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Becton Dickinson Infusion Therapy Systems Inc.

Complete recall history across all FDA and CPSC categories — 4 total recalls

Becton Dickinson Infusion Therapy Systems Inc. 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.

Device Recalls (4)

FDA medical device enforcement actions by Becton Dickinson Infusion Therapy Systems Inc.

Date Product Reason Class
Oct 4, 2023 BD Insyte Autoguard BC Shielded IV Catheter with Blood Control Technology 20G... Over-the-needle, intravascular catheters may have needles that do not retract... Class II
Aug 29, 2023 REF: 386862, BD Cathena Safety IV catheter with BD Multiguard Technology, 20 ... There is the potential that the safety shield may not properly engage on IV c... Class II
Oct 12, 2022 BD Nexiva Closed IV Catheter System - Single Port REF 383516 20 GA X1.0o in (... During needle withdrawal, the tip shield may prematurely separate from the ca... Class II
Sep 8, 2021 BD Nexiva, 20 GA 1.00 IN (1.1 X 25 mm), 3660 ml/hr. 61ml/min; Closed IV Cathe... There is a breach in the product packaging that renders the product non-sterile. 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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