Arrow Glide Thru Peel-Away Sheath/Dilator Introducer — Class II medical device recall Z-2699-2017
Terminated recall by Arrow International Inc, reported 2017-07-19, distributed in AL, AZ, CA, GA, IN, MA, NJ, PA…. Arrow is recalling additional lots that were identified as part of an active recall. Arrow is recalling the af
| Recall number | Z-2699-2017 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Arrow International Inc, Reading, PA, United States |
| Recall initiated | 2017-06-12 |
| Classified | 2017-07-07 |
| Reported by FDA | 2017-07-19 |
| Terminated | 2018-09-06 |
| Distributed | AL, AZ, CA, GA, IN, MA, NJ, PA, SC, VA, WA |
| Reason classes | device malfunction |
Product
Arrow Glide Thru Peel-Away Sheath/Dilator Introducer
Reason for recall
Arrow is recalling additional lots that were identified as part of an active recall. Arrow is recalling the affected product due to the possibility that the catheter peel-away component hub tabs may prematurely detach when the practitioner begins to peel apart the sheath body from the catheter.
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-2699-2017. 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.