Canadian data is current through March 2018. All of the data comes from Health Canada, except for the categories Manufacturer Parent Company and Product Classification.
The Parent Company and the Product Classification were added by ICIJ.
The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of recall data from the U.S. and Canada.
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A low probability over-infusion may occur due to an open safety clamp fitment on the pumping segment whether opened intentionaly during expected clinical practice or as a result of inadvertent action.
Model Catalog: 2340-0500 (Lot serial: ALL LOTS); Model Catalog: 2330-0500 (Lot serial: ALL LOTS); Model Catalog: 2326-0500 (Lot serial: ALL LOTS); Model Catalog: 2320-0500 (Lot serial: ALL LOTS); Model Catalog: 2311-0500 (Lot serial: ALL LOTS); Model Catalog: 2306-0500 (Lot serial: ALL LOTS); Model Catalog: 2301-0500 (Lot serial: ALL LOTS); Model Catalog: 2280-0006 (Lot serial: ALL LOTS); Model Catalog: 2280-0000 (Lot serial: ALL LOTS); Model Catalog: 2277-0006 (Lot serial: ALL LOTS); Model Catalog: 2277-0000 (Lot serial: ALL LOTS); Model Catalog: 2264-0500 (Lot serial: ALL LOTS); Model Catalog: 2264-0006 (Lot serial: ALL LOTS); Model Catalog: 2260-0500 (Lot serial: ALL LOTS); Model Catalog: 2260-0006 (Lot serial: ALL LOTS); Model Catalog: 2255-0500 (Lot serial: ALL LOTS); Model Catalog: 2247-0600 (Lot serial: ALL LOTS); Model Catalog: 2241-0600 (Lot serial: ALL LOTS); Model Catalog: 9996-0000 (Lot serial: ALL LOTS); Model Catalog: 9987-0000 (Lot serial: ALL LOTS); Model Catalog: 9986-0500 (Lot serial: ALL L