Tikosyn¿ (dofetilide) 500 mcg (0.5mg) capsules, 60-count bottle, Rx only Pfizer Labs, Division of Pfizer Inc. NY, NY 10017, NDC 00069-5820-60
Reported: April 30, 2014 Initiated: April 8, 2014 #D-1253-2014
Product Description
Tikosyn¿ (dofetilide) 500 mcg (0.5mg) capsules, 60-count bottle, Rx only Pfizer Labs, Division of Pfizer Inc. NY, NY 10017, NDC 00069-5820-60
Reason for Recall
Presence of Foriegn Tablets/Capsules: A single Tikosyn¿ (dofetilide) 250 mcg capsule was discovered in one bottle of Tikosyn¿ (dofetilide) 500 mcg (0.5 mg).
Details
- Recalling Firm
- Pfizer Inc.
- Units Affected
- 23,064 bottles
- Distribution
- US Nationwide including Puerto Rico and US Virgin Islands. 65 federal government accounts received the affected product directly from Pfizer Inc
- Location
- N/A
Frequently Asked Questions
What product was recalled? ▼
Tikosyn¿ (dofetilide) 500 mcg (0.5mg) capsules, 60-count bottle, Rx only Pfizer Labs, Division of Pfizer Inc. NY, NY 10017, NDC 00069-5820-60. Recalled by Pfizer Inc.. Units affected: 23,064 bottles.
Why was this product recalled? ▼
Presence of Foriegn Tablets/Capsules: A single Tikosyn¿ (dofetilide) 250 mcg capsule was discovered in one bottle of Tikosyn¿ (dofetilide) 500 mcg (0.5 mg).
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on April 30, 2014. Severity: Moderate. Recall number: D-1253-2014.
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