FDA Device recall Z-1139-2020
NC TREK Coronary Dilatation Catheter, REF 1012455-120 Rx Only,NC TREK RX 5.00 X 20MM BDC The NC TREK RX Coronary Dilatation Catheter is ind…
- FDA Device
- Class I
- terminated
- Published 2020-02-26
On 2020-02-26 the FDA classified a Class I recall of NC TREK Coronary Dilatation Catheter, REF 1012455-120 Rx Only,NC TREK RX 5.00 X 20MM BDC The NC TREK RX Coronary Dilatation Catheter is ind… by Abbott Vascular, citing coronary Dilatation Catheters may exhibit difficulty or inability to deflate the balloon.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1139-2020 |
| Classification | Class I |
| Status | terminated |
| Initiated | 2020-01-29 |
| Published | 2020-02-26 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Abbott Vascular |
| Distribution | n/a |
Product
NC TREK Coronary Dilatation Catheter, REF 1012455-120 Rx Only,NC TREK RX 5.00 X 20MM BDC The NC TREK RX Coronary Dilatation Catheter is indicated for: a) balloon dilatation of the stenotic portion of a coronary artery or bypass graft stenosis, for the purpose of improving myocardial perfusion b) balloon dilatation of a coronary artery occlusion, for the purpose of restoring coronary flow in patients with ST-segment elevation myocardial infarction c) balloon dilatation of a stent after implantation (balloon models 2.00 mm 5.00 mm only)
Reason
Coronary Dilatation Catheters may exhibit difficulty or inability to deflate the balloon.
Identifiers
| code_info | Device Identifier/GTIN: 08717648152160 Part Number: 1012455-20 Lot Numbers:91010G1 91026G1 |
|---|
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-1139-2020%22
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