# FDA recall D-0030-2018

> **Baxter Healthcare Corporation** · Class I · drug recall initiated 2017-09-15.

## Product

Intralipid 20%, A 20% I.V. Fat Emulsion, 100 ml bag, Rx only, Manufactured by Fresenius Kabi, Uppsala, Sweden for Baxter Healthcare Corporation, Deerfield, IL 60015 USA, NDC 0338-0519-58

## Reason for recall

Temperature Abuse: A portion of this product lot was exposed to subfreezing temperatures, which is outside of the acceptable storage range listed on the product labeling, during transit to a distribution facility.

## Distribution

Impacted shipment sent to Wholesalers, Medical Facilities and Physicians in CA and NV, but could have been further distributed Nationwide in the USA.

## Key facts

- **Recall number:** D-0030-2018
- **Recalling firm:** Baxter Healthcare Corporation
- **Classification:** Class I
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2017-09-15
- **Report date:** 2017-11-01
- **Termination date:** 2018-09-06

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Deerfield, IL, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0030-2018

## Citation

> AI Analytics. FDA recall D-0030-2018. Retrieved 2026-06-23 from https://api.ai-analytics.org/recall/D-0030-2018. Source: US FDA. Licensed CC0.

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