Get the free BD Recalls Alaris Infusion Pumps Due to Syringe ...

30 Tuas Avenue 2 Singapore 639461 Registration No. 201114149Nbd.comURGENT FIELD SAFETY NOTICE Product Name: Alaris GS, GH, CC, TIVA, PK, Enteral Syringe Pump Product codes with prefix (all variants):

How to fill out bd recalls alaris infusion

How to fill out bd recalls alaris infusion

1. Gather all necessary materials: BD recalls Alaris infusion pump, IV set, medication, and patient-specific information.
2. Confirm the recall information and check for any specific adjustments related to the infusion pump.
3. Set up the infusion pump according to the manufacturer's guidelines, ensuring all connections are secure.
4. Prepare the medication by following the prescribed dosage and any companion directives.
5. Load the medication into the IV set, ensuring that all air bubbles are expelled.
6. Program the infusion pump with the correct rate and volume as per the physician's orders.
7. Start the infusion and monitor the patient’s response, adjusting as necessary based on medical advice.
8. Document the infusion process and any patient observations for future reference.

Who needs bd recalls alaris infusion?

1. Patients requiring intravenous medication administration.
2. Healthcare providers involved in administering IV treatments.
3. Medical facilities implementing recalls and ensuring patient safety.

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What is bd recalls alaris infusion?

BD recalls Alaris infusion refers to a recall issued by Becton, Dickinson and Company (BD) for their Alaris infusion pumps due to specific safety concerns or manufacturing defects that could potentially harm patients.

Who is required to file bd recalls alaris infusion?

Healthcare providers, hospitals, and facilities using the Alaris infusion pumps are typically required to file reports regarding the recall with relevant regulatory bodies.

How to fill out bd recalls alaris infusion?

To fill out the BD recalls Alaris infusion report, users should follow the guidelines provided by BD, which usually includes providing details about the affected equipment, the nature of the recall, and any actions taken.

What is the purpose of bd recalls alaris infusion?

The purpose of BD recalls Alaris infusion is to ensure patient safety by addressing potential risks associated with the use of specific infusion pumps and to implement corrective actions.

What information must be reported on bd recalls alaris infusion?

Information that must be reported includes the model and serial numbers of the devices, the nature of the defect, any incidents or adverse events associated with the defect, and actions taken to rectify the issue.