Recall Summary
| Recall number | Z-2251-2026 |
| Issued by | U.S. Food and Drug Administration |
| Date | 2026-06-10 |
| Company | Becton Dickinson & Company |
| Units affected | 330 |
| Severity | Class I |
Remedy: Follow the instructions in the official notice linked below. The agency record for this recall did not contain remedy text we could verify against this product, so we have not reproduced it here.
Read the official U.S. Food and Drug Administration recall notice
becton dickinson recall notices matter to anyone who has spent time in a hospital or surgical center. On June 10, 2026, the U.S. Food and Drug Administration recorded a Class I recall involving Becton Dickinson & Company. The affected product is a spinal anesthesia tray sold to medical facilities. It is not a consumer retail item. However, patients who received spinal anesthesia may still want to understand what happened.
What the Becton Dickinson Recall Covers
The becton dickinson recall covers the BD Spinal Tray with BD Whitacre Needle, 22 G x 3.5 in. Each tray contains lidocaine HCL (1%), 5 mL. It also contains bupivacaine HCL (0.75%) with dextrose (8.25%), 2 mL, commonly known as marcaine. The catalog number is 405645. That catalog number is the single clearest way to identify the product.
The FDA assigned this action recall number Z-2251-2026. The agency listed the scope as 330 units. That is a small number by recall standards. However, a Class I designation means the FDA considers the risk serious. For example, Class I is the agency’s highest severity tier for recalled products.
This is a sub-recall. The underlying issue originated with Huons Co., Ltd. Huons manufactured the Bupivacaine Hydrochloride in Dextrose Injection, USP, that was packaged inside the trays. Becton Dickinson assembled the finished kit. As a result, the recall flows downstream from a component supplier to the tray itself.
Spinal trays like this one are distributed to hospitals, ambulatory surgery centers, and clinics. They are not sold in pharmacies to the public. In most cases, the people handling this product are anesthesiologists, nurse anesthetists, and hospital supply staff. Typically, a facility’s materials management team is the group that must locate and quarantine affected units.
The Hazard and Reported Injuries
The becton dickinson recall stems from quality issues found during an FDA inspection of a manufacturing facility. The FDA cited specific quality deficiencies related to acceptance testing. Acceptance testing is how a manufacturer confirms that a drug batch meets its own specifications before release. When that testing is deficient, the manufacturer cannot fully verify what is in the vial.
This matters because bupivacaine is injected into the spinal space. Anesthetic drugs delivered near the spinal cord leave no margin for uncertainty. However, the agency record does not describe a specific defect found in any individual tray. It describes a breakdown in the testing process that is supposed to catch problems.
The agency record does not state whether any injuries have been reported in connection with this becton dickinson recall. We will not claim that injuries occurred. We also will not claim that none occurred. Readers should rely on the official FDA notice for any updates on that question.
| Recall number | Z-2251-2026 |
| Issuing agency | U.S. Food and Drug Administration |
| Recall date | June 10, 2026 |
| Company | Becton Dickinson & Company |
| Product | BD Spinal Tray with BD Whitacre Needle 22 G x 3.5 in., Catalog Number 405645 |
| Units affected | 330 |
| Severity classification | Class I |
A Class I classification reflects potential severity, not confirmed harm. Typically, the FDA uses it when there is a reasonable probability that a product could cause serious injury or death. That is a forward-looking risk assessment. It is not a finding that anyone was hurt.
What To Do If You Own This Product
If your facility stocks this product, stop using it immediately. Check your inventory for catalog number 405645. Pull any matching BD Spinal Trays with the 22 G x 3.5 in. Whitacre needle from active supply. Quarantine them somewhere clinical staff cannot reach them by mistake.
Next, follow the instructions in the official FDA notice linked on this page. The correction or removal instructions for this becton dickinson recall come from the manufacturer and the agency. We are not stating what the remedy is here. Facilities should read the notice directly and follow it exactly.
Contact Becton Dickinson customer service if your records are unclear. Hospital risk management and materials management should be looped in early. For example, many facilities log recall actions for accreditation purposes. Documenting what you found and what you did is worth the time.
