Z-0990-2014 Class II Terminated

Recalled by Perrigo Diabetes Care — Alpharetta, GA

Recall Details

Product Type
Devices
Report Date
February 26, 2014
Initiation Date
December 20, 2013
Termination Date
August 5, 2014
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
7924 units

Product Description

Orbit soft Infusion sets, 9 mm soft cannula, P10 (42") tubing; Single-Use Set Orbit Infusion Sets are sterile, non-pyrogenic, single-use devices intended to be used for subcutaneous delivery of medication , for example insulin, from an external infusion pump.

Reason for Recall

Perrigo was notified by our supplier, Ypsomed AG, that they are recalling these batches due to being manufactured with a non-conforming female luer-lock connector. The luer-lock connectors are incompatible with standard male luer-lock connectors for use in connection to compatible infusion pumps. Perrigo became was notified of a quality complaint related to this issue on November 20, 2013 from a

Distribution Pattern

Nationwide Distribution including GA & TX

Code Information

400064, 400069, 400070, & 400072 UPC: 7613117009502