---
title: "Halyard CARDIAC CATH PACK kit. Model Number: EAMC1000-05, WAFB208-02. — FDA record Z-1970-2026 | Is It on Recall"
description: "Potential risk for Medline syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe a"
url: https://isitonrecall.com/recall/fda-device-z-1970-2026-halyard-cardiac-cath-pack-kit-model-number-eamc1000-05-wafb208-02/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / FDA device enforcement

# Halyard CARDIAC CATH PACK kit. Model Number: EAMC1000-05, WAFB208-02. — FDA record Z-1970-2026

Reported ongoing

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date Mar 13, 2026. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## What the record says

- **Product**: Halyard CARDIAC CATH PACK kit. Model Number: EAMC1000-05, WAFB208-02.
- **Reason**: Potential risk for Medline syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.
- **Classification**: Class I
- **Recalling firm**: AVID Medical, Inc.
- **Quantity**: 222 kits
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-1970-2026

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1970-2026%22)

[What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). Classification is an agency assessment, not individual medical advice.

## Lot and product identifiers

| Label field | Details supplied by the agency |
| --- | --- |
| Lot, code or applicability | 1. Model Number: EAMC1000-05. UDI-DI (Kit Lot Numbers): 10809160377314 (1573593, 1583827, 1609541, 1609725, 1612134, 1612516, 1619132, 1623384, 1627013, 1635459, 1672306, 1675159). 2. Model Number: WAFB208-02. UDI-DI (Kit Lot Numbers): 10809160424759 (1615954, 1653009). |

Match all identifying details in the current notice. A brand name alone is not enough.

## Distribution

US distribution to FL, IL, MO, MS, NC, NE, TX.

States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

- [Florida](https://isitonrecall.com/state/florida/)
- [Illinois](https://isitonrecall.com/state/illinois/)
- [Missouri](https://isitonrecall.com/state/missouri/)
- [Mississippi](https://isitonrecall.com/state/mississippi/)
- [North Carolina](https://isitonrecall.com/state/north-carolina/)
- [Nebraska](https://isitonrecall.com/state/nebraska/)
- [Texas](https://isitonrecall.com/state/texas/)

## Dates in the source

- **Report date**: May 13, 2026
- **Recall initiation date**: Mar 13, 2026
- **Center classification date**: May 1, 2026

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

## What to do next

Read the official notice for the action that applies to your exact product.

[Read the current instructions](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1970-2026%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [AVID Medical, Inc. records](https://isitonrecall.com/brand/avid-medical-inc/)