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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.

Official notice
BDHealth & Personal CareMedical DevicesCatalog Number (Serial Numbers): 444881UDI/DI: 00382904448813SL00087

Source-backed recall notice

No product image was available from the source feed.

Official source
FDA DEVICE
Recall date
September 23, 2025
Status
ACTIVE
Severity
8/10

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

What to Do Now

Use this page like a recall checklist: verify the product first, then act on the official remedy.

Immediate steps

  1. 1Stop using the product until you confirm whether it is included in the recall.
  2. 2Compare the product label, model number, UPC, color, size, and purchase location against the identifiers below.
  3. 3Follow the official remedy from FDA - Medical Devices; save photos, receipts, labels, and correspondence before contacting the company.
  4. 4If the product could harm a child, older adult, pet, or patient, move it out of reach immediately.

Check these identifiers

Brand
BD
Product type
BD Veritor Connect Software
Model numbers
Catalog Number (Serial Numbers): 444881, UDI/DI: 00382904448813, SL00087, SL00098, SL01320, SL00083, SL00089, SL01002 +12 more
Sold at
Multiple Retailers
Where affected
ALL

Recall Timeline

Key dates and source checks for this recall record.

  1. Recall announced

    September 23, 2025

  2. Reported by FDA DEVICE

    October 29, 2025

  3. RecallRadar source check

    April 18, 2026

  4. Consumer action

    Use the official remedy and keep documentation.

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

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.

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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

  • 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

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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

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