58 results
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19ms
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Sources: EU EUDAMED, US FDA
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FDA Recall
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Churchill Medical Systems Winged Infusion Set, 22Ga, 1", Latex-Free Winged Infusion Set Product Code: MBS-2210 Huber type needle set used for the infusion of medical fluids into implantable ports.
FDA Recall
Terminated
·Churchill Medical Systems, Inc.·Product code FMI·April 16, 2012
19Ga x 1 Huber Needle Set. Product Code: MBS-1910.
FDA Recall
Terminated
·Vygon MFG, Inc., dba/ Churchill Medical Systems, Inc.·Product code FMI·July 24, 2017
Embrace2- Indicated for use as an adjunct to seizure monitoring of adults and children age 6 and up in home or healthcare facilities during periods of rest. Models: (1) Flamingo Pink EM2-FP-S; (2) Sky Blue EM2-SB-2; (3) Seoul Grey EM2-SG-S; (4) Boston Blue EM2-BB-S; (5) Milan Black EM2-MB-S
FDA Recall
Open, Classified
·EMPATICA SRL Via Enrico Stendhal·Product code POS·July 13, 2023
Kion Anesthesia Workstation Maquet Critical Care AB SE-171-95 Solna, Sweden
FDA Recall
Terminated
·MAQUET Inc.·Product code BSZ·July 10, 2007
Servo-Ventilator, SV300/300A, Part numbers 6070391 and 6424704. The Safety Alert action targets customers with Unit Serial numbers 24578 and lower. Manuf. Maquet Critial Care AB, SE-171 95 Solna, Sweden.
FDA Recall
Terminated
·Maquet Inc·Product code CBK·January 3, 2005
Theratron Elite 80 Cobalt Radiotherapy
FDA Recall
Terminated
·MDS Canada Inc. DBA MDS Nordion·Product code IWB·July 8, 2004
Theratron Phoenix Cobalt Radiotherapy
FDA Recall
Terminated
·MDS Canada Inc. DBA MDS Nordion·Product code IWB·July 8, 2004
Theratron 780E Cobalt Radiotherapy
FDA Recall
Terminated
·MDS Canada Inc. DBA MDS Nordion·Product code IWB·July 8, 2004
Theratron 780C Cobalt Radiotherapy
FDA Recall
Terminated
·MDS Canada Inc. DBA MDS Nordion·Product code IWB·July 8, 2004
Theratron Elite 100 Cobalt Radiotherapy
FDA Recall
Terminated
·MDS Canada Inc. DBA MDS Nordion·Product code IWB·July 8, 2004
Theratron 1000E Cobalt Radiotherapy
FDA Recall
Terminated
·MDS Canada Inc. DBA MDS Nordion·Product code IWB·July 8, 2004
Theratron 1000 Cobalt Radiotherapy
FDA Recall
Terminated
·MDS Canada Inc. DBA MDS Nordion·Product code IWB·July 8, 2004
Portex Adult Single Limb Anesthesia Breathing Circuit, single use, Part Numbers: 386000 and 384001. Manufactured for Sims Portex, Inc., Fort Meyers, FL, Made in Mexico.
FDA Recall
Terminated
·MMS Sales Corp·Product code CAI·February 21, 2005
Circuit-Unilimb, Adult, 1M (40''), Disposable, Clean Non-sterile, Adult Anesthesia Circuit, Part Numbers DYNJAAF4000, DYNJAAF6225, and DYNJAAF6261. Manufactured for Medline Industries, Inc., Mundelein, IL 60060, Made in Mexico.
FDA Recall
Terminated
·MMS Sales Corp·Product code CAI·February 21, 2005
Coaxial Rebreathing Circuit 1.5 M and 2 M, single use, Part nubers T61500 (1.5 M) and T18116 (2 M). Manufactured for GEO Logistics, Copenhagen, Denmark, Made in Mexico
FDA Recall
Terminated
·MMS Sales Corp·Product code CAI·February 21, 2005
Circuit-Nexus, Adult, single use, Part Numbers: N7A110CG06, N4A100CE06, C4N0121000, 60010-1B, and 40301-1-2730. Manufactured for MMS Sales Corporation, 218 Highline Road, Pharr, Texas 78577, Made in Mexico.
FDA Recall
Terminated
·MMS Sales Corp·Product code CAI·February 21, 2005
Circuit-Unilimb, Pediatric, 1M (40''), Disposable, Clean Non-Sterile, Pediatric Anesthesia Circuit, Part Number DYNJAPF4000. Manufactured for Medline Industries, Inc., Mundelein, IL 60060, Made in Mexico.
FDA Recall
Terminated
·MMS Sales Corp·Product code CAI·February 21, 2005
Meridian Nexus, single use. Part Numbers: C4N00D001, 15867, 15880, 15880-30, 12000-1, 40000-1, 40200-1, 40301-1, 40301-1ML, 40301-1-13, 40301-1-13MM, 40301-1-24, 40301-1-30, 40302-1C24, 60000-1, 60201-1, 60300-M, 60301-1, 60301-1-24, 60302-1HM30-70, 60301-13042M, 72300-1-4-30-70, 72301-1, 72000-50-7589, 60301-1304042, and 72000-75. Manufactured for MMS Sales Corporation, 218 Highline Road, Pharr, Texas 78577, Made in Mexico.
FDA Recall
Terminated
·MMS Sales Corp·Product code CAI·February 21, 2005
Meridian Nexus- Pediatric, single use Part Numbers 60211-1304042, 60111-1, 60111-1MN, 40111-13042, 15900, 40010-1, and 40111-1. Manufactured for MMS Sales Corporation, 218 Highline Road, Pharr, Texas 78577, Made in Mexico.
FDA Recall
Terminated
·MMS Sales Corp·Product code CAI·February 21, 2005
Circuit- Matching Kit, 40'' Adult, 3L LPF, single use, Part Numbers RP640F0D0 and RP660F0D0. Manufactured for Pall Life Sciences, Ann Arbor, Michigan. Made in Mexico.
FDA Recall
Terminated
·MMS Sales Corp·Product code CAI·February 21, 2005