Quick summary: Level 1 H-2 Pressure Chamber.
Level 1 H-2 Pressure Chamber
Recommended action: compare your product with the official notice and follow the instructions published by the official source.
Recall details
Quick summary: Level 1 H-2 Pressure Chamber.
Affected product details
Structured information extracted from the official recall notice. Confirm the identifiers and instructions in the original notice.
Affected products
Issue
Smiths Medical implemented a design change in 2016 to widen the hinge assembly on the Level 1 H-2 Pressure Chambers used with the Level 1 Fast Flow Fluid Warmers (Models H-1025 or H-1200) or added to the H-1000 model. Smiths Medical has become aware that Level 1 H-2 Pressure Chambers with the wider hinge assembly can potentially impact the amount of pressure exerted onto the IV fluid bag while contained within the pressure chamber. This may result in decreased flow rate, stopped flow or residual fluid left within the IV bag. Pressure chambers with the wide hinge assembly are more susceptible to this issue in the following scenarios: 1) kinked tubing on the disposable administration sets. 2) use of the lowest flow rate disposables (DI-50, D-70 or DI-70) when delivering viscous fluids such as chilled blood from 300 mL or smaller IV bags. Recall start date: July 28, 2022
What you should do
- Contact the manufacturer if you require additional information.
Additional official information
Contains information licensed under the Open Government Licence – Canada. SafetyPulse is independent of the Government of Canada.
Frequently asked questions
Answers based on the official recall notice.
Product images
Official product images from Health Canada.
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