ClearanceBrief
Recall Z-1270-03 ยท KDC Instrument, Surgical, Disposable

International Surgical Supply, Inc.

ETHICON brand surgical device with an added label with the labeling Manufactured by: MedSurg Solutions, 3025 Harbor Lane suite 104 Plymouth, MN 55447 and/or another additional label which states MEDSURG 3025 Harbor Lane, Suite 104, Plymouth, MN 55447 Steriliation Date:. The product labels also state the following firm: ETHICON, INC. SOMERVILLE, N.J. 08876-0151 The product described on label is a:

DateSep 23, 2003 (initiated Sep 3, 2003)
StatusTerminated
ReasonVarious Sterile Expired and Non-expired Ethicon brand surgical devices were resterilized without adequate validations and distributed.
Root causeOther
ActionThe firm sent an e-mail recall notification and request for response on 9/3/2003, to the one direct account in Minnesota requesting quarantine and return of product and also subrecall down to the hospital/health professional level.
Quantity8
DistributionProduct was distributed to a direct consignee/distributor in Minnesota and also directly to the only two hospital/health professional accounts involved both in Tennessee.
FDA recordOpen on fda.gov

510(k) clearances named in this recall

This recall record lists no 510(k) number.