FDA recall, , High risk
Becton Dickinson & Company BD Spinal Trays
BD Spinal Trays with Quincke or Whitacre needles have quality deficiencies related to acceptance testing.
What happened
Becton Dickinson & Company, of Franklin Lakes, New Jersey, recalled BD Spinal Trays with BD Whitacre or BD Quincke needles containing lidocaine HCL and bupivacaine HCL with dextrose.
The recall, which began April 27, 2026, is a sub-recall of a product recall from Huons Co, Ltd., the manufacturer of Bupivacaine Hydrochloride in Dextrose Injection, USP, due to quality deficiencies related to acceptance testing identified during an FDA manufacturing facility inspection. The affected products were distributed nationwide.
What to do
We don't have product-specific instructions for this recall. FDA's general advice for medical device recalls:
- A device recall doesn't always mean you must stop using it: it may need to be checked, adjusted or fixed.
- Talk to your health care provider before you stop using it.
Is yours affected?
Affected if its UDI-DI, lot code and catalog code are listed under that product.
A UDI-DI is the device identifier printed with the barcode on the device label.
BD¿Spinal Tray with BD¿Whitacre Needle 22 G x 3.5 in.; lidocaine HCL (1%), 5 mL, bupivacaine HCL (0.75%) with dextrose (8.25%), 2 mL (marcaine).
- UDI-DI
- 00382904056452
- Catalog code
- 405645.
- Lot code
- B01V223D
- 2026-10-01
BD¿Spinal Tray with BD¿Quincke Needle 26 G x 3.5 in.; lidocaine HCL (1%), 5 mL, bupivacaine HCL (0.75%) with dextrose (8.25%), 2 mL (marcaine).
- UDI-DI
- 00382904056322
- Catalog code
- 405632.
- Lot code
- B01V231D
- 2027-01-01
- B02V248D
BD¿Spinal Tray with BD¿Whitacre Needle 25 G x 3.5 in.; lidocaine HCL (1%), 5 mL, bupivacaine HCL (0.75%) with dextrose (8.25%), 2 mL (marcaine).
- UDI-DI
- 00382904056377
- 00382904057077
- Catalog code
- 405637
- 405707.
- Lot code
- B01V160D
- 2026-06-28
- B01V241D
- 2027-01-01
- B01V265D
- B02V183D
- 2026-10-01
- B02V230D
- UDI-DI
- 10885403469497
- 00382904056728
- 00382904056735
- 00382904056742
- 00382904056759
- 00382904057091
- 00382904057213
- 00382904057237
- 00382904067045
- Catalog code
- 400866
- 405672
- 405673
- 405674
- 405675
- 405709
- 405721
- 405723
- 406704.
- Lot code
- B01V232D
- 2027-01-01
- B03V267D
- B01V225D
- 2026-10-01
- B01V281D
- B02V211D
- B02V217D
- B01V218D
- B01V183D
- B01V198D
- 2026-09-01
- B02V202D
- B02V174D
- 2026-06-28
- B02V227D
- B01V174D
- B02V254D
- B01V189D
- B02V246D
- UDI-DI
- 00382904056711
- Catalog code
- 405671.
- Lot code
- B01V275D
- 2027-01-01
- B01V294D
BD¿Spinal Tray with BD¿Quincke Needle 25 G x 3.5 in.; lidocaine HCL (1%), 5 mL, bupivacaine HCL (0.75%) with dextrose (8.25%), 2 mL (marcaine).
- UDI-DI
- 00382904056216
- 00382904057350
- Catalog code
- 405621
- 405735.
- Lot code
- B01V142D
- 2026-06-01
- B01V176D
- 2026-06-28
- B01V149D
- B01V190D
- 2026-10-01
BD¿Spinal Tray with BD¿Whitacre Needle 25 G x 3.5 in.; lidocaine HCL (1%), 2 mL, bupivacaine HCL (0.75%) with dextrose (8.25%), 2 mL (marcaine).
- UDI-DI
- 00382904056582
- Catalog code
- 405658.
- Lot code
- B01V217D
- 2026-10-01
BD¿Spinal Tray with BD¿Whitacre Needle 25 G x 3.5 in., BD¿Quincke Needle 22 G x 3.5 in.; lidocaine HCL (1%), 5 mL, bupivacaine HCL (0.75%) with dextrose (8.25%), 2 mL (marcaine).
- UDI-DI
- 00382904057411
- Catalog code
- 405741.
- Lot code
- B02V204D
- 2026-10-01
BD¿Spinal Tray with BD¿Quincke Needle 22 G x 3.5 in.; lidocaine HCL (1%), 5 mL, bupivacaine HCL (0.75%) with dextrose (8.25%), 2 mL (marcaine).
- UDI-DI
- 00382904056094
- Catalog code
- 405609.
- Lot code
- B01V212D
- 2026-10-01
- B01V238D
- 2027-01-01
BD¿Spinal Tray with BD¿Whitacre Needle 24 G x 3.5 in.; lidocaine HCL (1%), 5 mL, bupivacaine HCL (0.75%) with dextrose (8.25%), 2 mL (marcaine).
- UDI-DI
- 10885403469510
- 00382904056520
- Catalog code
- 400868
- 405652.
- Lot code
- B01V206D
- 2026-10-01
- B01V220D
- B02V266D
- 2027-01-01
- B01V353D
- 2027-01-30
- B02V267D
Recall details
- Company began the recall
- Sold in
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, PA, PR, SD, TN, TX, UT, VA, WA, WI, WV, WY.
- Company
- Becton Dickinson & CompanyFranklin Lakes, New Jersey
- Hazard
- Device defect
- Risk
High risk
There is a reasonable chance that using it could cause serious health problems or death.
FDA Class I recall · How risk is rated
- Event ID
- 98842
- Recall numbers
- Z-2248-2026 to Z-2257-2026
All recalls from Becton Dickinson & Company
Timeline
FDA's Enforcement Report is its public list of recalls; FDA adds a recall when it posts it and publishes the list weekly.
Company began the recall
Added to FDA's Enforcement Report · Classified by FDA
Listed on Recall Canary
In FDA's weekly enforcement report
Summary updated

