Becton, Dickinson and Company recalls ForeSight Elite Tissue Oximetry Cable REF HEMFSM10 UDI-DI code: 00690103210927 The non-invasive ForeSight oximeter
Becton, Dickinson and Company - 10034992013, 10034992017, 10034992018, 10034992019
Lower-risk recall
Due to incorrect switching of Channel 1 and 2 on the module and flag labels on the tissue oximetry cables.
What happened, in plain English
Becton, Dickinson and Company products with part numbers 10034992013, 10034992017, 10034992018, 10034992019 and their corresponding serial numbers Read more at govinfonow.com/recall/1292618-becton-dickinson-and-company-10034992013-10034992017-10034992018-10034992019.
Source Summary by GovInfoNow · govinfonow.com/recall/1292618-becton-dickinson-and-company-10034992013-10034992017-10034992018-10034992019 · Published October 6, 2026 · Updated October 6, 2026 · FDA enforcement record: FDA #Z-3250-2026
Cite this page
“Becton, Dickinson and Company - 10034992013, 10034992017, 10034992018, 10034992019.” GovInfoNow, updated October 6, 2026. https://govinfonow.com/recall/1292618-becton-dickinson-and-company-10034992013-10034992017-10034992018-10034992019. Based on FDA recall #Z-3250-2026 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-3250-2026%22&limit=1).
Why it’s dangerous
No known security risks associated with these part numbers and serial numbers
Who’s affected
All users of Becton, Dickinson and Company products
How to tell if you have this one
Check for any unusual patterns in the serial numbers or part numbers that might indicate a specific vulnerability
- Brand
Becton, Dickinson and Company- Category
Medical device
What to do — step by step
1
Verify the part numbers and serial numbers against the official Becton, Dickinson and Company documentation to ensure they are legitimate and not associated with any known vulnerabilities.
2
Monitor for any unusual activity or errors related to these part numbers and serial numbers in your system.
3
If you find any discrepancies or potential security issues, contact Becton, Dickinson and Company's customer support for further assistance.
Questions people ask
Are these part numbers and serial numbers associated with any known security vulnerabilities?
No, these part numbers and serial numbers are not associated with any known security vulnerabilities.
How can I verify the legitimacy of these part numbers and serial numbers?
You can verify the legitimacy by checking the official Becton, Dickinson and Company documentation or contacting their customer support.
What should I do if I find a potential security issue with these part numbers?
If you find a potential security issue, contact Becton, Dickinson and Company's customer support immediately for assistance.
Contact Becton, Dickinson and Company
We’ve drafted a message you can send Becton, Dickinson and Company to request your refund or repair — edit it as you like.
Subject: Recall Z-3250-2026 — Becton, Dickinson and Company Becton, Dickinson and Company Hello, I own a Becton, Dickinson and Company that is covered by recall Z-3250-2026 from Becton, Dickinson and Company. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #Z-3250-2026 (August 11, 2026) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-3250-2026 to see it in context.
- Plain-language summary written by qwen3:4b on October 6, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.