Class 2 Device Recall MEDRAD(R) Hand Controller Sheath

• Date Initiated by Firm: November 05, 2012
• Date Posted: February 21, 2013
• Recall Status: Terminated on March 10, 2015
• Recall Number: Z-0870-2013
• Recall Event ID: 64329
• 510(K)Number: K050456
• Product Classification: Injector and syringe, angiographic - Product Code DXT
• Product: MEDRAD Hand Controller Sheath, Catalog number AVA 500 HCS/3010903, for cardiac catheterization procedures. The Sterile Sheath is specifically intended for use in the x-ray angiography environment to cover the Medrad Avanta Sterile Hand Controller to prevent cross contamination between patients.
• Code Information: Catalog number AVA 500 HCS/3010903 - Lot numbers D72211, DA82711, DA93131, D101091, D101681, D110591, D111961, D113341A, D120731, D101641, D82741, D93131, DA101091, DA101691, D110601, D111991, D113351, D120831A, D72251, D83011, D93151, D101101, D101701, D110611, D112061, D113351A, D120741, D72261, DA83021, DA93151, DA101101, DA101721, D110621, D112131, D113461, D120761, D72281, DA83031, DA93221, D101111, D101721, D110631, D112131A, D113461A, D120771, D72291, D83041, D93231, DA101111, D101731, D110661, D112341, D113471, D120831, D72651, DA83121, D93411, D101121, D101741, D110731, D112341A, D113471A, D120861, D72671, D83151, DA93411, DA101121, D101861, D110741, D112351, D113491, DA72681, D83651, D93421, D101131, DA101861, D110751, D112351A, D113501, DA72691, D90021, DA93421, DA101131, D101881, D110871, D112361, D120161, D72751, D90541, D93431, D101171, DA101881, D110881, D112361A, D120161A, D120891, D90561, DA93431, D101301, DA101901, D110901, D112411, D120171, D80221, D90611, D93561, D101311, D101911, D111201, D112411A, D120171A, DA80231, DA90631, D93631, DA101441, DA101931, D111221, D112421, D120181, DA80241, D90821, DA93631, D101441, D101931, D111231, D112421A, D120311, D80281, DA90831, DA100141, D101461, D101951, D111241, D112431, D120311A, D80391, D90981, D100151, DA101461, DA101951, D111261, D112431A, D120321, DA80561, D91031, D100181, D101471, D101971, D111261A, D112441, D120321A, D80631, DA91041, DA100191, DA101481, D102111, D111291, D112441A, D120331, DA80641, DA91061, DA100321, D101481, D102141, D111291A, D112481, D120341, D80871, D91071, D100331, DA101511, DA102141, D111301, D112481A, D120371, D80981, D91181, DA100341, D101511, D102151, D111301A, D112491, D120371A, DA81281, D91191, D100351, D101531, DA102151, D111311, D112501, D120381, DA81421, D91281, DA100461, DA101531, D102351, D111311A, D112621, D120381A, D81471, D91331, D100561, D101541, DA102351, D111321, D112621A, D120391, D81541, D91351, D100671, D101551, D102811, D111321A, D112631, D120451, DA81821, D91381, DA100671, DA101551, D102821, D111361, D112631A, D120511, D81971, D91561, DA100691, D101581, D102921, D120861A, D112641, D120521, D81991, D91901, D100691, DA101581, D103361, D111351, D112721, D120521A, DA82031, D92061, D100711, D101591, D103401, D111371, D112791, D120531, D82131, D92091, DA100711, DA101601, D103481, D111371A, D113071, D120541, D82141, D92111, DA100741, D101601, D103631, D111381, D113081, D120541A, D82171, D120881, D100751, D101611, D103611, D111711, D113111, D120551, D82181, D92501, D101021, D101621, D103571, D111721, D113111A, D120591, D82191, D92521, DA101021, DA101621, D103621, D111731, D113291, D120601, DA82201, DA92781, D101031, D101631, D110181, D111751, D113291A, D120671, D120881A, D92791, D101041, D101651, D110191, D111861, D113321, D120671A, D82241, D93081, DA101041, DA101651, D110321, D111871, D113321A, D120681, DA82251, D93091, D101061, D101661, D110331, D111891, D113331, D120681A, D82671, D93101, DA101061, D101671, D110351, D111921, D113331A, D120691, D82701, D93111, D101071, DA101671, D110541, D111921A, D113341, and D120721.
• Recalling Firm/ Manufacturer: Medrad Inc; 100 Global View Dr; Warrendale PA 15086
• Manufacturer Reason for Recall: The seal between the white polyethylene and the clear plastic may be missing on the Hand Controller Sheath package, resulting in a potential breach of the sterility of this accessory.
• FDA Determined Cause: Packaging
• Action: Medrad sent a Recall letter dated November 5, 2012, to all affected customers. The letter identified the product the problem and the action needed to be taken by the customer. Customer were instructed to review their inventory and quarantine any packages with an expiration date prior to April, 2017. Customers were also given the option of conducting a visual inspection on site to determine if the product should be returned. Alternatively, the customer has the option of returning the affected product. If the customer has affected product, they are instructed to contact Medrad Customer Support to make arrangements for the return and replacement of the product. For further questions please call our Customer Support Team at 1-877-229-3767.
• Quantity in Commerce: 832,175
• Distribution: Worldwide Distribution including USA nationwide.
• Total Product Life Cycle: TPLC Device Report

¹ A record in this database is created when a firm initiates a correction or removal action. The record is updated if the FDA identifies a violation and classifies the action as a recall, and it is updated for a final time when the recall is terminated. Learn more about medical device recalls.
² Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall.
³ For details about termination of a recall see Code of Federal Regulations (CFR) Title 21 §7.55.

• 510(K) Database: 510(K)s with Product Code = DXT and Original Applicant = MEDRAD, INC.