Health product recall

Presource Procedure Packs

Last updated

Summary

Product
Presource Procedure Packs
Issue
Medical devices - Device compatibility
What to do

Quarantine affected inventory, affix supplied warning label (to discard component), return reply form. 

Audience
Healthcare

Affected products

Affected products Lot or Serial number Model or Catalogue number
Presource Procedure Packs 656401 795238 718556 713939 711087 631781 696297 786839 715657 SAN30LPGBB SBA30LBNHD SBA30LBYCB

Issue

Cardinal Health was recently informed of a field action correction from Becton Dickinson (bd) concerning the manometer bottom assembly. The correction is being issued due to complaints and mating issues from the manometer. After reviewing the potential impact of this recall on Presource Procedure Packs, Cardinal Health is initiating an urgent medical device correction on specific lots of Presource packs produced containing the affected bd manometer bottom assembly component and lot number(s).

Recall start date: May 20, 2022

Additional information

Details
Original published date:
Alert / recall type
Health product recall
Category
Health products - Medical devices - General hospital and personal use
Companies

Cardinal Health

3651 Birchwood Drive, Waukegan, Illinois, United States, 60085

Published by
Health Canada
Audience
Healthcare
Recall class
Type II
Identification number
RA-64208

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