[Recalled] Brand Name: Intermate Infusion Pump. Indicated for the intravenous administration of medications. — Baxter Healthcare Corporation (Baxter) is issuing an Urgent Product Recall for… | FDA 2013-06-07
A safety authority has issued a recall or warning for this item. The confirmed facts from the source notice are laid out below.
Recall details
| Product | Brand Name: Intermate Infusion Pump. Indicated for the intravenous administration of medications. |
|---|---|
| Brand / manufacturer | Baxter Healthcare Corp. |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-1604-2013 |
| Country of notice | United States |
| Risk level | Class II |
| Hazard type | recall |
| Notice date | 07 June 2013 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: Baxter Healthcare Corporation (Baxter) is issuing an Urgent Product Recall for the products listed above due to an increase in rupture complaints. Baxter has implemented product and process improvements which have substantially improved product quality. Complaint rates for ruptures have since decreased. Baxter wants to ensure that no affected product remains in the field.
This Class II recall concerns device products distributed in United States and was recorded by FDA_DEVICE. Recalls in this category are published so that owners, retailers, and importers can identify affected units and act quickly.
What to do if you own this product
Check whether your unit is affected and follow the authority's guidance before further use.
Read the full official notice →
Related recalls from Baxter Healthcare Corp.
This page indexes a public government recall notice for reference. We do not sell or verify this product; always confirm the current status on the authority's official site.
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