Recall archive
54 recalls · page 3 of 3
Reported Oct 1, 2014
STAT 2 Flow Controller; 80" (203 cm) Appx 14.8 mL, 20 Drop Primary Set w/2 Clave, STAT 2 Flow Controller, Rotating…
High riskUsing this product could cause serious injury, illness or death — stop using it now.ICU Medical, Inc.
Matched: Brand · Reason for recall — ICU is recalling the ConMed Stat 2 flow controller because it may deliver a significantly higher flow rate than was intended.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 27, 2014
CAP Change Kit w/MicroClave Clear, Item No. B78109 BD prefilled syringes are co-packaged into a kit with ICU devices…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ICU Medical, Inc.
Matched: Brand · Product · Product details · Reason for recall — ICU Medical is recalling the BD PosiFlush Sterile Field Saline Flush Syringe because some unit packages may exhibit open seals which impacts package…
2 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 13, 2014
Transpac IV Trifurcated Monitoring Kit w/84" Safeset Reservoir, 03 ml Squeeze Flush and 2 Clave Sampling Ports, Item…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ICU Medical, Inc.
Matched: Brand · Reason for recall — ICU has become aware of an issue with a component where the connection on an arterial monitoring kit may crack and cause a fluid leak.
8 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 15, 2014
NanoClave Connector, Part No. A1000, Item No. 011-A1000, 061-A1000, A1000, K7083-001, Z3769 The ICU Needleless…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ICU Medical, Inc.
Matched: Brand · Product · Product details · Reason for recall — ICU Medical is recalling certain lots of the NanoClave Needlefree Connector product line because of a small percentage of devices that may leak.
49 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 17, 2012
3 PORT "OFF" MANIFOLD w/WASTE BAG, SYRINGE and DyePod¿, Part Number (Item #) AG8049-NS, Lot # 2528655. K914299. Waste…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ICU Medical, Inc.
Matched: Brand · Reason for recall — ICU Medical, Inc. has identified a potential comingling of components where a 60 drop micro drip chamber may have been included on a 20 drop macro…
FDA (openFDA device enforcement)
Reported Aug 8, 2012
High Pressure Stopcock (3-Way, Luer Lock, Off). Product Usage: For IV.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ICU Medical, Inc.
Matched: Brand — The firm initiated the recall due to a molding defect in a high pressure stopcock where a small percentage of the side ports could become totally…
3 more products in this recall
FDA (openFDA device enforcement)
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