DeRoyal Industries Inc DeRoyal Lap Appy TraceCart, REF53-1776, Rx only, non-sterile. (custom surgical kit) Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
DeRoyal Lap Appy TraceCart, REF53-1776, Rx only, non-sterile. (custom surgical kit)
Brand
DeRoyal Industries Inc
Lot Codes / Batch Numbers
Lot numbers: 13819779, 14002496, and 14356032
Products Sold
Lot numbers: 13819779, 14002496, and 14356032
DeRoyal Industries Inc is recalling DeRoyal Lap Appy TraceCart, REF53-1776, Rx only, non-sterile. (custom surgical kit) due to Surgical kits contained a recalled Endopath ETX 35 mm Endoscopic Linear Cutter White Reload/Cartridges.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Surgical kits contained a recalled Endopath ETX 35 mm Endoscopic Linear Cutter White Reload/Cartridges.
Recommended Action
Per FDA guidance
The 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.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
KY, LA
Page updated: Jan 10, 2026