# FDA recall D-1694-2012

> **Abbott Laboratories** · Class II · drug recall initiated 2012-07-19.

## Product

Synthroid (levothyroxine sodium) Tablets USP, 50 mcg, Rx Only, 90-Count Bottle, Abbott Laboratories, North Chicago, IL 60064, NDC: 0074-4552-90.

## Reason for recall

Defective Container: A number of Synthroid bottles have a localized thin wall defect on the bottom which may potentially impact the stability of the tablets.

## Distribution

Nationwide

## Key facts

- **Recall number:** D-1694-2012
- **Recalling firm:** Abbott Laboratories
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2012-07-19
- **Report date:** 2012-10-03
- **Termination date:** 2013-11-01

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

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-1694-2012

## Citation

> AI Analytics. FDA recall D-1694-2012. Retrieved 2026-05-25 from https://api.ai-analytics.org/recall/D-1694-2012. Source: US FDA. Licensed CC0.

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