Alaris Pump Module Model 8100 and Certain Alaris Pump Infusion Sets. Weakening of the plastic can lead to damage or separation of the bezel posts which can cause issues with infusion, or unintended delivery of medication when pump module is not in running status.
Compare the exact product and every lot, model, serial range or date listed in the official notice. A similar name alone does not establish that your product is included.
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Manufacturer & model: Device name, model or catalog number from its label or packaging. Serial, lot or UDI: The identifiers specified in the notice; retain packaging where possible. Version & care records: Software version when relevant, or an implant card and clinician’s records.
Read the medical devices identification guideWhy this notice was issued
Weakening of the plastic can lead to damage or separation of the bezel posts which can cause issues with infusion, or unintended delivery of medication when pump module is not in running status
Official action
Open the official FDA notice to confirm whether your product is included and read the current instructions from the agency and manufacturer.
Follow the specific instructions and use the contact details in the announcement if you need help confirming a match or arranging the remedy.
Read the full official instructionsProduct & source details
- Product
- Alaris Pump Module Model 8100 and Certain Alaris Pump Infusion Sets
- Brand or manufacturer
- Alaris
- Source
- FDA
- Notice type
- Recall
- Category
- Medical devices