Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

Open, Classified

BD Recanalization System, REF: BDRECANSYSTEM

FDA Recall Z-0676-2024 · Posted 2024-01-05

Recall StatusOpen, Classified
Product CodePDU
Date Initiated2023-11-14
Product Quantity403

Reason for Recall

Recanalization systems may be in a manufacturing mode that allows the system to continuously run without the typical 30 second pauses, and 4-minute warning/5-minute restart required messages to indicate the ten-minute maximum catheter use time has been exceeded, which may increase the risk of the device overheating or breaking.

Firm Action

On 11/14/23 recall notices were mailed and emailed to customers who were asked to do the following: 1) Discontinue use of affected product and immediately quarantine until ready to return for service activities. 2) Share this notification with all device users within your facility and network to ensure they are aware of this field action. This notification should also be shared with any organization where the potentially affected devices have been transferred. 3) Complete and return the response form via email to [email protected] 4) Recalling firm will contact customers to coordinate product return for service. Customers with questions can call the firm's North American Regional Complaint Center at 1-844-823-5433, Say "Recall" when prompted M-F 8am - 5pm CT, or email [email protected]

Root Cause

Process design

Distribution Pattern

US: CA, OH, PA, NY, TX, NJ, MS, IL, GA, AL, AZ, NC, NV, PR, IN, MA, WI, KS, AR, FL, MD, IA, NE, LA, HI, MO, DE, DC, VA, NM, CO, KY, ME, MN

Related FDA 510(k) Records

Devices referenced by this recall via K-numbers.

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

↑