Reported Jul 3, 2013 · Terminated
Brand Name: Multirate Infusor Devices. Indicated for the intravenous administration of medications.
Baxter Healthcare Corp.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Baxter Healthcare Corp. · Route 120 And Wilson Rd · Round Lake, IL · 60073-9799
Is this the product you have?
- Brand NameMultirate Infusor Devices. Indicated for the intravenous administration of medications
- Lot codes and dates
- Product Codes
2C1154KP2C1155KP2C9960KP2C9961KP
- Lot Numbers
10F03010F06610H04310H10410K02710K09910M09010G02810J05910M01910M08910F05810G06910G04210J04810M026
- Expiration Date06/30/13
- Product Codes
- Amount recalled
- 3,255,096 total
This recall covers 11 products
The agency filed one notice per product. You are reading one of them; the other 10 are below.
Where it was sold
- Nationwide
- PR
Why it was 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.
This product could cause temporary or reversible health problems — stop using it.
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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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