Rappel de Presource Custom Sterile Packs

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 Cardinal Health.

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
    36421
  • Classe de risque de l'événement
    Class 2
  • Numéro de l'événement
    Z-0060-2007
  • Date de publication de l'événement
    2006-10-21
  • Statut de l'événement
    Terminated
  • Pays de l'événement
  • Date de fin de l'événement
    2008-05-09
  • Source de l'événement
    USFDA
  • URL de la source de l'événement
  • 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
    Drape - Product Code LRO
  • Cause
    The cardiovascular drape may tear and/or fray at the reinforced fenestrated trough area during use.
  • Action
    Cardinal Health sent separate recall letters dated 9/27/06 via UPS next day delivery to those accounts who ordered the drapes alone and those accounts who ordered custom sterile packs and PBDS modules, informing them that the cardiovascular split drapes may tear and/or fray at the reinforced fenestrated trough area during use. The letters listed the catalog numbers and affected lot numbers of the sterile drapes, and the letters sent to the pack and module customers were accompanied by a listing of catalog numbers and work order numbers for the affected packs ordered by each account. The accounts were requested to inspect their inventory to determine if they had any of the affected product on hand; segregate the affected inventories; complete and return via fax at 847-689-9101, the enclosed acknowledgment form, indicating the number of drapes in inventory being destroyed; and contact the El Paso Customer Service Center at 915-779-3681 to order replacement product. Distributors were requested to notify their customers of the recall. An additional letter dated 10/25/06 was sent via UPS overnight delivery to 49 of the accounts, expanding the recall to include lot 06HRD110 of catalog #9158, Convertors Tiburon Cardiovascular Split Drape II, Sterile. The instructions remained the same as those in the 9/27/06 letter.

