COVIDIEN Emprint Ablation Catheter with Thermosphere Technology — Class II medical device recall Z-0955-2023
Ongoing recall by Covidien, LLC, reported 2023-01-18. The product is labeled with the incorrect expiration date.
| Recall number | Z-0955-2023 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Covidien, LLC, Minneapolis, MN, United States |
| Recall initiated | 2022-11-23 |
| Classified | 2023-01-12 |
| Reported by FDA | 2023-01-18 |
| Countries outside the US | HK |
| Quantity | 21 units |
| Reason classes | labeling |
| UPC / GTIN / UDI-DI | 10884521825765 |
| Lot numbers | 520200 |
| Model numbers | CA108L1 |
Product
COVIDIEN Emprint Ablation Catheter with Thermosphere Technology, Bronchoscopic Ablation, REF CA108L1
Reason for recall
The product is labeled with the incorrect expiration date.
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-0955-2023. 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.