Dministration Set With 1, 2, 3 Connectors, Standard Bore Extension Set With Bonded Maxplus Connector, Minibore Extension Set, Maxplus Positive Pressure Needleless IV Connector (2019-04-23)
Recall Summary Several intravenous (IV) administration and connector products manufactured by Baxter are being recalled across Canada due to manufacturing defects in the devices. The recall affects Administration Sets with connectors, Extension Sets, and MaxPlus Positive Pressure Needleless IV Connectors distributed nationwide. These products are used in hospitals and healthcare settings to deliver medications and fluids to patients.
- Reason
- Medical devices
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2019-05-10
- Status
- Ongoing
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/ba4ce86f-af7f-4a5a-9627-07efc1231904