Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
RELPAX (eletriptan HBr) tablets Recalled by Pfizer Inc. Due to Microbial Contamination of Non-Sterile Products: contamination with Burkholderia...
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 Pfizer Inc. directly.
Affected Products
RELPAX (eletriptan HBr) tablets, 40 mg, packaged in a) 6-count (1 card x 6 tablets) per carton, NDC 0049-2340-45; b) 12-count (2 cards x 6 tablets) per carton, NDC 0049-2340-05, Rx only, Made in Ireland, Distributed by Pfizer Roerig, Division of Pfizer Inc., NY, NY 10017.
Quantity: a) 20,117 cartons; b) 2,502 cartons
Why Was This Recalled?
Microbial Contamination of Non-Sterile Products: contamination with Burkholderia and Pseudomonas.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Pfizer Inc.
Pfizer Inc. has 114 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report