105 results
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18ms
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Sources: EU EUDAMED, US FDA
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FDA Recall
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Terumo Cardiovascular Custom Cardiovascular Procedure Kits containing an Overpressure Safety Valve, LN130B, in the Arterial Recirculation Line
FDA Recall
Terminated
·Terumo Cardiovascular Systems Corporation·Product code MNJ·June 4, 2013
Reusable distal attachments Models: MH-462, MH-463, MH-464, MH-465, MH-466, MH-483, MH-587, MH-588(US), MH-589, MH-590, MH-591, MH-592, MH-593, MH-594, MH-595, MH-596, MH-597, MH-598, MAJ-289, MAJ-290, MAJ-291, MAJ-292, MAJ-293, MAJ-294, MAJ-295, MAJ-296, MAJ-297, MAJ-663, MAJ-664, MAJ-665, MAJ-666
FDA Recall
Open, Classified
·Aomori Olympus Co., Ltd. 2 Chome 248-1 Okkonoki Kuroishi Japan·Product code FDS·July 27, 2023
Bedside PICC CDS Convenience Kit
FDA Recall
Terminated
·Medline Industries Inc·Product code OEZ·October 27, 2021
Neuro Convenience Kit
FDA Recall
Terminated
·Medline Industries Inc·Product code OJG·October 27, 2021
Major Vascular CDS Convenience Kit
FDA Recall
Terminated
·Medline Industries Inc·Product code LRO·October 27, 2021
Venous Access Pack-LF Convenience Kit
FDA Recall
Terminated
·Medline Industries Inc·Product code OFF·October 27, 2021
EVLP Convenience Pack/Kit
FDA Recall
Terminated
·Medline Industries Inc·Product code LRO·October 27, 2021
Olympus Endoscope Suction Valve - MAJ-1443. Model Number: MAJ-1443.
FDA Recall
Open, Classified
·Olympus Corporation of the Americas·Product code ODC·February 12, 2026
Olympus Endoscope Air/Water Valve - MAJ-1444. Model Number: MAJ-1444.
FDA Recall
Open, Classified
·Olympus Corporation of the Americas·Product code ODC·February 12, 2026
Water Filter MAJ-2318. This MAJ-2318 water filter has been designed to be used with Olympus endoscope reprocessor for prevent contamination of the rinse water. The MAJ-2318 water filter is compatible with OER-ELITE and OER-MINI.
FDA Recall
Open, Classified
·Olympus Corporation of the Americas·Product code FEB·January 16, 2024
MAJ-247 SINGLE USE 30MM REPLACEMENT BASKET, model no. MAJ-247 - Product Usage: REPLACEMENT BASKET for BML-3Q Mechanical Lithotripter.
FDA Recall
Terminated
·Aomori Olympus Co., Ltd. 2 Chome 248-1 Okkonoki Kuroishi Japan·Product code LQC·January 4, 2021
MAJ-244 SINGLE USE 30MM REPLACEMENT BASKET, model no. MAJ-244 - Product Usage: REPLACEMENT BASKET for BML-3Q Mechanical Lithotripter.
FDA Recall
Terminated
·Aomori Olympus Co., Ltd. 2 Chome 248-1 Okkonoki Kuroishi Japan·Product code LQC·January 4, 2021
Outlook Pump Set w/150 ml Burette w/15um Filter & Inj Site, Check Valve, 2 Inj Sites, 120 in V7421M
FDA Recall
Terminated
·B. Braun Medical, Inc.·Product code FPA·November 24, 2009
Outlook Pump Set w/150 ml Burette w/15um Filter & Safeline Inj Site, Check Valve, 2 Safeline Inj Sites, 120 in NF3115M
FDA Recall
Terminated
·B. Braun Medical, Inc.·Product code FPA·November 24, 2009
Outlook Pump Set w/150 ml Burette w/Ultrasite Inj Site & 15um Filter, 2 Ultrasite Inj Sites, Check Valve 120 in US3116M
FDA Recall
Terminated
·B. Braun Medical, Inc.·Product code FPA·November 24, 2009
Outlook Pump Set w/150 ml Burette w/15um Filter & Ultrasite Inj Site, 2 Ultrasite Inj Sites, Check Valve 120 in US3116M
FDA Recall
Terminated
·B. Braun Medical, Inc.·Product code FPA·November 24, 2009
Outlook Pump Set w/150 ml Burette w/Ultrasite Inj Site & 15um Filter, 2 Safesite Inj Sites, Check Valve 120 in SS3115M
FDA Recall
Terminated
·B. Braun Medical, Inc.·Product code FPA·November 24, 2009
Outlook Pump Set w/150 ml Burette w/15um Filter & Ultrasite Inj Site, B/C Valve, 2 Ultrasite Inj Sites, 120 in US3121M
FDA Recall
Terminated
·B. Braun Medical, Inc.·Product code FPA·November 24, 2009
Burette Set w/150 ml Burette w/15 um filter & Ultrasite inj site, Ultrasite inj site, 88 in US1540. Item/Catalog number 375137. The product is shipped 20 units per carton. The product is for use after activation of shutoff valve (re-floating of disk)
FDA Recall
Terminated
·B. Braun Medical, Inc.·Product code FPA·June 30, 2008
Burette Set w/150 ml burette w/15 um filter & inj site, inj site, with automatic shutoff 87 in. Item/Catalog number 375113. The product is shipped 20 units per carton. The product is for use after activation of shutoff valve (re-floating of disk)
FDA Recall
Terminated
·B. Braun Medical, Inc.·Product code FPA·June 30, 2008