RELIEVA FLEX Sinus Guide Catheter F-70 — Class III medical device recall Z-1740-2015
Terminated recall by Acclarent, Inc., reported 2015-06-17, distributed in TX. Acclarent determined that one single RELIEVA FLEX Sinus Guide Catheter was distributed past it's expiry date.
| Recall number | Z-1740-2015 |
|---|---|
| Product type | Medical device |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Acclarent, Inc., Menlo Park, CA, United States |
| Recall initiated | 2015-04-28 |
| Classified | 2015-06-09 |
| Reported by FDA | 2015-06-17 |
| Terminated | 2015-06-10 |
| Distributed | TX |
| Quantity | 986 |
| Lot numbers | 120709I-CM |
| Model numbers | GC070RF |
| Expiration dates | 2014-07-31 |
Product
RELIEVA FLEX Sinus Guide Catheter F-70. Catalog number GC070RF. Product Usage - Sinus Catheter - Intended to provide a means to access the sinus space for diagnostic and therapeutic procedures. .
Reason for recall
Acclarent determined that one single RELIEVA FLEX Sinus Guide Catheter was distributed past it's expiry 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-1740-2015. 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.