Product Wiki · Recalls · Health Canada — Medical Devices

Baxter Peritoneal Dialysis (PD) Transfer Sets, Titanium Adapters… — recall 52652

Health Canada — Medical Devices · Canada · 2015-01-29 · Type II

As described by Health Canada — Medical Devices: Baxter Peritoneal Dialysis (PD) Transfer Sets, Titanium Adapters; Disconnect Caps and Connection Shield Products (2014-12-18)

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Agency
Health Canada — Medical Devices
Recall identifier
52652
Date of alert
2015-01-29
Country / jurisdiction
Canada
Risk level
Type II
Risk type
recall
Product category
Medical devices
Product type
Medical devices
Notice status
Archived by the issuing authority — kept for reference
Reported risk: Baxter is sending an important safety update to the instructions for use for Baxter Peritoneal Dialysis (PD) transfer sets, titanium adapters; disconnect caps and connection shield product codes. Specifically, Baxter is adding contraindication statements to address iodine allergy for Baxter's PD products which contain iodine (i.e., povidone iodine) or for which iodine use is recommended. There is no product hold or physical removal of devices from the field associated with this action.
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/baxter-peritoneal-dialysis-pd-

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