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 400866-406704 with specific lot numbers.
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 certain lidocaine and bupivacaine injections because quality problems were found during an FDA inspection. This recall affects specific catalog numbers and lot dates, but the issue does not pose an immediate safety risk to users.
The recall is due to quality deficiencies identified during an FDA manufacturing facility inspection. These issues relate to acceptance testing, which means the products may not meet the required quality standards for medical use.
Healthcare professionals who use these spinal trays for medical procedures may be affected. Patients receiving these injections are at risk if they use the recalled products.
Check for catalog numbers 400866, 405672, 405673, 405674, 405675, 405709, 405721, 405723, or 406704. The lot numbers and expiration dates listed in the recall notice indicate specific affected batches.
Review the catalog number and lot number on the product to see if it matches the listed affected items.
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, so no action is required beyond checking if your product matches the affected catalog numbers and lot dates.
The recall states quality deficiencies but does not mention a risk of injury or harm to users.
We’ve drafted a message you can send Becton Dickinson to request your refund or repair — edit it as you like.
Subject: Recall Z-2255-2026 — Becton Dickinson Becton Dickinson Hello, I own a Becton Dickinson that is covered by recall Z-2255-2026 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.
