Reported Feb 21, 2018 · Terminated
Central Venous Tray Triple Lumen Polyurethane Catheter, Catalog Identifier: C-UTLMY-501J-CCT Product Usage: The central…
Cook Inc.
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: Cook Inc. · 750 N Daniels Way · Bloomington, IN · 47404-9120
Is this the product you have?
6 of 6 products
| # | Product as published |
|---|---|
| 1 | Continuous or intermittent drug infusions |
| 2 | Central venous blood pressure monitoring (CVP) |
| 3 | Acute hyperalimentation |
| 4 | Blood sampling |
| 5 | Delivery of whole blood or blood products |
| 6 | Simultaneous, separate infusion of drugs |
- Lot codes and dates
- Lot Number (Expiration date)5901462 (30-January-2018)
- Amount recalled
- 50
This recall covers 5 products
The agency filed one notice per product. You are reading one of them; the other 4 are below.
Where it was sold
Why it was recalled
Central venous catheters may not fit over guide wire potentially causing procedure delay.
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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