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Medline Recalls Nerve Block Tray Over Sterility Concerns

Medline Industries recalled 448 units of its BASIC NERVE BLOCK TRAY W/LINEN on January 7, 2026. The recall stems from calibration issues with sterilization equipment that may affect the product's sterility assurance level. Healthcare providers should stop using the device immediately and follow the provided instructions.

Official notice
Medline Industries, LPHealth & Personal CareMedical Devices1) PAIN0150CUDI-DI: 10193489819571(each)21JBV886(case)

Source-backed recall notice

No product image was available from the source feed.

Official source
FDA DEVICE
Recall date
January 7, 2026
Status
ACTIVE
Severity
8/10

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

  1. 1Stop using the product until you confirm whether it is included in the recall.
  2. 2Compare the product label, model number, UPC, color, size, and purchase location against the identifiers below.
  3. 3Follow the official remedy from FDA - Medical Devices; save photos, receipts, labels, and correspondence before contacting the company.
  4. 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.

  1. Recall announced

    January 7, 2026

  2. Reported by FDA DEVICE

    February 25, 2026

  3. RecallRadar source check

    March 4, 2026

  4. 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

  1. Check the model number PAIN0150C on the device packaging or documentation.
  2. Verify the lot number 21JBV886 to see if your product is affected.
  3. 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

Safety Guide

Not sure what to do next? Our guide walks you through the process step by step.

Read: What to Do When You Find a Recalled Product

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Safety Assessment

Risk LevelHIGH
Severity Score
8/ 10
Affected Groups
GENERAL
Injury Types
OTHER

Product Classification

Product Details

Model Numbers
1) PAIN0150C
UDI-DI: 10193489819571(each)
21JBV886(case)
Lot Number: 21JBV886
Affected States
ALL
Report Date
February 25, 2026
Recall Status
ACTIVE

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