Data Foundry

Medical device recalls 2014

HT Connect Peripheral Guide Wire Part Number Description 1012587 018… — Class II medical device recall Z-0558-2014

Terminated recall by Abbott Vascular, Inc., reported 2014-01-01, distributed nationwide. Abbott Vascular has initiated a recall of the HT Connect Peripheral Guide Wires due to a small number of devic

Recall numberZ-0558-2014
Product typeMedical device
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmAbbott Vascular, Inc., Temecula, CA, United States
Recall initiated2013-11-25
Classified2013-12-20
Reported by FDA2014-01-01
Terminated2014-07-14
DistributedNationwide (US)
Countries outside the USAE, AT, AU, BE, BG, BH, BR, CA, CH, CN, CZ, DE, DK, EE, ES, FI, FR, GB, GR, GY, HK, ID, IE, IQ, IR, IT, KR, LT, LU, LV, MY, NL, NO, NZ, PL, PT, SA, SE, SG, SI, SK, TH, TR, TW, ZA
Lot numbers10087171, 10087172, 10087174, 10087175, 10087177, 10087178, 10087179, 10087180, 10087181, 10087182, 10087183, 10087184, 10087185, 10087186, 10097079, 10101124, 10105164, 10105191, 10108128, 10108129, 10108132, 10108133, 10108328, 10111355, 10111356, 10111357, 10118216, 10118217, 10118218, 10118330, 10122329, 10122330, 10122343, 10122344, 1012587, 1012588, 1012589, 1012590, 1012591, 1012592 and 233 more
Model numbers10087171, 10087172, 10087174, 10087175, 10087177, 10087178, 10087179, 10087180, 10087181, 10087182, 10087183, 10087184, 10087185, 10087186, 10097079, 10101124, 10105164, 10105191, 10108128, 10108129, 10108132, 10108133, 10108328, 10111355, 10111356 and 248 more

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 for recall

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.

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0558-2014. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.