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 405637 and 405707 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 come with lidocaine and bupivacaine injections because quality problems were found during an FDA inspection. This recall affects specific product versions with catalog numbers 405637 and 405707 that were manufactured with certain expiration dates.
The recall is due to quality issues identified during an FDA manufacturing facility inspection. These issues relate to specific acceptance testing procedures that could affect the product's safety and effectiveness.
Healthcare professionals using these spinal trays for medical procedures are most at risk. Patients receiving these injections during surgery or procedures may be affected if the product is used without the recall being addressed.
Check for catalog numbers 405637 or 405707 on the spinal tray packaging. The product includes lidocaine HCL (1%), 5 mL, bupivacaine HCL (0.75%) with dextrose (8.25%), 2 mL. Expiration dates range from June 2026 to January 2027.
Look for catalog numbers 405637 or 405707 on the spinal tray packaging to confirm if it is affected.
The product was recalled 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 products.
Affected products have expiration dates from June 2026 to January 2027, including specific lot numbers.
We’ve drafted a message you can send Becton Dickinson to request your refund or repair — edit it as you like.
Subject: Recall Z-2257-2026 — Becton Dickinson Becton Dickinson Hello, I own a Becton Dickinson that is covered by recall Z-2257-2026 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.