Becton Dickinson & Company 2026-06-10 Health critical FDA
Health · FDA · Recall #FDA-Z-2251-2026
BD¿Spinal Tray with BD¿Whitacre Needle 22 G x 3.5 in.; lidocaine HCL (1%), 5 mL,… Recall
Issued June 10, 2026 · Becton Dickinson & Company
In June 2026, Becton Dickinson & Company recalled the BD¿Spinal Tray with BD¿Whitacre Needle 22 G x 3.5 in.; lidocaine HCL (1%), 5 mL,…, a critical health recall reported by the FDA. Affected owners are eligible for a voluntary. Here is what the hazard is and exactly what to do about it.
Compiled by Maya Ellison, RecallCheckr
What this means for you
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.
What you should do
- 1 Stop using BD¿Spinal Tray with BD¿Whitacre Needle 22 G x 3.5 in.; lidocaine HCL (1%), 5 mL,… right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact Becton Dickinson & Company to arrange your voluntary. See the official notice below for contact details.
- 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):
Recall details
- Brand
- Becton Dickinson & Company
- Category
- Health
- Recall date
- June 10, 2026
- Units affected
- Not reported
- Sold at
- Nationwide distribution to AK, AL, AR, AZ, CA, CO, CT, FL, GA, IA, IL, IN, KS, KY, LA, MA, MD, MI, MO, MS, NC, NE, NH, NJ, NV, NY, OH, OR, P
- Recall number
- FDA-Z-2251-2026
- Made in
- United States
- Issuing agency
- FDA
In context
- Becton Dickinson & Company has 6 recalls in our database, including 2 rated Critical.
- We're tracking 3,576 Health recalls in our database.
- This is the 356th Health recall we've logged in 2026.