Events

Rappel de Device Recall ECHELON 60mm Endoscopic Linear Cutter Reloads Black

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 Ethicon Endo-Surgery Inc.

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
    65330
  • Classe de risque de l'événement
    Class 2
  • Numéro de l'événement
    Z-1530-2013
  • Date de mise en oeuvre de l'événement
    2013-05-13
  • Date de publication de l'événement
    2013-06-11
  • Statut de l'événement
    Terminated
  • Pays de l'événement
    United States
  • Date de fin de l'événement
    2014-02-11
  • Source de l'événement
    USFDA
  • URL de la source de l'événement
    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=118570
  • 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
    Staple, implantable - Product Code GDW
  • Cause
    Ethicon endo-surgery is initiating a voluntary worldwide recall for echelon 60mm black reload (ecr60t) due to the potential for incomplete staple line formation from reload damage during the firing sequence.
  • Action
    Ethicon sent a Urgent: Medical Device Recall letter dated May 29, 2013, to all affected customers. The letter identified the product the problem and the action to be taken by the customer. Customers were instructed 1.To examine your inventory immediately to determine if you have affected product manufactured by Ethicon and remove the affected product(s). See Attachment A for assistance in identifying affected product. 2. Complete the Business Reply Form (BRF) Attachment C and fax or email it to Stericycle at 1-888-943-4190. Please reference Event 4706. If you have product to be returned, keep a copy of this form for your records. Your JJHCS number has been pre-populated on the BRF. Replacement product will be issued for all returned recalled product. 3. All affected product must be returned by August 30, 2013, to receive replacement product. To return affected product, photocopy your completed Business Reply Form, placeit in the box with your product, and affix the pre-printed UPS shipping label to return to Stericycle. Returned ECHELON 60mm Black Reload (ECR60T) will be replaced with corrected ECHELON 60mm Black Reload (ECR60T) as soon as supply becomes available. 4. If you do not have affected product in your inventory, you should still complete and return the Business Reply Form, indicating you have no affected product. 5. Please share this information with all of the appropriate staff at your facility. 6. If you need assistance identifying an alternative product code, please speak directly with your Ethicon Sales Representative. If you need clinical or product support, please contact your local sales representative or call our Customer Support Center, 1-877-ETHICON (877-384-4266 OPTION 6 to speak with a registered nurse). If you need additional shipping labels or a communications package, contact the Stericycle support center at 1-888-943-2397 and reference Event 4706.

Device

Device Recall ECHELON 60mm Endoscopic Linear Cutter Reloads Black
  • Modèle / numéro de série
    The following lot numbers and associated expiration dates are affected by this recall: J4AY8Z 5/15/2013, J4C00J 6/15/2013, J4C87R 7/15/2013, J4CC1F 8/15/2013, J4CD2X 8/15/2013, J4CF3D 9/15/2013, J4CJ0E 9/15/2013, J4CJ78 9/15/2013, J4CK2P 9/15/2013, J4CM9X 10/15/2013, J4CR2H 10/15/2013, J4CT5H 11/15/2013, J4CU86 11/15/2013, J4CV1W 11/15/2013, J4CV5H 11/15/2013, K4C149 12/15/2013, K4C17W 12/15/2013, K4C33U 12/15/2013, K4C41C 12/15/2013, K4C600 1/15/2014, K4C64A 1/15/2014, 4C728 1/15/2014,  K4C82K 1/15/2014, K4C88F 1/15/2014, K4C94W 1/15/2014, K4CC0L 2/15/2014, CC8L 2/15/2014, K4CD1E 2/15/2014, K4CF1P 2/15/2014, K4CF5D 2/15/2014, K4CG18 3/15/2014, K4CG4J 3/15/2014, K4CG8P 3/15/2014, K4CH44 3/15/2014, K4CK0W 3/15/2014.
  • Classification du dispositif
    General and Plastic Surgery Devices
  • Classe de dispositif
    2
  • Dispositif implanté ?
    Yes
  • Distribution
    Worldwide Distribution - US Nationwide all fifty states and including the countries of Canada, Belgium, India, Malaysia, Saudi Arabia, Brazil, Israel, Mexico, Singapore, Jordan, New Zealand, Taiwan, Chile, Korea, Puerto Rico, Turkey, Columbia, Kuwait, Qatar, United Arab Emirates, Egypt, Lebanon and Russia.
  • Description du dispositif
    ECHELON 60mm Endoscopic Linear Cutter Reloads Black in Flexible Blister pack with Tyvek lid. || The ECHELON and ECHELON FLEX families of Endoscopic Linear Cutters (articulating and straight) are sterile, single patient use instruments that simultaneously cut and staple tissue. There are six staggered rows of staples, three on either side of the cut line. The ECHELON 60 instruments have a staple line that is approximately 60 mm long and a cut line that is approximately 57 mm long. The shaft can rotate freely in both directions and an articulation mechanism on articulating instruments enables bending the distal portion of the shaft to facilitate lateral access of the operative site. The instruments are shipped without a reload and must be loaded prior to use. A staple retaining cap on the reload protects the staple leg points during shipping and transportation. The instruments'¿" lock-out feature is designed to prevent a used reload from being refired.
  • Manufacturer
    Ethicon Endo-Surgery Inc

Manufacturer

Ethicon Endo-Surgery Inc
  • Adresse du fabricant
    Ethicon Endo-Surgery Inc, 4545 Creek Rd, Cincinnati OH 45242-2803
  • Société-mère du fabricant (2017)
    Johnson & Johnson
  • Source
    USFDA