If you are a patient rather than a provider, you cannot check this yourself. You do not have access to the catalog numbers used in your procedure. However, you can request your anesthesia records from the facility. In most cases, those records identify the specific products and lot numbers used during your care.
Does a Becton Dickinson Recall Mean You Can Sue?
No. A recall is a safety action, not a lawsuit. This is worth stating plainly, because the two are often confused. The becton dickinson recall is a regulatory event. It means a product was pulled from the market. It does not mean a court has found anyone liable for anything.
📨 Get Free Mass Tort Guides Alerts
Free · No spam · Unsubscribe anytime
A recall by itself is not a legal claim. Typically, a personal injury claim requires more than a defective product. It generally requires an actual injury, and evidence linking that injury to the product. Lawyers call that second piece causation. Without both elements, a recall notice alone does not create a case.
We are not aware of any verified lawsuit filed over this specific becton dickinson recall. We are not stating that one exists. If you believe you were harmed after a spinal anesthesia procedure, you may be eligible to pursue a claim. Whether you actually are depends on facts a lawyer would need to review.
Speak with a licensed attorney in your state if you have concerns. Bring your medical records, your procedure dates, and the facility name. No article can tell you whether you have a case. There are no guarantees of compensation, and anyone who promises one is not being straight with you.
How Recalls Connect to Mass Tort Cases
Recalls sometimes become evidence in later litigation. A recall notice can establish when a company learned of a problem. It can also document what the company told regulators and when. As a result, plaintiffs’ attorneys often treat recall records as an early timeline anchor. However, the notice itself proves nothing about any individual patient’s injury.
Real examples show how this plays out. The Philips CPAP recall in 2021 involved sound-abatement foam that could degrade. Thousands of individual claims were later consolidated into multidistrict litigation. The Takata airbag inflator recalls followed a similar path over many years. In both situations, the recall came first and the litigation developed afterward, based on documented injuries. A becton dickinson recall would not automatically follow that pattern. Most recalls never produce litigation at all.
Frequently Asked Questions
What product is covered by this Becton Dickinson recall?
The recall covers the BD Spinal Tray with BD Whitacre Needle, 22 G x 3.5 in., catalog number 405645. Each tray contains lidocaine HCL (1%) and bupivacaine HCL (0.75%) with dextrose (8.25%). The FDA listed 330 units in the recall scope.
Why was this becton dickinson recall issued?
It is a sub-recall tied to Huons Co., Ltd., the maker of the bupivacaine component. The FDA identified quality deficiencies related to acceptance testing during a facility inspection. The recall addresses that manufacturing quality problem.
Have injuries been reported in this becton dickinson recall?
The agency record does not state whether injuries have been reported. We will not claim either way. Check the official FDA notice linked on this page for the most current information.
Were You Injured by a Recalled Product?
A recall by itself is a safety action, not a legal claim. However, if a recalled product caused a real injury, you may be eligible to pursue compensation. A licensed attorney can review your situation at no upfront cost — most work on contingency, meaning you pay nothing unless you recover.
Official Sources & Resources
Verify every recall against the issuing agency before acting:
- U.S. Food and Drug Administration: official recall database — the record of truth for this notice
- CPSC: cpsc.gov — household goods, toys, furniture, appliances
- FDA: fda.gov — food, drugs, and medical devices
- NHTSA: nhtsa.gov — vehicles, tires, and child car seats
- USDA FSIS: fsis.usda.gov — meat, poultry, and egg products
Content last reviewed July 2026. This is general educational information, not legal advice. If you notice outdated information, please contact us.
Related Guides
- All Product Recalls
- All Active MDL Cases
- Mass Tort Explainers
- Mass Tort Tips
- Tort Reform by State — 50-State Comparison
Attorney Advertising. The information on this page is provided for general informational purposes only and does not constitute legal advice. A product recall is a safety action by a manufacturer or regulator and does not by itself establish liability or create a legal claim. No attorney-client relationship is created by accessing or using this content. Every case is unique. If you believe you were harmed by a recalled product, consult a licensed attorney in your jurisdiction.