ClearanceBrief
Recall Z-0089-2018 ยท OGE Epidural Anesthesia Kit

Epimed International

TUOHY Epidural Needle, 20g x 3.5in(8.9cm) TW, 10 units, Calibrated, Plastic Hub, Fixed Wing, Sterile, Rx only

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.
Quantity263 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

K030562TUOHY EPIDURAL NEEDLE
Epimed International, Inc., Apr 3, 2003