Gyrus Acmi, Incorporated: Medical Device Recalls in 2015

Updated on March 25, 2026.

According to to data from the FDA, there were 2 medical device recalls made by Gyrus Acmi, Incorporated in 2015. See the details of the recalls below.

You can see similar recalls for other firms.

Data Source: FDA.

See this for other years:

Gyrus ACMI Diego Elite Tubeset, intended for cutting, coagulation, drilling, debriding, and removal of bone, and soft and hard tissue in general ENT, Sinus/Rhinology, Nasopharyngeal/Laryngology, and Head and Neck procedures. Catalog No. TS101DC, Lot numbers JC924165 and below; Rx Only, STERILE EO
Gyrus ACMI Diego Elite Tubeset; intended for cutting, coagulation, drilling, debriding, and removal of bone, and soft and hard tissue in general ENT, Sinus/Rhinology, Nasopharyngeal/Laryngology, and Head & Neck procedures. Catalog No. TS100S, Lot numbers JC929332 and below, Rx Only, STERILE EO