FDA Device recall Z-2699-2017
Arrow Glide Thru Peel-Away Sheath/Dilator Introducer
- FDA Device
- Class II
- terminated
- Published 2017-07-19
On 2017-07-19 the FDA classified a Class II recall of Arrow Glide Thru Peel-Away Sheath/Dilator Introducer by Arrow International, citing 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 com….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2699-2017 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2017-06-12 |
| Published | 2017-07-19 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Arrow International |
| Distribution | AL, AZ, CA, GA, IN, MA, NJ, PA, SC, VA, WA |
Product
Arrow Glide Thru Peel-Away Sheath/Dilator Introducer
Reason
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.
Identifiers
| code_info | Device Listing # D184260 Material # PL-01055 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2699-2017%22
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