Reported May 10, 2017 · Terminated
SurFlo IV Catheter
Terumo Medical Corporation
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: Terumo Medical Corporation · 950 Elkton Blvd · Elkton, MD · 21921-5322
Is this the product you have?
- SurFlo IV Catheter
- Lot codes and dates
- PRODUCT CODELOT NUMBER
3SR-OX2225CA3SR-OX2419CA3SR-OX2225CA3SR-OX2419CASR-TL2419M3SR-OX2419CA3SR-OX2225CASR-TL2225M3SR-OX2225CA3SR-OX2419CA3SR-OX2225CA3SR-OX2419CASR-TL2419M3SR-OX2225CA3SR-OX2225CA3SR-OX2225CA3SR-OX2225CASR-TL2225M3SR-OX2225CA3SR-OX2225CA3SR-OX2225CA3SR-OX2419CASR-TL2419M3SR-OX2419CA3SR-OX2419CA3SR-OX2419CA
RF2727RF2727RG0227RG0927RG0927RG1627RG2027RG2027RG2327RH0727RH1427RH1427RH1427RH2127RH2827RH3127RK0427RK0427RK1127RK1827RK2527RL0227RL0227RL0827RL1527RL2227
- PRODUCT CODE
- Amount recalled
- 2,478,200
This recall covers 2 products
The agency filed one notice per product. You are reading one of them; the other one is below.
Why it was recalled
According to the Terumo (TMC) this device is used to access the human peripheral vascular system for short term use (less than 30 days) for the purpose of infusing fluids into patients. A small percentage of the catheters in the affected lots may have damage to the ETFE catheter which may allow the catheter to break during withdrawal.
This product could cause temporary or reversible health problems — stop using it.
Want the full recall guide?
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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