BD¿Spinal Tray with BD¿Quincke Needle 26 G x 3.5 in.; Recall: What To Do

becton dickinson recall notices matter to anyone who has had a spinal procedure. On June 10, 2026, the U.S. Food and Drug Administration listed a Class I recall of the BD Spinal Tray with BD Quincke Needle. The tray includes lidocaine and bupivacaine with dextrose.

The recall was issued by Becton Dickinson & Company. It is a sub-recall tied to a problem at the drug manufacturer. Class I is the FDA’s most serious category. If you or a family member had a spinal injection recently, this guide explains what is known.

What the Becton Dickinson Recall Covers

The recalled item is a prepackaged spinal anesthesia tray. Its full description is the BD Spinal Tray with BD Quincke Needle 26 G x 3.5 in. The tray contains lidocaine HCL (1%), 5 mL. It also contains bupivacaine HCL (0.75%) with dextrose (8.25%), 2 mL, sold under the name marcaine. The catalog number is 405632.

The becton dickinson recall carries FDA recall number Z-2250-2026. The recall date on the agency record is June 10, 2026. The scope covers 890 units. That is a relatively small number of trays. However, a small unit count does not lower the severity rating. Each tray is used in a clinical procedure on a patient.

This is not a consumer retail product. For example, you will not find a spinal tray on a pharmacy shelf. These trays are sold to hospitals, surgical centers, and clinics. As a result, most patients never see the packaging or the catalog number. Typically, the tray is opened by clinical staff in a procedure room. Patients learn about a becton dickinson recall only through their provider or through news coverage.

The becton dickinson recall is a sub-recall. The original recall came from Huons Co, Ltd. Huons is the manufacturer of the Bupivacaine Hydrochloride in Dextrose Injection, USP. Becton Dickinson packaged that drug into its own tray kit. When the upstream drug was recalled, the finished tray was pulled as well. In most cases, that is how sub-recalls work.

The Hazard and Reported Injuries

The hazard here is a manufacturing quality problem. The FDA inspected the Huons manufacturing facility. During that inspection, the agency cited specific quality deficiencies. Those deficiencies related to acceptance testing. Acceptance testing is how a manufacturer confirms a batch meets its own specifications before release.

When acceptance testing is deficient, a company cannot fully confirm product quality. That is the core concern in this becton dickinson recall. The agency record does not describe a specific defect found in any individual tray. Instead, it describes a breakdown in the testing process. However, regulators treat that gap seriously for injectable drugs used near the spine.

The FDA classified this becton dickinson recall as Class I. Class I is reserved for situations where use of the product may cause serious health consequences or death. That classification reflects risk, not a confirmed outcome. The agency record does not state whether any injuries have been reported. We will not claim injuries occurred, and we will not claim none occurred.

Here are the verified details from the agency record in one place.

What To Do If You Own This Product

Most readers will not personally own this product. It is a professional medical device kit. However, some clinics, mobile surgical providers, and pain management practices do hold inventory. If your facility stocks spinal trays, check your shelves now. Look for catalog number 405632 on the tray label or carton.

If you find matching trays, stop using them. Set them aside from active inventory. For example, place them in a clearly marked quarantine bin. That prevents accidental use during a busy procedure day. Typically, facilities also notify their materials management or risk management team at this stage.

We are not stating what the remedy is for this becton dickinson recall. The remedy text in the agency record does not match the product described, so we have withheld it. Follow the instructions in the official notice instead. You can read it here: FDA Enforcement Report — official recall notice

Patients have a different set of steps. If you had a spinal or epidural procedure recently, ask your provider directly. Ask whether your facility used catalog number 405632. Ask whether any of the recalled lots were on hand. As a result of the becton dickinson recall, many facilities have already reviewed their records. Report any new or unusual symptoms to your doctor without delay.

Does a Becton Dickinson Recall Mean You Can Sue?

A recall is not a lawsuit. That is the single most important point in this section. A recall is a safety action. A company removes or corrects a product, often working with a regulator. It is a forward-looking fix, not a finding of legal fault.

As a result, a becton dickinson recall by itself is not a legal claim. No court has ruled on this recall. We have not verified that any lawsuit exists over recall Z-2250-2026. We are not stating that one does. Do not assume a recall notice means money is available to anyone.

A personal injury claim generally needs more than a recall notice. In most cases, a plaintiff must show a real injury. They must also show that the specific product caused that injury. That link is called causation. Causation is often the hardest part of a medical product case, and it usually requires medical records and expert review.

If you believe you were harmed, talk to a licensed attorney in your state. An attorney can review your records and explain your options. You may be eligible to bring a claim, depending on the facts. However, no one can guarantee an outcome, and no one can promise compensation. Deadlines called statutes of limitations also apply, so do not wait indefinitely.

How Recalls Connect to Mass Tort Cases

Recalls sometimes become evidence in later litigation. A recall notice can show what a company knew and when it knew it. Inspection findings can show whether quality systems were working. Typically, plaintiffs’ lawyers request these documents in discovery. However, evidence of a defect is still not the same as proof that one patient was harmed.

Real examples show the pattern. Philips recalled millions of CPAP and BiPAP machines in 2021 over foam degradation. That recall was followed by consolidated federal litigation. Takata airbag inflators were recalled across many automakers, and that recall also preceded large-scale litigation and a bankruptcy. For example, in both situations the recall came first and the court cases followed later, over a period of years.

Not every recall follows that path. Most recalls end quietly with corrected products and no litigation at all. The becton dickinson recall discussed here is a quality-system recall of a small number of units. As a result, it may never lead to any case. We will update this page if the verified public record changes.

Frequently Asked Questions

What product is covered by this becton dickinson recall?

The recall covers the BD Spinal Tray with BD Quincke Needle 26 G x 3.5 in., catalog number 405632. The tray contains lidocaine HCL (1%) and bupivacaine HCL (0.75%) with dextrose (8.25%). The FDA recall number is Z-2250-2026.

Why was this becton dickinson recall issued?

It is a sub-recall of a recall by Huons Co, Ltd., which manufactures the bupivacaine in dextrose injection. The FDA inspected the Huons facility and cited quality deficiencies related to acceptance testing. Becton Dickinson pulled the finished trays that contained that drug.

Have injuries been reported from this recall?

The FDA record for this recall does not state whether injuries have been reported. We will not claim that injuries occurred, and we will not claim that none did. If you had a spinal procedure and feel unwell, contact your doctor.

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.

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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.