Quick Facts at a Glance
- Recall Date
- January 7, 2026
- Hazard Level
- HIGH
- Brand
- Medline Industries, LP
- Category
- Health & Personal Care
- Sold At
- Multiple Retailers
- Geographic Scope
- 1 states
- At-Risk Groups
- GENERAL
What to Do Now
Use this page like a recall checklist: verify the product first, then act on the official remedy.
Immediate steps
- 1Stop using the product until you confirm whether it is included in the recall.
- 2Compare the product label, model number, UPC, color, size, and purchase location against the identifiers below.
- 3Follow the official remedy from FDA - Medical Devices; save photos, receipts, labels, and correspondence before contacting the company.
- 4If the product could harm a child, older adult, pet, or patient, move it out of reach immediately.
Check these identifiers
- Brand
- Medline Industries, LP
- Product type
- Nerve Block Kit
- Model numbers
- 1) PAIN0150C, UDI-DI: 10193489819571(each), 21JBV886(case), Lot Number: 21JBV886
- Sold at
- Multiple Retailers
- Where affected
- ALL
Recall Timeline
Key dates and source checks for this recall record.
Recall announced
January 7, 2026
Reported by FDA DEVICE
February 25, 2026
RecallRadar source check
March 4, 2026
Consumer action
Use the official remedy and keep documentation.
Hazard Information
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packaging cycles; however, the identified calibration issues have the potential to impact the sterility assurance level (SAL) of the Recalled Products.
What You Should Do
Patients and healthcare providers should stop using this device immediately. Follow the recall instructions provided by the manufacturer. Contact Medline Industries, LP or your healthcare provider for instructions. Notification method: Letter
About This Product
The BASIC NERVE BLOCK TRAY W/LINEN is used in medical procedures to deliver anesthetic near nerves. Healthcare providers typically use this kit during surgeries or pain management treatments.
Why This Is Dangerous
Calibration issues with sterilization equipment may lead to inadequate sterilization, increasing the risk of infections for patients undergoing procedures that utilize this kit.
Industry Context
This recall is not part of a broader industry pattern.
Real-World Impact
Patients and healthcare providers face potential health risks if the product is used. The urgency of the recall may lead to disruptions in medical procedures that rely on this nerve block kit.
Practical Guidance
How to identify if yours is affected
- Check the model number PAIN0150C on the device packaging or documentation.
- Verify the lot number 21JBV886 to see if your product is affected.
- Review any correspondence from Medline regarding this recall.
Where to find product info
The model number and lot number can typically be found on the packaging or the device itself.
What timeline to expect
Expect a refund processing timeline of approximately 4-6 weeks after returning the product.
If the manufacturer is unresponsive
- Document all communication attempts with Medline.
- Consider escalating the issue to the FDA if no response is received.
How to prevent similar issues
- Always check for recalls on medical devices before use.
- Ensure medical suppliers provide devices that meet current safety standards.
- Ask about the sterilization processes used for medical devices.
Documentation advice
Keep records of your product purchase, any correspondence with the manufacturer, and documentation of the recall notice.
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Product Details
The recall involves the BASIC NERVE BLOCK TRAY W/LINEN, Model Number PAIN0150C. The recalled units were distributed worldwide, including the U.S. The products were sold as part of Medline's convenience kits.
Key Facts
- Recall date: January 7, 2026
- Class II recall
- Potential sterility assurance level issues
- Affected model: PAIN0150C
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Safety Guide
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