# FDA recall D-0955-2017

> **Advanced Pharma Inc.** · Class II · drug recall initiated 2017-06-22.

## Product

Potassium Phosphate (USP) QS 0.9% Sodium Chloride (USP) 250 mL 30 mmol in NS 250mL Bag, Advanced Pharma, 9265 Kirby Dr., Houston, TX 77054 (877) 794-0404. NDC15082-924-25

## Reason for recall

Lack of Assurance of Sterility

## Distribution

Nationwide with the United States

## Key facts

- **Recall number:** D-0955-2017
- **Recalling firm:** Advanced Pharma Inc.
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2017-06-22
- **Report date:** 2017-07-19
- **Termination date:** 2017-12-06

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Houston, TX, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0955-2017

## Citation

> AI Analytics. FDA recall D-0955-2017. Retrieved 2026-06-26 from https://api.ai-analytics.org/recall/D-0955-2017. Source: US FDA. Licensed CC0.

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*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*
