FDA Device recall Z-2120-2017
StatLock¿ IV Premium Catheter Stabilization Device, product code IV0570. sterile
- FDA Device
- Class II
- terminated
- Published 2017-05-31
On 2017-05-31 the FDA classified a Class II recall of StatLock¿ IV Premium Catheter Stabilization Device, product code IV0570. sterile by Bard Access Systems, citing statLockTM IV Premium Catheter Stabilization Device may contain an incorrectly sized retainer clip.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2120-2017 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2017-04-25 |
| Published | 2017-05-31 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Bard Access Systems |
| Distribution | US |
Product
StatLock¿ IV Premium Catheter Stabilization Device, product code IV0570. sterile. Packaging: packaged as single units in tyvek to film pouches, the product is distributed in cartons containing 25 devices and cases containing 250 devices.
Reason
StatLockTM IV Premium Catheter Stabilization Device may contain an incorrectly sized retainer clip.
Identifiers
| code_info | Lot Number JUAQF675, Exp 2/28/2019 |
|---|
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-2120-2017%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.