Serious health hazard — there is a reasonable probability that use of or exposure to this product will cause serious adverse health consequences or death.
BRILINTA (ticagrelor) tablets Recalled by AstraZeneca Pharmaceuticals, LP Due to Presence of Foriegn Tablets/Capsules: customer complaint that an...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact AstraZeneca Pharmaceuticals, LP directly.
Affected Products
BRILINTA (ticagrelor) tablets, 90 mg, 8-count Professional Sample bottles, Rx only, Mfd. for: AstraZeneca Pharmaceuticals LP, Wilmington, DE 19850; By: AstraZeneca AB, SE-151 85 Sodertalje, Sweden, NDC 0186-0777-08.
Quantity: 40,368 bottles
Why Was This Recalled?
Presence of Foriegn Tablets/Capsules: customer complaint that an 8-count professional sample bottle labeled as BRILINTA 90 mg tablets contained 5 ZURAMPIC 200 mg tablets, in addition to the expected 8 BRILINTA tablets.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About AstraZeneca Pharmaceuticals, LP
AstraZeneca Pharmaceuticals, LP has 1 total recall tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report