Recall Summary
| Recall number | Z-2765-2026 |
| Issued by | U.S. Food and Drug Administration |
| Date | 2026-07-29 |
| Company | Medline Industries, LP |
| Units affected | 318 |
| 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
medline industries recall notices matter to anyone who has had knee or hip surgery recently. On July 29, 2026, the U.S. Food and Drug Administration recorded a Class I recall involving Medline Industries, LP. The action covers MEDLINE medical procedure convenience kits used in orthopedic operating rooms. These kits contained ICU Medical, Inc. pain management kits with Bupivacaine Hydrochloride in Dextrose Injection, USP. Those drug components were recalled over quality issues that could make the medication ineffective. The recall number is Z-2765-2026, and 318 units are affected.
What the Medline Industries Recall Covers
The medline industries recall applies to specific medical procedure convenience kits. These are pre-assembled trays that hospitals open in the operating room. Each kit bundles the supplies a surgical team needs for one procedure. In this case, the kits were built for total knee and hip surgeries.
The FDA record lists several Medline kit SKUs. They include TOTAL KNEE-LF kits with SKUs CDSOPT590T and CDSOPT590U. The record also lists TOTAL KNEE CDS with SKU CDS983930J. Two HIP CDS-LF kits appear as well, under SKUs CDS984556L and CDS984556M. Additional TOTAL KNEE configurations are included in the agency listing.
These kits are not consumer retail products. For example, you will not find them on a pharmacy shelf. Instead, they ship directly to hospitals, surgical centers, and orthopedic facilities. As a result, most patients never see the packaging or the SKU. Your surgical team handles the kit on your behalf.
The scope of this medline industries recall is 318 units. That is a defined and limited quantity. However, each unit represents a surgical procedure. In most cases, hospitals track kit lot numbers in their supply records. That tracking is how facilities identify which procedures used affected inventory.
The Hazard and Reported Injuries
The hazard in this medline industries recall traces back to a drug component. The kits contained ICU Medical pain management kits with Bupivacaine Hydrochloride in Dextrose Injection, USP. Bupivacaine is a local anesthetic. Surgeons and anesthesiologists use it to numb tissue and control pain after joint replacement.
Those bupivacaine components were recalled over quality issues. According to the FDA record, the issues could result in drug ineffectiveness. In plain terms, the medication might not work as intended. For a pain management drug, that gap matters during and after surgery.
The FDA classified this action as Class I. Class I is the agency’s most serious recall category. Typically, it signals a reasonable probability that use of the product could cause serious harm. The classification reflects potential risk, not a confirmed outcome in any specific patient.
The agency record does not state whether injuries have been reported in connection with this recall. Therefore, this guide makes no claim either way. Readers should not assume harm occurred, and should not assume it did not. The official notice is the authoritative source on that question.
| Recall Number | Z-2765-2026 |
|---|---|
| Issuing Agency | U.S. Food and Drug Administration |
| Recall Date | July 29, 2026 |
| Company | Medline Industries, LP |
| Units Affected | 318 units |
| Severity Classification | Class I |
What To Do If You Own This Product
Most readers will not own these kits personally. They are institutional surgical products. However, hospitals, surgery centers, and supply managers may hold affected inventory. If you manage medical supplies, check your stock against the SKUs listed above.
Do not guess at the correct next step. The agency record for this recall contains remedy text that does not match the product. For that reason, this guide does not state what the remedy is. Instead, follow the instructions in the official notice linked on this page.
You can review the FDA listing here: FDA Recall Notice Z-2765-2026
Patients have a different set of steps. If you had a knee or hip replacement recently, contact your surgeon’s office. Ask whether your procedure used an affected Medline convenience kit. Also ask whether your pain control during recovery went as expected. Typically, the hospital can check its supply and procedure records.
Keep your own paperwork organized. Save discharge summaries, surgical reports, and billing statements. For example, an itemized hospital bill may list supply codes. Documentation helps if questions about the medline industries recall come up later. It also helps your care team answer you accurately.
Does a Medline Industries Recall Mean You Can Sue?
A recall is a safety action. It is not a lawsuit. Those two things are often confused, but they are separate. A recall means a company or an agency moved to pull a product from use. It does not decide fault, and it does not create a legal claim on its own.
The existence of a medline industries recall does not, by itself, mean anyone can sue. Legal claims generally require more than a defect notice. In most cases, a person must show an actual injury. They must also show that the specific product caused that injury.
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Causation is often the hardest part. Surgery involves many variables. Pain after joint replacement is common even when everything goes correctly. As a result, connecting a poor outcome to one drug component requires medical evidence. A doctor’s records and expert review typically carry that weight.
If you believe you were harmed, speak with a licensed attorney in your state. An attorney can review your records and explain your options. You may be eligible to pursue a claim, depending on the facts. No one can promise a result, and this guide does not offer legal advice.
How Recalls Connect to Mass Tort Cases
Recalls sometimes become evidence in later litigation. A recall notice documents that a defect was identified. It also records dates, product identifiers, and the nature of the problem. Attorneys often use that record to establish a timeline. However, a recall does not prove that any individual was injured.
History offers real examples. The Philips CPAP recall in 2021 involved foam that could degrade in breathing machines. That recall was followed by consolidated federal litigation. Takata airbag inflators were recalled across many vehicle brands. Those recalls also preceded large-scale legal proceedings. In both situations, the recall came first and the litigation followed separately.
No such connection is claimed here. This guide does not state that any lawsuit exists over the medline industries recall. It reports the agency record and explains general legal concepts. Readers who want case-specific guidance should consult a qualified attorney.
Frequently Asked Questions
What products does the medline industries recall include?
It covers MEDLINE medical procedure convenience kits for knee and hip surgery. Listed SKUs include CDSOPT590T, CDSOPT590U, CDS983930J, CDS984556L, and CDS984556M. Additional TOTAL KNEE configurations appear in the FDA record.
Why were these surgical kits recalled?
The kits contained ICU Medical pain management kits with Bupivacaine Hydrochloride in Dextrose Injection, USP. Those drug components were recalled over quality issues. According to the FDA, the issues could result in drug ineffectiveness.
What does a Class I classification mean?
Class I is the FDA’s most serious recall category. It typically indicates a reasonable probability of serious health consequences from using the product. The classification describes potential risk, not a confirmed injury in any patient.
Have injuries been reported from this recall?
The agency record does not state whether injuries have been reported. For that reason, this guide makes no claim in either direction. Check the official FDA notice for the most current information.
What should I do if my surgery used one of these kits?
Contact your surgeon’s office and ask about your procedure records. Follow the instructions in the official notice linked on this page. If you believe you were harmed, a licensed attorney can review your situation.
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 August 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.