Kii Shielded Bladed trocars — Class II medical device recall Z-2533-2017
Terminated recall by Applied Medical Resources Corp, reported 2017-06-21. Due to possibility of insufficient sterilization.
| Recall number | Z-2533-2017 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Applied Medical Resources Corp, Rancho Santa Margarita, CA, United States |
| Recall initiated | 2017-05-04 |
| Classified | 2017-06-13 |
| Reported by FDA | 2017-06-21 |
| Terminated | 2018-03-06 |
| Countries outside the US | AU, FI, FR, GB |
| Lot numbers | 1269692, 1269694, 1271037, 1275188, 1275207, 1279039, 1279542, 1282163, 1283226, 1283892, 1287785, 1288759, 1288910 |
Product
Kii Shielded Bladed trocars (CTB14), Kii Low profile trocars (CTB23), and Kii 5x55mm Optical Z-Thread Dual Pack (CTR14) trocars.
Reason for recall
Due to possibility of insufficient sterilization.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2533-2017. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.