Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Orbit soft Infusion sets Recalled by Perrigo Diabetes Care Due to Perrigo was notified by our supplier, Ypsomed AG,...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Perrigo Diabetes Care directly.
Affected Products
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.
Quantity: 7924 units
Why Was This Recalled?
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
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Perrigo Diabetes Care
Perrigo Diabetes Care has 1 total recall tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report