Recall Summary
| Recall number | Z-2257-2026 |
| Issued by | U.S. Food and Drug Administration |
| Date | 2026-06-10 |
| Company | Becton Dickinson & Company |
| Units affected | 5,940 |
| 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 Z-2257-2026 affects spinal anesthesia trays used in hospitals and surgery centers. The U.S. Food and Drug Administration announced the action on June 10, 2026. It covers BD Spinal Trays that contain a BD Whitacre needle and injectable anesthetic drugs. The FDA classified this as a Class I recall. That is the agency’s most serious recall category. As a result, patients and healthcare providers should pay close attention. This guide explains what the recall covers, why it happened, and what to do next.
What the Becton Dickinson Recall Covers
The becton dickinson recall covers the BD Spinal Tray with BD Whitacre Needle, 25 G x 3.5 inches. Each tray includes lidocaine HCl 1% in a 5 mL container. It also includes bupivacaine HCl 0.75% with dextrose 8.25% in a 2 mL container, known as Marcaine. The affected catalog numbers are 405637 and 405707. In most cases, these trays are used to deliver spinal anesthesia before surgery or childbirth.
The FDA lists the recall number as Z-2257-2026. The agency dated the action June 10, 2026. The recall covers 5,940 units in total. These trays are medical products sold to healthcare facilities, not directly to consumers. However, patients who recently received spinal anesthesia may still want answers. Typically, the facility that performed the procedure can confirm which products it used.
This becton dickinson recall is a sub-recall of another company’s action. Huons Co., Ltd. manufactures the bupivacaine hydrochloride in dextrose injection included in the trays. Huons recalled that drug first. Becton Dickinson & Company packaged the drug inside its spinal trays. As a result, the trays had to be recalled as well. The tray itself was pulled because of the drug component inside it.
If you work in a healthcare facility, check your inventory now. Look for the two catalog numbers listed above. For example, anesthesia carts, storage rooms, and procedure kits should all be checked. The official recall entry is available in the FDA recall database. That listing is the record of truth for this becton dickinson recall.
The Hazard and Reported Injuries
The hazard behind this becton dickinson recall involves drug quality. The FDA inspected the manufacturing facility of Huons Co., Ltd. During that inspection, the agency identified quality issues. It cited specific quality deficiencies related to acceptance testing. Acceptance testing is how a manufacturer confirms that a drug batch meets its standards. Problems in that process raise doubts about the product’s quality.
The FDA assigned this recall a Class I classification. Under FDA definitions, Class I is the most serious level. It applies when there is a reasonable probability that a product could cause serious health consequences or death. That classification reflects the potential risk, not a confirmed outcome. However, it signals that regulators view the concern as significant. Spinal anesthesia drugs go directly into the space around the spinal cord, so quality matters greatly.
The agency record does not state whether any injuries have been reported. This guide will not speculate either way. Do not assume that harm occurred, and do not assume that it did not. If you experienced unusual symptoms after a spinal procedure, talk to your doctor. Typically, a physician can evaluate whether your symptoms need follow-up care.
| Recall Number | Z-2257-2026 |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Date | June 10, 2026 |
| Company | Becton Dickinson & Company |
| Units Affected | 5,940 |
| Severity | Class I |
The table above summarizes the verified facts from the agency record. Keep these details handy if you contact a facility, the company, or an attorney. For example, the recall number helps staff locate the exact action quickly. Accurate records make every later step easier.
What To Do If You Own This Product
Healthcare facilities should stop using the affected trays immediately. Pull them from anesthesia carts, kits, and storage areas. Quarantine the units so no one uses them by mistake. Then check the catalog number printed on the packaging. The becton dickinson recall applies to catalog numbers 405637 and 405707. If your stock matches, follow your facility’s recall procedures and document each step.
The agency record for this recall does not include usable remedy details on this page. As a result, we will not guess at the return or replacement process. Instead, follow the instructions in the official notice linked on this page. You can find the listing through the FDA enforcement report search. The official notice controls what facilities should do with affected units.
Patients cannot buy these trays at a store, but they can still act. If you had spinal anesthesia in 2026, you may ask your provider about it. For example, ask whether the facility used BD Spinal Trays with the recalled lots. Ask whether the facility received a becton dickinson recall notice. In most cases, hospitals keep records of the products used in each procedure.
Keep your own records too. Save appointment dates, discharge papers, and any symptom notes. Write down who you spoke with and what they said. However, do not panic if you cannot get answers right away. Facilities often need time to review recall notices. Persistent, polite follow-up usually works best.
Does a Becton Dickinson Recall Mean You Can Sue?
A recall is not a lawsuit. This point matters, so we will say it plainly. The becton dickinson recall is a safety action taken with FDA oversight. It removes potentially defective products from use. It does not decide fault, and it does not award money to anyone. No court is involved in the recall itself.
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A recall alone is not a legal claim. To bring a product liability case, a person typically needs an injury. They also need evidence that the product caused that injury. Lawyers call this causation. For example, a patient would need to show they received a recalled tray. They would also need to link their harm to the product’s quality problem. Without both pieces, a claim usually cannot move forward.
If you believe a recalled product harmed you, speak with a licensed attorney. Most product liability lawyers offer free consultations. An attorney can review your medical records and the recall record together. You may be eligible to pursue a claim if the facts support one. However, no outcome is ever guaranteed. Be cautious with anyone who promises a specific result.
Timing also matters. Every state sets deadlines called statutes of limitations. These deadlines limit how long you have to file a claim. In most cases, the clock starts when you knew or should have known about the injury. As a result, waiting too long can end a valid claim before it starts. Early legal advice protects your options.
How Recalls Connect to Mass Tort Cases
Recalls often become important evidence in later litigation. A recall shows that a company or regulator identified a problem. It documents the defect, the dates, and the scope. Plaintiffs’ attorneys use those records to build timelines. For example, they may compare when a company knew of a problem with when it acted. A becton dickinson recall record could serve that same documentary role if litigation ever developed.
History offers clear examples. The Philips CPAP recall of 2021 involved foam that could degrade inside breathing machines. That recall preceded large-scale litigation and an eventual settlement program. The Takata airbag recalls grew into the largest automotive recall in U.S. history. Those recalls anchored years of injury lawsuits. In both cases, the recall itself was the starting document, not the finish line.
To be clear, we have not verified any lawsuit over this specific becton dickinson recall. Do not assume litigation exists just because a recall does. Most recalls never lead to lawsuits. However, recalls involving Class I risks draw more attention than routine ones. If credible litigation develops, consumer-safety resources like this page typically get updated.
Frequently Asked Questions
What products does the becton dickinson recall include?
It covers the BD Spinal Tray with BD Whitacre Needle, 25 G x 3.5 inches, catalog numbers 405637 and 405707. Each tray contains lidocaine 1% and bupivacaine 0.75% with dextrose, known as Marcaine. The FDA recall number is Z-2257-2026.
Why were the spinal trays recalled?
The trays contain a bupivacaine drug made by Huons Co., Ltd., which was recalled first. The FDA found quality deficiencies related to acceptance testing during a facility inspection. As a result, Becton Dickinson recalled the trays containing that drug.
Have injuries been reported in the becton dickinson recall?
The official agency record does not state whether injuries have been reported. Therefore, this guide makes no claim either way. If you had spinal anesthesia recently and feel unwell, contact your doctor and ask your facility about the recall.
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.