Manufacturer Parent Company.
    The Parent Company was added by ICIJ.
    The parent company information is based on 2017 public records.
  • Notes supplémentaires dans les données
    Pump, infusion, implanted, programmable - Product Code LKK
  • Cause
    Medtronic is recalling specific lots of model 8731sc intrathecal catheter kits and model 8598a intrathecal catheter spinal revision kits because there is the potential that the 11.4 cm introducer needles within these kits may exceed usp requirements for bacterial endotoxin.
  • Action
    Medtronica sent an "Urgent: Medical Device Recall" letter, dated September 2010, was sent to medical facilities/customers beginning September 29, 2010. The letter described the issue, identified affected product, requested that unused inventory be segregated and returned to Medtronic Neuromodulation per the enclosed Product Return Instructions form. A Recall Reply Card was also asked to be returned. Additionally an "Urgent: Medical Device Recall" letter was addressed to Healthcare Providers/customers to inform them of the recall of the Catheter and Revision Kits, identified patients by means of registration information, Informed them of the issue with the needle inside the kits, and requested they stop using the specific lots and to monitor any patients for symptoms. If you have any questions or comments, please contact Medtronic Neuromodulation Technical Services at 1-800-707-0933.

Device

Medtronic Intrathecal Catheter Spinal Segment Revision Kit, 8598A.
  • Modèle / numéro de série
    Lot No.: 0203951576, 0203961984, 0203967623, 0203968380, 0203972121, 0203975643, 0203975644, 0203977013, 0203986903, 0203986904, 0203986905, 0203986906, 0203986907, 0203986908, 0203987226, 0203987613, 0203987614, 0203987927, 0203992275, 0203994418, 0204000009, 0204008277, 0204013891, 0204013892, 0204013893, 0204021022, 0204025158, 0204032708, 0204036999, 0204077467, 0204086950, 0204086951, 0204086952, 0204086953, 0204093420, 0204100469, 0204100472, 0204106116, 0204127318, 0204128817, 0204133515, 0204133516, 0204133517, 0204133545, 0204133546, 0204133547, 0204135762, 0204135763, 0204150859, 0204151516, 0204151517, 0204152813, 0204153722, 0204164696, 0204168597, N258157001, N258157002, N258157003, N258157004, N258157005, N258158001, N258158002, N258158003, N258158004, N258158005, N258158006, N258158007, N258158008, N258158009, N258158010, N258158011, N258158012, N258158013, N258158014, N258158015, N258162001, N258162002, N258162003, N258162004, N258162005, N258162006, N258162007, N258162008, N258162009, N258162010, N258163001, N258163002, N258163003, N258163004, N258163005, N258320001, N258320002, N258320003, N258320004, N258320005, N258327001, N258327002, N258327003, N258327004, N258327005, N258327006, N258327007, N258327008, N258327009, N258327010, N258327011, N258327012, N258327013, N258327014, N258327015, N258329001, N258329002, N258329003, N258329004, N258329005, N258329006, N258329007, N258329008, N258329009, N258329010, N258329011, N258329012, N258329013, N258329014, N258329015, N258329016, N258329017, N258329018, N258329019, N258329020, N258330001, N258330002, N258330003, N258330004, N258330005, N258981001, N258981002, N258981003, N258981004, N258981005, N258981006, N258981007, N258981008, N258981009, N258981010, N258981011, N258981012, N258981013, N258981014, N258981015, N258985001, N258985002, N258985003, N258985004, N258985005, N258985006, N258985007, N258985008, N258985009, N258985010, N258985011, N258985012, N258985013, N258985014, N258985015, N259066001, N259066002, N259066003, N259066004, N259066005, N259425001, N259425002, N259425003, N259425004, N259425005, N259425006, N259425007, N259425008, N259425009, N259425010, N259898001, N259898002, N259898003, N259898004, N259898005, N259898006, N259898007, N259898008, N259898009, N259898010, N259898011, N259900001, N259900002, N259900003, N259900004, N260559001, N260560001, N260560002, N260560003, N260560004, N260560005, N260560006, N260560007, N260560008, N260560009, N260560010, N260560011, N260560012, N260560013, N260560014, N260941001, N260941002, N260941003, N260941004, N260941005, N260946001, N260946002, N260946003, N260946004, N260946005, N260946006, N260946007, N260946008, N260946009, N260946010, N261572001, N261572002, N261572003, N261572004, N261572005, N261572006, N261572007, N261572008, N261572009, N261572010, N261572011, N261572012, N261572013, N261572014, N261572015, N262484001, N262484002, N262484003, N262484004, N262484005, N262484006, N262484007, N262484008, N262484009, N262484010, N262484011, N262484012, N262484013, N262484014, N262484015, N263403001, N263403002, N263403003, N263403004, N263403005, N263403006, N263403007, N263403008, N263403009, N263405001, N263405002, N263405003, N263405004, N263405005, N263