The Recall Desk
HighFDA (Devices)·Z-0521-2017·Announced 2016-11-23

ICU Medical Recalls SafeSet Reservoir Kits Due to Potential Leak

ICU Medical is recalling 10 units of SafeSet Reservoir and blood sampling kits containing Transpac IV transducers due to a potential for leak.

What this means for you

Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.

Our severity reasoning: The recall involves a medical device with a potential leak hazard where no injuries or illnesses have been reported, fitting the rubric for risk-of-harm products where injury has not yet been reported.

Plain-English summary

ICU Medical, Inc. is recalling 10 units of SafeSet Reservoir and blood sampling kits, Item No. 46097-30, which contain Transpac IV transducers. The product is identified by code 3256959 and was distributed nationwide.

The recall was initiated because the company identified a potential for leak with these specific kits. The SafeSet Reservoir system is a blood sampling system assembled directly to the patient monitoring line, used on patients where periodic blood sampling is required.

The source text does not specify instructions for consumers or healthcare providers regarding the disposal or return of the affected units.

The recalled product

Product
SAFESET" KIT W/03ML FLUSH DEVICE FOR HOLMES REG. M.C., Item No. 46097-30 The Transpac Disposable Straight Pressure Transducer (DSPT) is an extravascular pressure transducer that interfaces between a catheter and pressure monitor by converting changes in pressure into electrical
Manufacturer
ICU Medical, Inc.
Hazard
Affected units
10

Is your product affected?

Check your packaging against the codes below. If any of them match, the product is part of this recall.

Lot numbers (1)

  • 3256959

Distribution

Distributed nationwide across the United States.

Part of a larger recall action

This product is one of 162 recalled by ICU Medical, Inc. under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.

See all 162 products in this recall →