FDA Device recall Z-0558-2014
HT Connect Peripheral Guide Wire Part Number Description 1012587 018 HT CONNECT 145 CM 1012588 018 HT CONNECT 195 CM 1012589 018 HT CONNECT…
- FDA Device
- Class II
- terminated
- Published 2014-01-01
On 2014-01-01 the FDA classified a Class II recall of HT Connect Peripheral Guide Wire Part Number Description 1012587 018 HT CONNECT 145 CM 1012588 018 HT CONNECT 195 CM 1012589 018 HT CONNECT… by Abbott Vascular, citing abbott Vascular has initiated a recall of the HT Connect Peripheral Guide Wires due to a small number of devices exhibiting partial delamination of the PTFE coating.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0558-2014 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2013-11-25 |
| Published | 2014-01-01 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Abbott Vascular |
| Distribution | US |
Product
HT Connect Peripheral Guide Wire Part Number Description 1012587 018 HT CONNECT 145 CM 1012588 018 HT CONNECT 195 CM 1012589 018 HT CONNECT 300 CM 1012590 018 HT CONNECT FLEX 145 CM 1012591 018 HT CONNECT FLEX 195 CM 1012592 018 HT CONNECT FLEX 300 CM 1012593 018 HT CONNECT 250T 145 CM 1012594 018 HT CONNECT 250T 195 CM 1012595 018 HT CONNECT 250T 300 CM
Reason
Abbott Vascular has initiated a recall of the HT Connect Peripheral Guide Wires due to a small number of devices exhibiting partial delamination of the PTFE coating.
Identifiers
| code_info | Part Number Lot Number 1012587 10097079 1012587 10168703 1012587 10168705 1012587 10171679 1012587 10262897 10125…Part Number Lot Number 1012587 10097079 1012587 10168703 1012587 10168705 1012587 10171679 1012587 10262897 1012587 10281944 1012587 10303349 1012587 90021507 1012588 10087171 1012588 10087179 1012588 10108128 1012588 10108132 1012588 10137054 1012588 10137224 1012588 10155636 1012588 10155638 1012588 10156982 1012588 10171681 1012588 10181960 1012588 10186395 1012588 10187173 1012588 10201046 1012588 10201050 1012588 10202457 1012588 10213592 1012588 10213593 1012588 10220279 1012588 10220283 1012588 10220284 1012588 10226194 1012588 10226314 1012588 10226315 1012588 10226316 1012588 10226317 1012588 10226318 1012588 10244104 1012588 10303351 1012588 10303361 1012588 90020420 1012588 90020746 1012588 90021060 1012588 90021154 1012588 90021155 1012588 90021156 1012588 90021266 1012588 90021313 1012588 90021334 1012588 90021335 1012588 90021508 1012588 90021509 1012588 90021573 1012589 10087172 1012589 10087180 1012589 10087181 1012 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0558-2014%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.