# FDA recall Z-2958-2018

> **Covidien LLC** · Class II · device recall initiated 2018-07-26.

## Product

Li-ion battery packs used in BIS Vista and BIS View Monitoring Systems.  Product Number/CFN: 186-0208  UDI-Device Identifier (GTIN/UPN): 10884521130319

## Reason for recall

Revised replacement instructions for the Li-ion battery packs used in BIS Vista and BIS View Monitoring Systems

## Distribution

Nationwide  Foreign: Australia, New Zealand

## Key facts

- **Recall number:** Z-2958-2018
- **Recalling firm:** Covidien LLC
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2018-07-26
- **Report date:** 2018-09-05

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** North Haven, CT, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2958-2018

## Citation

> AI Analytics. FDA recall Z-2958-2018. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-2958-2018. Source: US FDA. Licensed CC0.

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