Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field., part of PerrigoLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list Perrigo Diabetes Care with 1 device recall. The most recent is a device recall dated Dec 20, 2013: Orbit soft Infusion sets, 9 mm soft cannula, P10 (42") tubing; Single-Use Set Orbit Inf….
| Date | Record | Source |
|---|---|---|
| Dec 20, 2013 | Orbit soft Infusion sets, 9 mm soft cannula, P10 (42") tubing; Single-Use Set Orbit Infusion Sets are sterile, non-pyrogenic, single-use deClass II · Perrigo was notified by our supplier, Ypsomed AG, that they are recalling these batches due to being manufactured with a | Device recalls |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
