Synthroid (levothyroxine sodium) Tablets USP, 75 mcg, Rx Only, 90-Count Bottle, Abbott Laboratories, North Chicago, IL 60064, NDC: 0074-5182-90.
Reported: October 3, 2012 Initiated: July 19, 2012 #D-1695-2012
Product Description
Synthroid (levothyroxine sodium) Tablets USP, 75 mcg, Rx Only, 90-Count Bottle, Abbott Laboratories, North Chicago, IL 60064, NDC: 0074-5182-90.
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.
Details
- Recalling Firm
- Abbott Laboratories
- Units Affected
- 42,596 Bottles
- Distribution
- Nationwide
- Location
- Abbott Park, IL
Frequently Asked Questions
What product was recalled? ▼
Synthroid (levothyroxine sodium) Tablets USP, 75 mcg, Rx Only, 90-Count Bottle, Abbott Laboratories, North Chicago, IL 60064, NDC: 0074-5182-90.. Recalled by Abbott Laboratories. Units affected: 42,596 Bottles.
Why was this product recalled? ▼
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.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on October 3, 2012. Severity: Moderate. Recall number: D-1695-2012.
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