Becton Dickinson recalls spinal trays with specific lidocaine and bupivacaine solutions due to quality issues found during FDA facility inspections. Affected units have catalog numbers 405645 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 solutions because quality problems were found during an FDA inspection. This recall affects medical devices used in spinal procedures, but the issue does not involve immediate safety risks to users.
The recall is due to quality deficiencies identified during an FDA facility inspection, specifically related to acceptance testing. These issues could potentially affect the accuracy of the product's quality control but do not pose an immediate risk to patient safety during normal use.
Healthcare professionals using spinal anesthesia equipment are most likely affected. Patients receiving this specific spinal tray during procedures may be impacted if the device is used.
Check for catalog number 405645 on the spinal tray. The expiration date is listed as October 2026 (lot number B01V223D).
Look for catalog number 405645 and expiration date October 2026 on the spinal tray.
The recall is due to quality issues identified during an FDA manufacturing facility inspection, specifically related to acceptance testing.
The official recall notice does not specify a remedy or action steps for affected users.
The recall indicates quality deficiencies but does not state that the product poses an immediate safety risk during normal use.
We’ve drafted a message you can send Becton Dickinson to request your refund or repair — edit it as you like.
Subject: Recall Z-2251-2026 — Becton Dickinson Becton Dickinson Hello, I own a Becton Dickinson that is covered by recall Z-2251-2026 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.
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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.
