Becton Dickinson recalls spinal trays with specific lidocaine and bupivacaine injections due to quality issues found during FDA facility inspections. Affected units have catalog numbers 405658 and expiration dates up to October 2026.
This is a sub-recall of a product recall from Huons Co, Ltd., the manufacturer of Bupivacaine Hydrochloride in Dextrose Injection, USP. The recall is due to quality issues identified during an FDA manufacturing facility inspection, citing specific quality deficiencies related to acceptance testing.
Becton Dickinson is recalling spinal trays with specific anesthetic injections because quality problems were found during an FDA inspection. This recall affects medical devices used in spinal procedures, but no injuries have been reported.
Quality issues were identified during an FDA facility inspection related to acceptance testing. This means the products may not meet safety standards for medical use, though no injuries have been reported.
Healthcare professionals using spinal anesthesia equipment are most at risk. The recall targets specific medical devices sold for spinal procedures.
Check for catalog number 405658 on the spinal tray packaging. The expiration date on the lot number is October 2026 (B01V217D).
Look for catalog number 405658 and expiration date B01V217D (October 2026) on the packaging.
The recall is due to quality issues identified during an FDA manufacturing facility inspection, specifically related to acceptance testing.
The recall is for quality issues found during an FDA inspection, but no injuries have been reported.
Check for catalog number 405658 and expiration date B01V217D (October 2026) on the packaging.
We’ve drafted a message you can send Becton Dickinson to request your refund or repair — edit it as you like.
Subject: Recall Z-2254-2026 — Becton Dickinson Becton Dickinson Hello, I own a Becton Dickinson that is covered by recall Z-2254-2026 from Becton Dickinson. 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
