FDA Device recall Z-1620-2020
Stryker Neurovascular, AXS Vecta 71 Aspiration Catheter, Ref
- FDA Device
- Class II
- terminated
- Published 2020-04-08
On 2020-04-08 the FDA classified a Class II recall of Stryker Neurovascular, AXS Vecta 71 Aspiration Catheter, Ref by Stryker Neurovascular, citing the firm has become aware of a potential problem that their Catheters may break/fracture and/or kink/bend if improperly removed from the packaging/dispenser hoop or during cathete….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1620-2020 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2019-04-10 |
| Published | 2020-04-08 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Stryker Neurovascular |
| Distribution | US |
Product
Stryker Neurovascular, AXS Vecta 71 Aspiration Catheter, Ref. Catalog No. INC-11129-115, Use By 2021-11-29, Rx Only, Sterile/EO, Manufactured For: Stryker Neurovascular 47900 Bayside Parkway, Fremont, CA 94538, UDI: (01)07613327459210(17)211129(10)00000-00 Stryker Neurovascular, AXS Vecta 71 Aspiration Catheter, Ref. Catalog No. INC-11129-125, Use By 2021-11-29, Rx Only, Sterile/EO, Manufactured For: Stryker Neurovascular 47900 Bayside Parkway, Fremont, CA 94538, UDI: (01)07613327459227(17)211129(10)00000-00 Stryker Neurovascular, AXS Vecta 71 Aspiration Catheter, Ref. Catalog No. INC-11129-132, Use By 2021-11-29, Rx Only, Sterile/EO, Manufactured For: Stryker Neurovascular 47900 Bayside Parkway, Fremont, CA 94538, UDI: (01)07613327459234(17)211129(10)00000-00 Product Usage: The AXS Vecta Aspiration System, including the AXS Vecta Aspiration Catheter, Aspiration Tubing Set, and VC-701 Cliq Aspirator Pump, is indicated in the revascularization of patients with acute ischemic stroke secondary to intracranial large vessel occlusive disease (within the internal carotid, middle cerebral-M1 and M2 segments, basilar, and vertebral arteries) within 8 hours of symptom onset. Patients who are ineligible for intravenous tissue plasminogen activator (IV t-PA) or who failed IV t-PA therapy are candidates for treatment.
Reason
The firm has become aware of a potential problem that their Catheters may break/fracture and/or kink/bend if improperly removed from the packaging/dispenser hoop or during catheter use.
Identifiers
| code_info | Catalog # INC-11129-115: (Lot #'s 13170-01,13301-01,13494-01,13543-01,13545-01) Catalog # INC-11129-125: (Lot #'s 1316…Catalog # INC-11129-115: (Lot #'s 13170-01,13301-01,13494-01,13543-01,13545-01) Catalog # INC-11129-125: (Lot #'s 13163-01,13302-01,13500-01,13530-01) Catalog # INC-11129-132: (Lot #'s 13131-01,13156-01,13158-01,13176-01,13200-01,13201-01,13208-01,13212-01,13213-01,13215-01,13222-01,13238-01,13260-01,13266-01,13289-01,13221-01,13410-01,13412-01,13520-01) |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1620-2020%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.