46 results
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47ms
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Sources: EU EUDAMED, US FDA
Filters
FDA Recall
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Inspiration Ventilator System, i Series and LS 12.1 LCD. The Inspiration 7i / 5i Ventilator System is to be used by healthcare professionals in hospitals or healthcare facilities and intra-hospital transport.
FDA Recall
Terminated
·Event Medical LTD·Product code CBK·October 13, 2015
Asahi KASEI, REXEED(TM)- 18 SX, HEMODIALYZER dialysis filter
FDA Recall
Terminated
·Asahi Kasei Medical Co., Ltd., Okatomi Plant 4960 5 Chome Nakagawara Cho Nobeoka-shi Japan·Product code KDI·September 21, 2012
Asahi KASEI, REXEED(TM)- 13 LX, HEMODIALYZER dialysis filter
FDA Recall
Terminated
·Asahi Kasei Medical Co., Ltd., Okatomi Plant 4960 5 Chome Nakagawara Cho Nobeoka-shi Japan·Product code KDI·September 21, 2012
Asahi KASEI, REXEED(TM)- 15 LX, HEMODIALYZER dialysis filter
FDA Recall
Terminated
·Asahi Kasei Medical Co., Ltd., Okatomi Plant 4960 5 Chome Nakagawara Cho Nobeoka-shi Japan·Product code KDI·September 21, 2012
Asahi KASEI, REXEED(TM)- 25 SX, HEMODIALYZER dialysis filter
FDA Recall
Terminated
·Asahi Kasei Medical Co., Ltd., Okatomi Plant 4960 5 Chome Nakagawara Cho Nobeoka-shi Japan·Product code KDI·September 21, 2012
Asahi KASEI, REXEED(TM)- 18 LX, HEMODIALYZER dialysis filter
FDA Recall
Terminated
·Asahi Kasei Medical Co., Ltd., Okatomi Plant 4960 5 Chome Nakagawara Cho Nobeoka-shi Japan·Product code KDI·September 21, 2012
Asahi KASEI, REXEED(TM)- 21 SX, HEMODIALYZER dialysis filter
FDA Recall
Terminated
·Asahi Kasei Medical Co., Ltd., Okatomi Plant 4960 5 Chome Nakagawara Cho Nobeoka-shi Japan·Product code KDI·September 21, 2012
Asahi KASEI, REXEED(TM)- 15 SX, HEMODIALYZER dialysis filter
FDA Recall
Terminated
·Asahi Kasei Medical Co., Ltd., Okatomi Plant 4960 5 Chome Nakagawara Cho Nobeoka-shi Japan·Product code KDI·September 21, 2012
Spacelabs Healthcare CardioCall ECG Event Recorder, Models VS20, VS20x4, ST80, ST80x4, PCBAs PN # 670-1670-00 Product Usage: The CardioCall event recorder is worn by the patient to record a short period of electrocardiogram which can be sent to his physician.
FDA Recall
Terminated
·Spacelabs Healthcare Inc·Product code DXH·September 3, 2015
Description/REF: PICC ACCESS TRAY/ASK-04001-CG1
FDA Recall
Open, Classified
·ARROW INTERNATIONAL, LLC·Product code LJT·April 21, 2026
Description/REF: BIOPSY SYSTEM COMPREHENSIVE KIT/ASK-09458-AH, ASK-09458-COC, ASK-09458-EUH, ASK-09458-SD, ASK-09458-VU
FDA Recall
Open, Classified
·ARROW INTERNATIONAL, LLC·Product code POZ·April 21, 2026
Description/REF: PACING/PSI KIT: 5 FR 2L/ASK-07155-MGU
FDA Recall
Open, Classified
·ARROW INTERNATIONAL, LLC·Product code LDF·April 21, 2026
PARACENTESIS KIT, REF: AK-00376, ASK-00376-VCU
FDA Recall
Open, Classified
·ARROW INTERNATIONAL, LLC·Product code PYC·April 21, 2026
Description/REF: PERITONEAL LAVAGE CATH KIT:8FR/AK-09000
FDA Recall
Open, Classified
·ARROW INTERNATIONAL, LLC·Product code GBW·April 21, 2026
Description/REF: HEMODIALYSIS KIT: 2-LUMEN 12 FR X 16 CM/AK-12122-F
FDA Recall
Open, Classified
·ARROW INTERNATIONAL, LLC·Product code LFJ·April 21, 2026
Description/REF: PI MIDLINE 2L: 5FR X 20CM/CDC-32052-MPKC
FDA Recall
Open, Classified
·ARROW INTERNATIONAL, LLC·Product code PND·April 21, 2026
Description/REF: ACCESS TRAY/ASK-04001-MC3
FDA Recall
Open, Classified
·ARROW INTERNATIONAL, LLC·Product code PXB·April 21, 2026
Description/REF: PARACENTESIS KIT/ASK-00376-JHH
FDA Recall
Open, Classified
·ARROW INTERNATIONAL, LLC·Product code KDD·April 21, 2026
Description/REF: HEMODIALYSIS KIT: 2L 14 FR X 20 CM AGB CDC-25142-X1A
FDA Recall
Open, Classified
·ARROW INTERNATIONAL, LLC·Product code PPO·April 21, 2026
Description/REF: PACING PSI KIT: 6 FR/AI-06210-KS, PACING PSI KIT: 5 FR 2-L/AI-07155-KS, PACING PSI KIT: 5 FR 2L/ASK-07155-UPM
FDA Recall
Open, Classified
·ARROW INTERNATIONAL, LLC·Product code OES·April 21, 2026