Slip-Cath Beacon Tip Catheter — Class I medical device recall Z-2319-2015

Terminated recall by Cook Inc., reported 2015-08-12, distributed nationwide. Reports of catheter tip splits and or separation. Loss of device function, medical intervention to retrieve se

Recall number	`Z-2319-2015`
Product type	Medical device
Classification	Class I
Status	Terminated
Voluntary or mandated	Voluntary
Recalling firm	Cook Inc., Bloomington, IN, United States
Recall initiated	2015-07-02
Classified	2015-08-05
Reported by FDA	2015-08-12
Terminated	2017-09-02
Distributed	Nationwide (US)
Countries outside the US	AE, AT, AU, BD, BE, BG, BH, BR, BS, CA, CH, CL, CN, CO, CR, CY, CZ, DE, DK, DO, DZ, EG, ES, FI, FR, GB, GH, GR, HK, HU, ID, IE, IL, IN, IQ, IS, IT, JO, JP, KR, KW, LB, LK, LT, LV, MA, MT, MX, MY, NI, NL, NO, NZ, OM, PA, PE, PH, PK, PL, PT, PY, QA, RO, RS, SA, SE, SG, SI, SK, SV, TH, TR, TW, UA, UY, VE, VN, ZA
Quantity	248,167

Product

Slip-Cath Beacon Tip Catheter. Angiographic catheter. For use in angiographic procedures as a conduit for the delivery of contrast media and can help physicians diagnose occlusion or stenosis. The catheters are designed for percutaneous introduction into the vascular system over an appropriately sized wire guide.

Reason for recall

Reports of catheter tip splits and or separation. Loss of device function, medical intervention to retrieve separated segment, or complications resulting from separated tip occluding blood flow to end organs may result.

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-2319-2015. 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.