58 results
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12ms
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Sources: EU EUDAMED, US FDA
Filters
Status: Terminated
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ExactaMix EVA Container, 250mL, REF: 737, Sterile R, Baxa Corporation, Englewood, CO 80112. A plastic container used to hold large-volume sterile solutions to be administered to a patient through an intravascular administration set
FDA Recall
Terminated
·Baxa Corporation·Product code LHI·March 8, 2011
ExactaMix EVA Container, 1000mL, REF: 739, Sterile R, Baxa Corporation, Englewood, CO 80112. A plastic container used to hold large-volume sterile solutions to be administered to a patient through an intravascular administration set
FDA Recall
Terminated
·Baxa Corporation·Product code LHI·March 8, 2011
ExactaMix EVA Container, Calibration Bag, REF: 735, Sterile R, Baxa Corporation, Englewood, CO 80112. A plastic container used to hold large-volume sterile solutions to be administered to a patient through an intravascular administration set
FDA Recall
Terminated
·Baxa Corporation·Product code LHI·March 8, 2011
ExactaMix EVA Container, 2000mL, REF: 740, Sterile R, Baxa Corporation, Englewood, CO 80112. A plastic container used to hold large-volume sterile solutions to be administered to a patient through an intravascular administration set
FDA Recall
Terminated
·Baxa Corporation·Product code LHI·March 8, 2011
ExactaMix EVA Container, 500mL, REF: 738, Sterile R, Baxa Corporation, Englewood, CO 80112. A plastic container used to hold large-volume sterile solutions to be administered to a patient through an intravascular administration set
FDA Recall
Terminated
·Baxa Corporation·Product code LHI·March 8, 2011
ExactaMix EVA Container, 3000mL, REF: 741, Sterile R, Baxa Corporation, Englewood, CO 80112. A plastic container used to hold large-volume sterile solutions to be administered to a patient through an intravascular administration set
FDA Recall
Terminated
·Baxa Corporation·Product code LHI·March 8, 2011
REFRESH CONTACTS Contact Lens Comfort Drops 0.4 fl oz (12 mL) Sterile
FDA Recall
Terminated
·Allergan PLC·Product code LPN·December 29, 2020
Exacta Mix TPN (total parenteral nutrition) Bag, Model 740, 2000mL, Baxa Corporation
FDA Recall
Terminated
·Baxa Corporation·Product code KPE·November 12, 2009
Exacta Mix TPN (total parenteral nutrition) Bag, Model 738, 500mL, Baxa Corporation.
FDA Recall
Terminated
·Baxa Corporation·Product code KPE·November 12, 2009
Exacta Mix TPN (total parenteral nutrition) Bag, Model 739, 1000mL, Baxa Corporation
FDA Recall
Terminated
·Baxa Corporation·Product code KPE·November 12, 2009
Exacta-Mix 2400 Valve Assembly w/Calibration Bag, Sterile R, 250 mL, Order No. REF: 724, Baxa Corporation.
FDA Recall
Terminated
·Baxa Corporation·Product code KPE·May 26, 2010
Exacta-Mix EVA Container, Sterile R, 500 mL, Order No. REF: 138, Baxa Corporation.
FDA Recall
Terminated
·Baxa Corporation·Product code KPE·May 26, 2010
Exacta-Mix EVA Container, Sterile R, 3000 mL, Order No. REF: 141, Baxa Corporation.
FDA Recall
Terminated
·Baxa Corporation·Product code KPE·May 26, 2010
Exacta-Mix EVA Container, Sterile R, 250 mL, Order No. REF: 137, Baxa Corporation.
FDA Recall
Terminated
·Baxa Corporation·Product code KPE·May 26, 2010
Exacta-Mix EVA Container, Sterile R, 4000 mL, Order No. REF: 142, Baxa Corporation.
FDA Recall
Terminated
·Baxa Corporation·Product code KPE·May 26, 2010
Exacta-Mix EVA Container, Sterile R, 2000 mL, Order No. REF: 140, Baxa Corporation.
FDA Recall
Terminated
·Baxa Corporation·Product code KPE·May 26, 2010
Exacta-Mix EVA Container, Sterile R, 1000 mL, Order No. REF: 139, Baxa Corporation.
FDA Recall
Terminated
·Baxa Corporation·Product code KPE·May 26, 2010
Exacta-Mix EVA Container, Sterile R, 5000 mL, Order No. REF: 143, Baxa Corporation.
FDA Recall
Terminated
·Baxa Corporation·Product code KPE·May 26, 2010
Exacta-Mix Calibration Bag, Sterile R, non-pyrogenic fluid path, 250 mL Reorder No. H938 371 3, Manufactured for Baxa Corporation.
FDA Recall
Terminated
·Baxa Corporation·Product code KPE·May 26, 2010
Halobag EVA Dual-Chamber Bag, Sterile R, 3000 mL Total Volume W/500 mL upper chamber, Order No. REF: 341, Baxa Corporation.
FDA Recall
Terminated
·Baxa Corporation·Product code KPE·May 26, 2010