Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
curaplex Epi Safe Administration and Training Kits # 8600-01100. Kit Recalled by Bound Tree Medical, LLC Due to Labeling: Incorrect or Missing Lot and/or Exp date:...
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 Bound Tree Medical, LLC directly.
Affected Products
curaplex Epi Safe Administration and Training Kits # 8600-01100. Kit contains 2 Epi Safe Administration Kit (8600-01101) and 1 Epi Safe Training Kit (8600-01102), Rx Only. Distributed by Sarnova HC, LLC's family of companies: Bound Tree Medical, LLC, Cardio Partners, Inc., Emergency Medical Producs, Inc. & Tri-anim Health Services, Inc. 5000 Tuttle Crossing Blvd, Dublin, OH 43016
Quantity: 84 kits
Why Was This Recalled?
Labeling: Incorrect or Missing Lot and/or Exp date: vials of epinephrine within kit 8600-01100 expired on December 2018, but the outer kit label has an expiration date of January 2020. In addition, device component (syringe) may lack 510(k) clearance.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Bound Tree Medical, LLC
Bound Tree Medical, LLC has 6 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report