Perrigo Diabetes Care: Medical Device Recall in 2014 - (Recall #: Z-0990-2014)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2014.

Data Source: FDA.

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.

Product Classification:

Class II

Date Initiated: December 20, 2013

Date Posted: February 26, 2014

Recall Number: Z-0990-2014

Event ID: 67154

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

Status: Terminated

Product Quantity: 7924 units

Code Information:

400064, 400069, 400070, & 400072 UPC: 7613117009502

Distribution Pattern:

Nationwide Distribution including GA & TX

Voluntary or Mandated:

Voluntary: Firm initiated