Medical DeviceNov 9, 2016
Unomedical As Comfort 5+5 Pack w/110cm Tube & 17mm Cann recall — FDA Z-0358-2017
Tubing detachment
Class IIFDA: TerminatedUnomedical As
Recall history in this database
Classification mix: Class II: 7.
Medical DeviceNov 9, 2016
Unomedical As AC TenderLink 13/30 10 pcs recall — FDA Z-0357-2017
Tubing detachment
Class IIFDA: TerminatedUnomedical As
Medical DeviceNov 9, 2016
Unomedical As Contact Detach, 8mm, 23", G29 recall — FDA Z-0356-2017
Tubing detachment
Class IIFDA: TerminatedUnomedical As
Medical DeviceNov 9, 2016
Unomedical As SureT G29 6mm, 18", Paradigm recall — FDA Z-0360-2017
Tubing detachment
Class IIFDA: TerminatedUnomedical As
Medical DeviceNov 9, 2016
Unomedical As Silhouette Paradigm 13mm, 18" recall — FDA Z-0359-2017
Tubing detachment
Class IIFDA: TerminatedUnomedical As
Medical DeviceNov 9, 2016
Unomedical As Infusion Set, Comfort, 23" Hosp 10 recall — FDA Z-0355-2017
Tubing detachment
Class IIFDA: TerminatedUnomedical As
Medical DeviceJul 1, 2015
Unomedical As Sure T, contact, contact detach, neria, neria detach, neria multi and thalaset recall — FDA Z-1821-2015
Unomedical has found that in rare cases the steel needle can break during use, interrupting the delivery of medication including insulin.
Class IIFDA: TerminatedUnomedical As
Understanding this recall history
This page summarizes recall records in which the official source identifies Unomedical As as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.