Regard custom surgical pack labeled as "LAP - FLOL LADY OF ANGELS" including recalled Stryker part numbers 0620 040 660 Pneumosure High Flow II Tubeset, 0620 040 690 Pneumosure Heated Tubeset with RTP and 0620 040 680 Pneumosure High Flow Tubeset with RTP.
Recall
- Recall Number
- Z-2220-2019
- Event Number
- 82499
- FEI Number
- 3004513970
- Product Code
- KDD
- Status
- Open, Classified
- Root Cause
- Nonconforming Material/Component
- Initiated
- March 21, 2019
- Address
- 2909 N Neergard Ave, ROi Consolidated Service Center (CSC), Springfield, MO, 65803-6317
Description
Regard custom surgical pack labeled as "LAP - FLOL LADY OF ANGELS" including recalled Stryker part numbers 0620 040 660 Pneumosure High Flow II Tubeset, 0620 040 690 Pneumosure Heated Tubeset with RTP and 0620 040 680 Pneumosure High Flow Tubeset with RTP.
Resource Optimization & Innovation (ROi) has received a recall notice from Stryker regarding tube sets potentially detaching from the cassette, which can lead to leaking gas or a hissing sound.
ROi, Consolidated Service Center ROi, notified customers on about 03/21/2019. Each email included a copy of the ROi "MEDICAL DEVCIE RECALL NOTIFICATION" dated March 21, 2019 as well as the Stryker recall notification dated March 7, 2019. ROi notification letter instructed customers to review inventory to determine if the affected ROi Custom Pack item and lot numbers are in inventory, quarantine all affected packs on hand, and notify ROi of the number of each affected lot on hand by completing and returning "Attachment A" via email to [email protected]. Supplemental labels for affected packs will be issued, which will instruct the end user to remove the affected Stryker component(s) and to use single sterile replacement product form inventory. If there is not any affected inventory on hand, customers are requested to still return Attachment A indicating "0" affected inventory at their facility.
Distributed to LA and MO
261 packs