# FDA recall Z-0115-2020

> **GE Healthcare, LLC** · Class II · device recall initiated 2019-07-19.

## Product

Aestiva 7900, Model Numbers:  a) 1006-9300-000  b) 1006-9305-000   c) 1006-9118-000   d) 1006-9112-000   e) 1006-9113-000   f) 1006-9020-000   g) 1006-9033-000   h) 1006-9117-000   i) 1006-9119-000   j) 1006-9030-000   k) 1006-9032-000   l) 1006-9022-000   m) To be provided   n) 1006-9120-000   o) 1006-9027-000   p) 1006-9003-000   q) 1006-9025-000

## Reason for recall

Certain Aespire and Aestiva Anesthesia Systems were noted to have a vulnerability to a cyber-attack when connected to the hospital network.  An insufficiently secured terminal server may provide an opportunity for a malicious actor that has already penetrated the hospital network to send fraudulent flow sensor correction parameters.

## Distribution

Worldwide

## Key facts

- **Recall number:** Z-0115-2020
- **Recalling firm:** GE Healthcare, LLC
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2019-07-19
- **Report date:** 2019-12-25
- **Termination date:** 2026-04-13

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Waukesha, WI, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0115-2020

## Citation

> AI Analytics. FDA recall Z-0115-2020. Retrieved 2026-06-24 from https://api.ai-analytics.org/recall/Z-0115-2020. Source: US FDA. Licensed CC0.

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