Becton Dickinson recalls spinal trays with specific needle and anesthetic mixtures due to quality issues found during FDA facility inspections. Affected units have catalog numbers 405632 and UDI numbers starting with (01)00382904056322.
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 mixtures because quality issues were found during an FDA facility inspection. This recall affects medical devices used in spinal procedures.
Quality deficiencies were identified during an FDA inspection related to acceptance testing. These issues could potentially affect the safety and reliability of the spinal tray during medical procedures, though no specific injury mechanism is described.
Healthcare professionals using spinal anesthesia equipment are most likely affected. The recall targets specific units with catalog number 405632 and UDI numbers starting with (01)00382904056322.
Check for catalog number 405632 on the spinal tray. Look for UDI numbers starting with (01)00382904056322. The lot number (B01V231D) expires January 1, 2027, and a newer version (B02V248D) expires January 1, 2027.
Look for catalog number 405632 and UDI numbers starting with (01)00382904056322 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 405632.
UDI numbers starting with (01)00382904056322 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-2250-2026 — Becton Dickinson Becton Dickinson Hello, I own a Becton Dickinson that is covered by recall Z-2250-2026 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.