Device

  • Modèle / numéro de série
    cat #SVC13AMEMK, order #777594;  cat #SCV31OHMPJ, order #773933;  cat #SVC42OPVCG, order #774231;  cat #SCV32CPMUO, order #774845;  cat #SCV34OHTMJ, order #775103;  cat #SCV31LVLUM, order #775646;  cat #SCV19CVHHF, order #776102;  cat #SCV11ADLLD, order #776475;  cat #SCV92CBHRB, order #776785;  cat #SCV92CASIA, order #776792;  cat #SBA32GSMUL, order #777047;  cat #SCV30OHKWA, order #777171;  cat #SBA31LVLUM, order #777288;  cat #SBA35LTBLQ, order #777599;  cat #SCV44CVDEB, order #780376;  cat #SCV22OHMES, order #731809;  cat #SCV23AOSFH, order #737659;  cat #SCV43OHHRF, order #739410;  cat #SCV24CAGME, order #740765;  cat #SAN12CCKGB, order #732285;  cat #SBA13BRBSE, order #731714;  cat #SCV11CBNYP, order #732629;  cat #SCV11CESLB, order #734779;  cat #SCV11CGCPR, order #732923;  cat #SCV11CGXXB, order #735832;  cat #SCV11CJICL, order #735189;  cat #SCV11CTMUK, order #734463;  cat #SCV11DPMYG, order #732152;  cat #SCV11HEMMI, order #733639;  cat #SCV11MRCPE, order #733157;  cat #SCV11OCNYN, order #732625;  cat #SCV11OHLD2, order #732191;  cat #SCV11OHNMC, order #732446;  cat #SCV11OPLKC, order #735134;  cat #SCV11VASLB, order #737823;  cat #SCV11VLNYM, order #732656;  cat #SCV12OHYHY, order #735934, 734739, 732575;  cat #SCV13AABSV, order #732913;  cat #SCV13AMEMJ, order #732970;  cat #SCV13BBEMC, order #732070;  cat #SCV13CB767, order #732869;  cat #SCV13OHCAI, order #733777, 731664;  cat #SCV13OOBIG, order #734407;  cat #SCV14O1BGO, order #738338;  cat #SCV22OHPGA, order #735643;  cat #SCV22OOMSE, order #738400;  cat #SCV24OH20A, order #735637;  cat #SCV43DREJI, order #741763;  cat #SCV69OH17E, order #975704;  cat #SCV59HVSGJ, order #975779;  cat #SCV59OHNVM, order #976192;  cat #SCV53HTDMG, order #976853;  cat #SCV56CH11A, order #977429;  cat #SCV59MJTCW, order #977839, 978730;  cat #SCV52OH97F, order #978285;  cat #SCV41OHHIE, order #978409;  cat #SCV52HTSJE, order #978410;  cat #SCV59OHMHV, order #978523; cat #SCV11MJTJI, order 737814
  • Classification du dispositif
  • Classe de dispositif
    2
  • Dispositif implanté ?
    No
  • Distribution
    Worldwide Distribution- USA and countries of Kuwait and Australia
  • Description du dispositif
    Presource Custom Sterile Packs containing the Cardiovascular Split Drape II; the custom sterile packs were packaged with the bulk, non-sterile drapes and then the complete custom pack was sterilized; packaged by Cardinal Health Medical Products and Services, McGaw Park, IL 60085; identified by the following catalog numbers: || a) SVC13AMEMK - Sterile Open Heart Adult Pk; || b) SCV31OHMPJ - Sterile Open Heart w Drapes Pk; || c) SVC42OPVCG - Sterile Open Heart Adult Pack; || d) SCV32CPMUO - Sterile CAB 146060 Pack; || e) SCV34OHTMJ - Sterile Basin Pack; || f) SCV31LVLUM - Sterile Liver Transplant Pack; || g) SCV19CVHHF - Sterile Cardiovascular Pack; || h) SCV11ADLLD - Sterile Open Heart/Adult; || i) SCV92CBHRB - Sterile CABG Pack; || j) SCV92CASIA - Sterile Cardiovascular Pack; || k) SBA32GSMUL - Sterile General Surgery Pack; || l) SCV30OHKWA - Strl **** Open Heart Pack; || m) SBA31LVLUM - Sterile Liver Transplant Pack; || n) SBA35LTBLQ - Sterile Lung Transplant Pack; || o) SCV44CVDEB - Sterile CV Pack; || p) SCV22OHMES - Open Heart Pack; || q) SCV23AOSFH - Open Heart Part 3; || r) SCV43OHHRF - Open Heart; || s) SCV24CAGME - CABG Drape Pack; || t) SAN12CCKGB - Cardiac Pack; || u) SBA13BRBSE - Breast Reduction; || v) SCV11CBNYP - CABG G 3; || w) SCV11CESLB - C.V. Drape Pack; || x) SCV11CGCPR - CABG; || y) SCV11CGXXB - CABG Pack; || z) SCV11CJICL - Cardiac Major; || aa) SCV11CTMUK - C T Set Up; || bb) SCV11DPMYG - **** S Drape Pack; || cc) SCV11HEMMI - Open Heart A B; || dd) SCV11MRCPE - Major Cardiac; || ee) SCV11OCNYN - OH CABG; || ff) SCV11OHLD2 - Open Heart A&B; Pack; || gg) SCV11OHNMC - Open Heart; || hh) SCV11OPLKC - O P CABG; || ii) SCV11VASLB - C V Valve Drape; || jj) SCV11VLNYM - G 3 Valve; || kk) SCV12OHYHY - Graft and Linen; || ll) SCV13AABSV - Aortic Aneurysm; || mm) SCV13AMEMJ - Open Heart Pack B; || nn) SCV13BBEMC - Cardio-Thoracic Aux; || oo) SCV13CB767 - CABG; || pp) SCV13OHCAI - Open Heart Pk; || qq) SCV13OOBIG - Open Heart Drape; || rr) SCV14O1BGO - Open Heart Pack A; || ss) SCV22OHPGA - Open Heart Pack; || tt) SCV22OOMSE - Open Heart Preferred; || uu) SCV24OH20A - Open Heart Drape Pack; || vv) SCV43DREJI - Open Heart Drape Pack; || ww) SCV69OH17E - Open Heart; || xx) SCV59HVSGJ - Heart Valve Pack; || yy) SCV59OHNVM - Open Heart Pack; || zz) SCV53HTDMG - ***** Open Heart; || aaa) SCV56CH11A - Open Heart Pack; || bbb) SCV59MJTCW - Open Heart Pack; || ccc) SCV52OH97F - Open Heart Pack; || ddd) SCV41OHHIE - Open Heart Pack; || eee) SCV52HTSJE - Open Heart Pack; || fff) SCV59OHMHV - Basic Heart Pack; || ggg) SCV11MJTJI - Open Heart
  • Manufacturer

Manufacturer

  • Adresse du fabricant
    Cardinal Health, 1430 Waukegan Rd, Mc Gaw Park IL 60085-6726
  • Société-mère du fabricant (2017)
  • Source
    USFDA