Recall Summary
| Recall number | Z-3151-2026 |
| Issued by | U.S. Food and Drug Administration |
| Date | 2026-09-23 |
| Company | AVID Medical, Inc. |
| Units affected | 1,640 |
| 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
Avid medical recall Z-3151-2026 affects a hospital epidural kit made by AVID Medical, Inc. The U.S. Food and Drug Administration posted the recall on September 23, 2026. It covers 1,640 units of the Haylard 18G Single Shot Epi Tray. The FDA rated it Class I, its most serious category. The concern involves sodium chloride ampules inside the kits. Spectra Medical has recalled those ampules separately. If you or someone you love had an epidural, this guide explains what the recall means.
What the Avid Medical Recall Covers
This recall covers one product. It is the Haylard 18G Single Shot Epi Tray. The kit’s model or item number is DPGE002-02. Anyone checking their supplies should match that number exactly. The agency data summarized here does not list specific lot codes. As a result, facilities should check the official FDA notice for lot details.
An epidural tray is a pre-packed procedure kit. Clinicians typically use it to give a single-shot epidural injection. These trays often bundle needles, syringes, drapes, and solutions together. For example, a kit may include sodium chloride for flushing or for checking needle position. The “18G” label refers to the needle gauge.
AVID Medical assembles procedure trays for healthcare providers. In most cases, kits like this go to hospitals, surgery centers, and clinics. They are not usually sold to the public in stores. However, patients can still be affected if a recalled kit is used during their care. That is why the avid medical recall matters to providers and patients alike.
The data summarized here does not give exact distribution dates or regions. The FDA date of record is September 23, 2026. If you need distribution details, read the official FDA notice. That notice is the most reliable source for scope and timing. Any details you find elsewhere should match it.
The Hazard and Reported Injuries
The avid medical recall stems from a problem with a component. According to the FDA, the concern is product quality and sterility. The kits contain sodium chloride ampules that Spectra Medical has recalled. Because the ampules are packed inside the trays, the finished kits are affected too. This is often called a downstream or component recall.
Sterility matters a great deal in epidural procedures. The needle enters a space close to the spinal cord. Typically, any contamination risk in that area is taken very seriously. In general, non-sterile items used near the spine can raise infection concerns. However, the agency record does not describe contamination actually found in these kits.
The FDA classified this avid medical recall as Class I. Under FDA definitions, Class I is the highest risk level. It means use of the product could cause serious health consequences or death. It does not mean harm has already happened. Instead, it reflects the potential risk the agency identified.
The agency record does not say whether any injuries have been reported. We do not know either way. Readers should not assume harm occurred. They also should not assume it did not. If you have health concerns, talk with your doctor. The table below summarizes the verified recall data.
| Detail | Information |
|---|---|
| Recall number | Z-3151-2026 |
| Agency | U.S. Food and Drug Administration |
| Date | September 23, 2026 |
| Company | AVID Medical, Inc. |
| Product | Haylard 18G Single Shot Epi Tray (Item DPGE002-02) |
| Units affected | 1,640 |
| Severity | Class I |
What To Do If You Own This Product
Most readers will not own this product directly. It is a clinical kit used by trained staff. However, hospitals, surgery centers, and pain clinics may have it in stock. Staff handling the avid medical recall should check supply rooms for item number DPGE002-02. Any matching kits should be set aside and not used.
The remedy text in the agency record did not match this product. As a result, we have not included it here. Please follow the instructions in the official notice instead. You can find it in the FDA device recall database. For questions about next steps, contact AVID Medical or your supplier.
Patients have different steps to consider. If you had a single-shot epidural recently, you may wonder about your kit. In most cases, you cannot know without asking. You can contact the facility where you were treated. Ask whether they used kits named in the avid medical recall.
Watch for any unusual symptoms after a procedure. General warning signs can include fever, worsening back pain, or redness at the injection site. If something concerns you, seek medical care promptly. You can also report problems to the FDA through its MedWatch program. Those reports help the agency track device safety.
Keep good records if you think you were affected. Save discharge papers, procedure notes, and bills. Write down dates and the names of facilities. Typically, these records help doctors understand your history. They can also help if you later speak with a lawyer.
Does an Avid Medical Recall Mean You Can Sue?
A recall is not a lawsuit. It is a safety action. A company removes or corrects a product, often with FDA oversight. The avid medical recall is a regulatory step meant to reduce risk. It is not a court finding of fault or liability.
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A recall alone does not create a legal claim. Typically, a claim requires an actual injury. It also requires proof that the product caused that injury. For example, a patient may need medical records linking an infection to a recalled kit. Without injury and causation, there is usually no case.
We have not verified any lawsuit tied to this recall as of this writing. That could change over time. However, no one should assume litigation will follow. Many recalls never lead to lawsuits at all. Others lead to only a few individual claims.
If you believe you were harmed, speak with a licensed attorney. Many product liability lawyers offer free consultations. An attorney can review your records and explain your options. Depending on the facts, you may be eligible to pursue a claim. However, no outcome is guaranteed. Filing deadlines also apply, so timing matters.
How Recalls Connect to Mass Tort Cases
Recalls sometimes become evidence in later litigation. For example, Philips recalled millions of CPAP and ventilator devices in June 2021. The concern involved sound-abatement foam that could break down. Lawsuits followed and were consolidated in federal court in Pennsylvania. The recall record became an important part of those cases.
Takata airbags offer another example. Defective inflators led to the largest auto recall in U.S. history. Injured drivers and passengers filed many lawsuits. Those cases were grouped into multidistrict litigation in Florida. In both examples, the recall helped document a defect. However, each plaintiff still had to prove their own injuries.
Recall files can include company letters, FDA classifications, and inspection findings. Lawyers sometimes use these records to show what a company knew and when. As a result, recall documents can shape how a case develops. Still, a recall record is only one piece of evidence.
It is too early to know whether the avid medical recall will follow a similar path. In most cases, component recalls involve narrow product lines. Litigation depends on reported harm, evidence, and many other factors. We will update this page if verified developments occur.
Frequently Asked Questions
What product is part of the avid medical recall?
The recall covers the Haylard 18G Single Shot Epi Tray, item number DPGE002-02. The FDA lists 1,640 affected units. The recall number is Z-3151-2026.
Why did the FDA classify this as a Class I recall?
The kits contain sodium chloride ampules that Spectra Medical recalled. The FDA cited possible product quality and sterility issues. Class I is the agency’s most serious risk category, though it does not confirm that harm occurred.
Can I file a lawsuit because of the avid medical recall?
A recall by itself is not a lawsuit or a legal claim. You would typically need an injury that is linked to the product. A licensed attorney can review your situation, but no outcome is guaranteed.
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 September 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.