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Bound Tree Medical, LLC

Complete recall history across all FDA and CPSC categories — 6 total recalls

Bound Tree Medical, LLC appears in recall records across 1 category. This page consolidates all FDA food, drug, and medical device enforcement actions, plus CPSC consumer product recalls associated with this company. Recall data is sourced from openFDA and CPSC public databases.

Drug Recalls (6)

FDA drug safety enforcement actions by Bound Tree Medical, LLC

Date Product Reason Class
Nov 2, 2018 curaplex Epi Safe Kit, 8600-01101, contains:" 1ml Vial of Epinephrine " 1 Ep... Labeling Incorrect Instructions: This recall has been initiated because the ... Class II
Nov 2, 2018 curaplex Epi Safe Administration and Training Kits, #8600-01100, Contains: 2 ... Labeling Incorrect Instructions: This recall has been initiated because the ... Class II
Nov 2, 2018 Curaplex Epi Safe Kit, 8600-01102 TRAINING ONLY, Rx Only, Distributed by Sarn... Labeling Incorrect Instructions: This recall has been initiated because the ... Class II
Nov 2, 2018 Curaplex Epi Kit NOT FOR IV USE, #8600-01120, Epi-Safe Kit 8600-01 120 contai... Labeling Incorrect Instructions: This recall has been initiated because the ... Class II
Nov 1, 2018 Curaplex Epi Safe Kit, Rx Only, contains: 1mL Vial of Epinephrine, 1 Epi-Safe... Labeling: Incorrect or missing Lot and/or Exp Date:The Kit is incorrectly lab... Class III
Nov 1, 2018 curaplex Epi Safe Administration and Training Kits # 8600-01100. Kit contains... Labeling: Incorrect or Missing Lot and/or Exp date: vials of epinephrine wit... Class II

Frequently Asked Questions

A high number of recalls does not necessarily indicate that a company is unsafe. Large manufacturers that produce thousands of products across multiple categories will statistically appear in recall databases more frequently. What matters more is the severity of each recall (Class I being the most serious), the speed of response, and whether the company proactively identified and addressed the issue. Companies with robust safety programs often catch problems earlier.

Food, drug, and medical device recall data comes from the FDA's openFDA enforcement database, which contains all FDA enforcement reports. Consumer product recall data comes from the U.S. Consumer Product Safety Commission (CPSC). Both sources are public government databases that are updated regularly. RecallCheck aggregates these sources to provide a unified view of a company's recall history.

The FDA classifies recalls into three categories. Class I is the most serious — there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. Class II means the product may cause temporary or medically reversible health problems, or the probability of serious consequences is remote. Class III is the least serious — the product is unlikely to cause adverse health consequences. CPSC product recalls do not use this classification system.

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