ClearanceBrief
Recall Z-0198-2009 ยท KDD Kit, Surgical Instrument, Disposable

DeRoyal Industries Inc

DeRoyal Lap Chole Tray, REF 89-4823.06, Rx, Sterile EO. (custom surgical kit)

DateNov 7, 2008 (initiated Oct 1, 2008)
StatusTerminated
ReasonSurgical kits contained a recalled Endopath ETX 35 mm Endoscopic Linear Cutter White Reload/Cartridges.
Root causeNonconforming Material/Component
ActionThe firm sent out recall notices to their sales representatives, the distributors, and the hospitals addressed to the Recall Coordinator/OR Supervisor on 10/2/08. These notices stated that the recalling firm's sales representatives would perform the field correction in lieu of returning the kits. Contact DeRoyal Industries, Inc. at 1-865-362-6157 for assistance.
Quantity30 kits
DistributionLA & KY
FDA recordOpen on fda.gov

510(k) clearances named in this recall

This recall record lists no 510(k) number.