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Manufacturers
Disetronic Medical Systems, Inc.
Manufacturer Address
Disetronic Medical Systems, Inc., 11800 Exit 5 Parkway, Suite 120, Fishers IN 46038
Source
USFDA
32 Events
Recall of Device Recall Dtron
Recall of Device Recall Disetronic
Recall of Device Recall Disetronic
Recall of Device Recall Disetronic
Recall of Device Recall Disetronic
Recall of Device Recall AccuChek
Recall of Device Recall AccuChek
Recall of Device Recall AccuChek
Recall of Device Recall AccuChek
Recall of Device Recall AccuChek
Recall of Device Recall AccuChek
Recall of Device Recall AccuChek
Recall of Device Recall AccuChek
Recall of Device Recall AccuChek
Recall of Device Recall AccuChek
Recall of Device Recall AccuChek
Recall of Device Recall AccuChek
Recall of Device Recall AccuChek
Recall of Device Recall AccuChek
Recall of Device Recall AccuChek
Recall of Device Recall AccuChek
Recall of Device Recall AccuChek
Recall of Device Recall AccuChek
Recall of Device Recall AccuChek
Recall of Device Recall AccuChek
Recall of Device Recall AccuChek
Recall of Device Recall AccuChek
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32 devices in the database
Device Recall Dtron
Model / Serial
Lots 06010107, 06030242, 06040085, 06050110 and 06060126.
Product Classification
General Hospital and Personal Use Devices
Device Class
2
Implanted device?
No
Distribution
Nationwide and Canada.
Product Description
Disetronic D-TRONplus Insulin Pump Battery Pack; Ref/Catalog no. 04697014001.
Device Recall Disetronic
Model / Serial
Lot 3H067UF.
Product Classification
General Hospital and Personal Use Devices
Device Class
2
Implanted device?
No
Distribution
Worldwide including USA, Argentina, Austria, Barbados, Belgium, Canada, Czech Republic, Denmark, Estonia, Finland, France, Germany, Greece, Honduras, Hungary, Italy, Mexico, Netherlands, New Zealand, Norway, Poland, Portugal, Singapore, Slovenia, Spain, Sweden, Switzerland and United Kingdom.
Product Description
Disetronic Ultraflex 10/110 infusion set; (Distributed outside of the US only).
Device Recall Disetronic
Model / Serial
Lot 3J012UF.
Product Classification
General Hospital and Personal Use Devices
Device Class
2
Implanted device?
No
Distribution
Worldwide including USA, Argentina, Austria, Barbados, Belgium, Canada, Czech Republic, Denmark, Estonia, Finland, France, Germany, Greece, Honduras, Hungary, Italy, Mexico, Netherlands, New Zealand, Norway, Poland, Portugal, Singapore, Slovenia, Spain, Sweden, Switzerland and United Kingdom.
Product Description
Disetronic Ultraflex 8/110 infusion set; (Distributed outside of the US only).
Device Recall Disetronic
Model / Serial
Lot 3G039UF.
Product Classification
General Hospital and Personal Use Devices
Device Class
2
Implanted device?
No
Distribution
Worldwide including USA, Argentina, Austria, Barbados, Belgium, Canada, Czech Republic, Denmark, Estonia, Finland, France, Germany, Greece, Honduras, Hungary, Italy, Mexico, Netherlands, New Zealand, Norway, Poland, Portugal, Singapore, Slovenia, Spain, Sweden, Switzerland and United Kingdom.
Product Description
Disetronic Ultraflex 8/80 infusion set; Catalog number 4489039001. (Distributed outside of the US only).
Device Recall Disetronic
Model / Serial
Lot 3H003UF.
Product Classification
General Hospital and Personal Use Devices
Device Class
2
Implanted device?
No
Distribution
Worldwide including USA, Argentina, Austria, Barbados, Belgium, Canada, Czech Republic, Denmark, Estonia, Finland, France, Germany, Greece, Honduras, Hungary, Italy, Mexico, Netherlands, New Zealand, Norway, Poland, Portugal, Singapore, Slovenia, Spain, Sweden, Switzerland and United Kingdom.
Product Description
Disetronic Ultraflex 8/60 infusion set; (Distributed outside of the US only).
27 more
One manufacturer with a similar name
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Disetronic Medical Systems, Inc.
Manufacturer Address
Disetronic Medical Systems, Inc., 11800 Exit 5 Pkwy Ste 120, Fishers IN 46037-7989
Source
USFDA
Language
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