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 405671 and UDI numbers starting with (01)00382904056711.
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 lidocaine and bupivacaine solutions because quality issues were found during an FDA facility inspection. This recall affects medical professionals using these products for spinal procedures.
The recall is due to quality deficiencies identified during an FDA manufacturing facility inspection. These issues relate to acceptance testing, which could affect product safety but do not indicate immediate risk of serious injury.
Medical professionals who use the recalled spinal trays for spinal procedures are most at risk. The recall affects specific units with catalog number 405671 and UDI numbers starting with (01)00382904056711.
Check for catalog number 405671 on the spinal tray. Look for UDI numbers starting with (01)00382904056711. The lot number and expiration date are B01V275D (2027-01-01) or B01V294D (2027-01-01).
Look for catalog number 405671 and UDI numbers starting with (01)00382904056711 on the spinal tray.
The recall is due to quality issues identified during an FDA manufacturing facility inspection, specifically related to acceptance testing.
The affected product has catalog number 405671.
UDI numbers starting with (01)00382904056711 are affected.
We’ve drafted a message you can send Becton Dickinson to request your refund or repair — edit it as you like.
Subject: Recall Z-2256-2026 — Becton Dickinson Becton Dickinson Hello, I own a Becton Dickinson that is covered by recall Z-2256-2026 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.
