Becton Dickinson recalls spinal trays with specific lidocaine and bupivacaine solutions due to quality deficiencies found during FDA facility inspections. Affected units have catalog numbers 405621 and 405735 with specific expiration dates.
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 that include lidocaine and bupivacaine solutions because quality issues were found during an FDA inspection. This recall affects specific catalog numbers with particular expiration dates. The issue relates to the manufacturing process, not the product's intended use.
The recall is due to quality deficiencies identified during an FDA manufacturing facility inspection. These deficiencies relate to acceptance testing procedures, which could affect the product's safety and effectiveness. However, the product is not expected to cause immediate harm under normal use conditions.
Healthcare professionals using spinal anesthesia equipment are most likely affected. The recall targets specific units with catalog numbers 405621 and 405735 that were manufactured with specific expiration dates.
Check for catalog numbers 405621 or 405735 on the spinal tray packaging. The units have specific expiration dates: June 1, 2026, or October 1, 2026, depending on the catalog number.
Identify the catalog number and expiration date on the spinal tray packaging to confirm if it is affected.
The recall is due to quality deficiencies identified during an FDA manufacturing facility inspection, specifically related to acceptance testing.
The product has quality issues related to acceptance testing procedures, which could affect its safety and effectiveness.
Check for catalog numbers 405621 or 405735 with expiration dates of June 1, 2026, or October 1, 2026.
We’ve drafted a message you can send Becton Dickinson to request your refund or repair — edit it as you like.
Subject: Recall Z-2249-2026 — Becton Dickinson Becton Dickinson Hello, I own a Becton Dickinson that is covered by recall Z-2249-2026 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.
