ClearanceBrief
Recall Z-0088-2018 ยท OGE Epidural Anesthesia Kit

Epimed International

COUDE Blunt Nerve Block Needle, 10 units, 0.71mm (22 Ga) x 152mm, Each Unit Contains One Blunt Nerve Block Needle and One Wing, Sterile

DateJul 24, 2017
StatusTerminated
ReasonPotential for partially incomplete seal of product, impacting sterility.
Root causeEmployee error
ActionConsignees were contacted 07/24/2017 via email and phone, notifying them of the recall. Consignees were asked to contact the recalling firm to report the number of affected product on hand. A second, updated recall notification was sent on 08/04/2017. Instructions included to examine inventory and quarantine any affected product, contact Epimed to arrange return/credit of the affected product, and complete and return the response form.
Quantity300 units
DistributionDomestic: AR, CA, IA, IN, KY, LA, MI, NY, OH, OR, TN, TX, & WA. Foreign: Canada, Czech Republic, Germany ,& Turkey.
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K041843PENCIL POINT NEEDLE
Epimed International, Inc., Aug 24, 2004