No image published for this recall

Bard ep xt decapolar steerable, diagnostic ep catheter, 6f, large 4.0, 10, 2-5-2mm, ref: 201007

Official notice

14 Oct 2026

Last checked

20 Oct 2026

MediumFDA

An official FDA notice concerns Stryker Sustainability. The notice reports an infection risk. Stop using the product and follow the official notice. Published 2026-10-14. Recall numbers: Z-0085-2027. Check the official notice for the complete list.

What to do now

Instructions for consumers are available in the official FDA notice.

Units affected

10

Recall number

Z-0085-2027

Official notice

2026-10-14

The hazard

Infection risk

How to check if you're affected

Compare the product name and identifiers below with the item you own. Follow the official notice if they match.

Other

UDI-DI 00885825003838

Event Ids

99655

Recall Numbers

Z-0085-2027

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Where it was sold

The source does not list specific retailers. See the official notice for where affected products were sold.

Location 1

US · United States

Affected area 1

US · United States

Company & contacts

Manufacturer

Not provided

Phone

Not provided

Brand: Stryker Sustainability. Contact: Stryker Sustainability Solutions.

Source & status

Source

Tier

official

Category

ELECTRONICS

Classification

Class II

App estimate

medium

Recall details

Recall number

Z-0085-2027

Event id

99655

Units affected

10

Status

active

Classification

Class II

Source tier

official

Documents, notices & source

See the official notice and source documents for full details.

View full official notice
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