Brand Name: Multirate Infusor Devices. Indicated for the intravenous administration of medications.
Reported: July 3, 2013 Initiated: June 7, 2013 #Z-1601-2013
Product Description
Brand Name: Multirate Infusor Devices. Indicated for the intravenous administration of medications.
Reason for Recall
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.
Details
- Recalling Firm
- Baxter Healthcare Corp.
- Units Affected
- 3,255,096 total
- Distribution
- Distributed Nationwide and in Puerto Rico.
- Location
- Round Lake, IL
Frequently Asked Questions
What product was recalled? ▼
Brand Name: Multirate Infusor Devices. Indicated for the intravenous administration of medications.. Recalled by Baxter Healthcare Corp.. Units affected: 3,255,096 total.
Why was this product recalled? ▼
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.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on July 3, 2013. Severity: Moderate. Recall number: Z-1601-2013.
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