HIGH

BD Recalls 38 Veritor Connect Software Units Over Credential Access Risk (2025)

BD recalled 38 Veritor Connect Software units distributed to healthcare providers worldwide. Unauthorized access to product service credentials could affect confidentiality, integrity or availability of the product and data. Stop using the software and follow the recall instructions provided by the manufacturer.

Quick Facts at a Glance

Recall Date
September 23, 2025
Hazard Level
HIGH
Brand
BD
Category
Health & Personal Care
Sold At
Multiple Retailers
Geographic Scope
1 states
At-Risk Groups
GENERAL

Hazard Information

Product service credentials used by some BD technical support teams to access certain BD products were accessed by an unauthorized actor. Until these product service credentials are updated, there is a risk of unauthorized access that may impact the confidentiality, integrity and/or availability of the relevant products and associated data.

What You Should Do

Patients and healthcare providers should stop using this device immediately. Follow the recall instructions provided by the manufacturer. Contact Becton Dickinson & Co. or your healthcare provider for instructions. Notification method: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

Get instant alerts for Health & Personal Care recalls

Be the first to know. Free instant alerts to your inbox.

No spamUnsubscribe anytime

About This Product

BD Veritor Connect Software transfers in vitro diagnostic results data from the BD Veritor Plus Analyzer to the BD Synapsys platform.

Why This Is Dangerous

An unauthorized actor gaining access to product service credentials could compromise data confidentiality, integrity and availability of the affected BD Veritor systems.

Industry Context

This recall is not identified as part of a broader industry pattern.

Real-World Impact

No injuries reported. The issue centers on data security and access controls rather than physical device failure.

Practical Guidance

How to identify if yours is affected

  1. Verify catalog number 444881.
  2. Cross-check the UDI 00382904448813.
  3. Review serial numbers list for SL codes.

Where to find product info

On device labels, packaging or recall notices from BD and FDA.

What timeline to expect

Refunds or replacements typically processed within 4-6 weeks after submission of the claim.

If the manufacturer is unresponsive

  • Escalate to BD's recall case management.
  • File a complaint with the FDA if BD is nonresponsive.
  • Document all communications and dates.

How to prevent similar issues

  • Implement strict credential management for service accounts.
  • Regularly update credentials and monitor access logs.
  • Apply security patches and firmware updates promptly.

Documentation advice

Keep copies of the recall notice, screenshots of communications, and any purchase details for your records.

Product Details

Catalog Number: 444881. Serial numbers include SL00087, SL00098, SL01320, SL00083, SL00089, SL01002, SL01050, SL01522, SL00095, SL01480, SL01000, SL00551, SL01007, SL00062, SL01354, SL00097, SL01028, SL00066. UDI/DI: 00382904448813. Distribution: Worldwide. Quantity recalled: 38 units.

Reported Incidents

No injuries or incidents have been reported.

Key Facts

  • 38 units recalled
  • Catalog Number: 444881
  • UDI/DI: 00382904448813
  • Serial Numbers: SL00087, SL00098, SL01320, SL00083, SL00089, SL01002, SL01050, SL01522, SL00095, SLÅ
  • faulty list continues

Safety Guide

Not sure what to do next? Our guide walks you through the process step by step.

Read: What to Do When You Find a Recalled Product

Get Alerts for Health & Personal Care Recalls

Get instant alerts for recalls that affect you. Free forever.

Safety Assessment

Risk LevelHIGH
Severity Score
8/ 10
Affected Groups
GENERAL
Injury Types
OTHER

Product Classification

Product TypeBD Veritor Connect Software
Sold At
Multiple Retailers

Product Details

Brand
Model Numbers
Catalog Number (Serial Numbers): 444881
UDI/DI: 00382904448813
SL00087
SL00098
SL01320
+15 more
Affected States
ALL
Report Date
October 29, 2025
Recall Status
ACTIVE

Related Recalls

Health & Personal Care
HIGH

BD Recalls 62 BD MAX System IVD Units Worldwide Over Credential Breach (2025)

BD MAX System recall affects 62 units distributed worldwide in 2025 after unauthorized access to service credentials. An unauthorized actor accessed credentials used by BD technical support teams. Healthcare providers should stop using the devices and follow the manufacturer’s recall instructions.

BD
Product service
Read more
Health & Personal Care
HIGH

BD Phoenix M50 Recall: 4,283 Systems Worldwide Over Access Risk (2025)

BD recalled 4,283 Phoenix M50 Automated Microbiology Systems worldwide after unauthorized access to product service credentials. The unauthorized actor could access affected products and data. Labs should stop using these devices and follow the recall instructions from BD; contact BD for remediation guidance.

BD
Product service
Read more
Health & Personal Care
HIGH

CareFusion 303 BD Alaris Infusion Sets Recalled for Flow, Bolus Accuracy Issues (2025)

CareFusion 303 BD Alaris infusion pump modules and compatible infusion sets are recalled nationwide in the U.S. and multiple international markets. The recall covers reference numbers including C24101E and 10015414 and related SmartSite components. The defect may cause flow rate and bolus accuracy deviations, and incorrect occlusion timing. Stop using the device and follow recall instructions from

CareFusion
Infusion pump
Read more