Drug recall D-1695-2012
Product
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.
Lots and codes
Lot: 18353A8, Exp 08/31/2013
Recall details
- Recalling firm
- Abbott Laboratories, Abbott Park, IL
- Quantity
- 42,596 Bottles
- Distribution
- Nationwide
- Type
- Voluntary: Firm initiated
- Recall initiated
- July 19, 2012
- Terminated
- November 1, 2013
Related products
- Synthroid – drug information
- NDC 0074-3727 Synthroid · Levothyroxine Sodium 137 ug/1 · AbbVie Inc.
- NDC 0074-7068 Synthroid · Levothyroxine Sodium 125 ug/1 · AbbVie Inc.
- NDC 0074-4552 Synthroid · Levothyroxine Sodium 50 ug/1 · AbbVie Inc.
- NDC 0074-6624 Synthroid · Levothyroxine Sodium 100 ug/1 · AbbVie Inc.
- NDC 0074-7149 Synthroid · Levothyroxine Sodium 300 ug/1 · AbbVie Inc.
- NDC 0074-6594 Synthroid · Levothyroxine Sodium 88 ug/1 · AbbVie Inc.
- NDC 0074-9296 Synthroid · Levothyroxine Sodium 112 ug/1 · AbbVie Inc.
- NDC 0074-7070 Synthroid · Levothyroxine Sodium 175 ug/1 · AbbVie Inc.
- NDC 0074-7069 Synthroid · Levothyroxine Sodium 150 ug/1 · AbbVie Inc.
- NDC 0074-7148 Synthroid · Levothyroxine Sodium 200 ug/1 · AbbVie Inc.
- NDC 0074-5182 Synthroid · Levothyroxine Sodium 75 ug/1 · AbbVie Inc.
- NDC 0074-4341 Synthroid · Levothyroxine Sodium 25 ug/1 · AbbVie Inc.