405006, N263408001, N263893001, N263893002, N263893003, N263893004, N263893005, N263893006, N263893007, N263893008, N263893009, N263893010, N263893011, N263893012, N263893013, N263893014, N263895001, N263895002, N263895003, N263895004, N263895005, N263895006, N263895007, N263895008, N263895009, N263895010, N263895011, N263895012, N263895013, N263895014, N263895015, N264167001, N264167002, N264167003, N264167004, N264167005, N264167006, N264167007, N264167008, N264167009, N264167010, N264167011, N264167012, N264167013, N264167014, N264167015, N265426001, N265426002, N265426003, N265426004, N265426005, N265426006, N265426007, N265426008, N265426009, N265426010, N265426011, N265426012, N265426013, N265426014, N265426015, N265429001, N265429002, N265429003, N265429004, N265429005, N265429006, N265429007, N265429008, N265429009, N265429010, N265429011, N265429012, N265429013, N265429014, N265429015, N265940001, N265940002, N265940003, N265940004, N265940005, N265940006, N265940007, N265940008, N265940009, N265940010, N268412001, N268412002, N268412003, N268412004, N268412005, N268415001, N268415002, N268415003, N268415004, N268415005, N268415006, N268415007, N268415008, N268415009, N268415010, N268415011, N268415012, N268415013, N268415014, N268415015, N268416001, N268416002, N268416003, N268416004, N268416005, N268416006, N268416007, N268416008, N268416009, N268416010, N268416011, N268416012, N268416013, N268416014, N268416015, N268417001, N268417002, N268417003, N268417004, N268417005, N268417006, N268417007, N268417008, N268417009, N268417010, N268417011, N268417012, N268417013, N268417014, N268417015, N268419001, N268419002, N268419003, N268419004, N268419005, N268424001, N268424002, N268424003, N268424004, N268424005, N268424006, N268424007, N268424008, N268424009, N268424010.
  • Classification du dispositif
    General Hospital and Personal Use Devices
  • Classe de dispositif
    3
  • Dispositif implanté ?
    Yes
  • Distribution
    AL, CA, CO, CT, FL, GA, HI, ID. IL, IN, KS, KY, MA, MD, MI, MN, MO, MT, NC, NJ, NM, NY, OH, OR, PA, SC, SD, TN, TX, VA, WA, WI, WV, WY. OUS to include: Argentina, Austria, Belgium, Canada, Chile, Czech Republic, France, Germany, Greece, Hungary, Ireland, Israel, Italy, San Marino, Jordan, Lithuania, Netherlands, Norway, Saudi Arabia, Slovenia, South Africa, Spain, Sweden, Switzerland, Tunisia, United Arab Emirates, United Kingdom.
  • Description du dispositif
    Medtronic Intrathecal Catheter Spinal Segment Revision Kit, 8598A. Method of Sterilization: Ethylene Oxide. Manufacturer Medtronic, Inc., 710 Medtronic Parkway, Minneapolis, MN 55432-5604 USA. The Medtronic Model 8598A Spinal Segment Revision Kit is used when a revision to the spinal segment of a Model 8731 or Model 8731SC catheter is required. The catheter is part of an infusion system that stores and delivers parenteral drugs to the intrathecal space. The implanted infusion system components consist of a Medtronic pump and a Model 8731 or Model 8731SC catheter. The catheter connects to the pump at the catheter port. || To deliver parenteral drugs to the intrathecal space. The needle is used to facilitate the placement of the catheter. The needle is inserted percutaneously into the intrathecal. The needle stylet is then removed to confirm the needle placement through observing backflow of cerebrospinal fluid (CSF) through the needle. The needle stylet prevents tissue coring and also minimizes loss of CSF. The spinal segment tip of the catheter is inserted through the needle until the catheter is advanced to the desired location. Once the catheter position is verified through fluoroscopy, the needle is carefully removed and discarded.
  • Manufacturer
    Medtronic, Inc. - Neuromodulation

Manufacturer

Medtronic, Inc. - Neuromodulation
  • Adresse du fabricant
    Medtronic, Inc. - Neuromodulation, 7000 Central Ave NE, Minneapolis MN 55432-3568
  • Société-mère du fabricant (2017)
    Medtronic plc
  • Commentaire du fabricant
    “If our surveillance systems identify a potential performance issue, our personnel promptly evaluate the problem, including, when appropriate, conducting root cause investigations and internal testing to assess whether the product continues to meet specifications and defined performance criteria,” Medtronic told ICIJ in a statement. “In some cases, based on this evaluation, Medtronic may determine that a recall is necessary.” The company said that it communicates with healthcare providers and/or patients and provide recommendations to address such issues. Medtronic noted that these communications can include letters, emails, calls, press releases, physician notifications and social media postings, as well as informing the FDA and other regulators of the actions.
  • Source
    USFDA