# FDA recall D-088-2013

> **Genentech Inc** · Class II · drug recall initiated 2012-09-20.

## Product

Nutropin AQ NuSpin 10 (somatropin (rDNA origin) injection} 10 mg/ 2mL Genentech, South San Francisco, CA 94080, NDC#50242-0074-01

## Reason for recall

Miscalibrated and/or Defective Delivery System: Genentech has received complaints  for Nutropin AQ NuSpin 10 & 20  reporting that the dose knob spun slowly and the injection took longer than usual (slow dose delivery).

## Distribution

Nationwide

## Key facts

- **Recall number:** D-088-2013
- **Recalling firm:** Genentech Inc
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2012-09-20
- **Report date:** 2012-12-12
- **Termination date:** 2013-12-24

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** South San Francisco, CA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-088-2013

## Citation

> AI Analytics. FDA recall D-088-2013. Retrieved 2026-05-25 from https://api.ai-analytics.org/recall/D-088-2013. Source: US FDA. Licensed CC0.

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