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 400868 and 405652 with listed 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 with specific lidocaine and bupivacaine injections because quality issues were found during an FDA inspection. This recall affects medical devices used in spinal procedures.
The recall is due to quality deficiencies identified during an FDA manufacturing inspection, specifically related to acceptance testing. These issues could potentially affect the safety and reliability of the product during use.
Healthcare professionals using spinal anesthesia equipment are most likely affected. Patients receiving spinal anesthesia with these specific products may be impacted.
Check for catalog numbers 400868 or 405652 on the product packaging. The expiration dates for affected units range from October 2026 to January 2027.
Look for catalog numbers 400868 or 405652 on the product packaging.
The recall is due to quality issues identified during an FDA manufacturing facility inspection, specifically related to acceptance testing.
Spinal trays with lidocaine HCL (1%), 5 mL, bupivacaine HCL (0.75%) with dextrose, catalog numbers 400868 and 405652.
Check for catalog numbers 400868 or 405652 on the product packaging. Affected units have expiration dates from October 2026 to January 2027.
We’ve drafted a message you can send Becton Dickinson to request your refund or repair — edit it as you like.
Subject: Recall Z-2252-2026 — Becton Dickinson Becton Dickinson Hello, I own a Becton Dickinson that is covered by recall Z-2252-2026 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.
