FDA Enforcement Class II Terminated

Contact Detach, 8mm, 23", G29; Contact Detach 8 mm, 43", G29; Contact Detach, 6mm, 23" G29; Infusion Set, Contact Detach, 6mm x 23"; Infusion Set, Contact Detach, 6mm x 32"; Infusion Set, Contact Detach, 8mm x 23"; Infusion Set, Contact Detach, 8mm x 32" The products are used in combination with insulin infusion pumps for continuous subcutaneous infusion of insulin

Recall: Z-0356-2017 · Reported November 9, 2016

Enforcement

Recall Number
Z-0356-2017
Event ID
74242
Classification
Class II
Status
Terminated
Product Type
Devices
Firm
Unomedical As
Voluntary / Mandated
Voluntary: Firm initiated
Initial Notification
E-Mail
Report Date
November 9, 2016
Initiation Date
November 7, 2014
Classification Date
November 3, 2016
Termination Date
November 16, 2016
Address
Aholmvej 1 3 Osted, Roskilde, N/A, Denmark

Description

Contact Detach, 8mm, 23", G29; Contact Detach 8 mm, 43", G29; Contact Detach, 6mm, 23" G29; Infusion Set, Contact Detach, 6mm x 23"; Infusion Set, Contact Detach, 6mm x 32"; Infusion Set, Contact Detach, 8mm x 23"; Infusion Set, Contact Detach, 8mm x 32" The products are used in combination with insulin infusion pumps for continuous subcutaneous infusion of insulin

Reason

Tubing detachment

Code Info

5031810, 5034061, 5034232, 5035097, 5036348, 5038182, 5038183, 5038184, 5038185, 5038186, 5038187, 5038188, 5040990, 5040991, 5040992, 5041073, 5041074, 5045147, 5045148, 5047241, 5047242, 5047243, 5047245, 5048097, 5053689, 5054465, 5054466, 5054550, 5054553, 5054554, 5057103, 5057104, 5057105, 5057106, 5058633, 5058637, 5058731, 5058732, 5058733, 5058734, 5062769, 5062770, 5062780, 5062811, 5062812, 5062813, 5066512, 5066999, 5067219, 5067220, 5067221, 5067222, 5067223, 5067224, 5067225, 5067226, 5067574, 5068464, 5068465, 5071889, 5073670, 5073671, 5075505, 5075509, 5076078, 5054475, 5054476, 5054477, 5054478, 5063762, 5063763

Distribution

Worldwide Distribution - US including CA, IN, PA, and Internationally to Canada, Korea, and Japan.

Quantity

664,000 units