Bound Tree Medical, LLC recalls Curaplex Epi Safe Kit, Rx Only, contains: 1mL Vial of Epinephrine, 1 Epi-Safe Syringe, 1 Safety needle, 2 Alcohol Prep…
- Recall date
- November 1, 2018
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- D-0379-2019
- FDA classification
- Class III
- Brand / firm
- Bound Tree Medical, LLC
- Sold / distributed
- Nationwide in the USA
Why it was recalled
Labeling: Incorrect or missing Lot and/or Exp Date:The Kit is incorrectly labeled as expiring May 2018 however the correct expiration date is May 2019. In addition, device component (syringe) lacks 510(k) clearance.
Class III means the product violates regulations but is not likely to cause harm.
What was recalled
Curaplex Epi Safe Kit, Rx Only, contains: 1mL Vial of Epinephrine, 1 Epi-Safe Syringe, 1 Safety needle, 2 Alcohol Prep Pads,1 Adhesive Dressing, 1 Insert. Distributed by Sarnova, HC. LLC's family companies: Bound Tree Medical. LLC, Cardio Partners, Inc., Emergency Medical Products, Inc. & Tri-amin Health Services, Inc. 5000 Tuttle Crossing Blvd, Dublin, OH 43016. Model 8600-01101
Get recall alerts
Free email alert whenever Bound Tree Medical, LLC has a new recall — straight from official government data. Unsubscribe anytime.
More recalls from: Bound Tree Medical, LLC