Urgent recall of specific lots of DELTA XTEND™ Reverse Shoulder System Modular Centered and Eccentric Epiphysis Implants due to out-of-specification manufacturing issue
Healthcare professional
Medical devices
20 October 2017
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Johnson & Johnson Pte Ltd would like to inform healthcare professionals of the urgent recall of specific lots of DELTA XTEND™ Reverse Shoulder System Modular Centered and Eccentric Epiphysis Implants due to out-of-specification manufacturing issue. This is related to the circularity of the cylinder which may interfere with the proper assembly of the epiphysis and the stem. If used, this may lead to surgical delay or corrective reoperation in patients. Healthcare professionals are advised to cease use of all affected devices. Please refer to the letter for details.
Only abstracts of the Dear Healthcare Professional Letters (DHCPL) are provided on this website. Details of these letters can be found in the MOH Alert System, which is accessible via the Health Professionals Portal (HPP), a one-stop portal for all healthcare professionals in Singapore. Dentists, medical doctors and pharmacists may access HPP at https://hpp.moh.gov.sg and follow the procedures below to access the MOH Alert system.
Step 1: Select your profession under ‘For Healthcare Professionals’.
Step 2: Click on ‘Useful links’.
Step 3: Click on ‘MOH Alert’ and log in via Singpass.
Step 4: Click on ‘Drug Alerts’ or ‘Med Device Alerts’ to view the DHCPLs.
