HIGH

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.

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

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

Get instant alerts for Health & Personal Care recalls

Be the first to know. Free instant alerts to your inbox.

No spamUnsubscribe anytime

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.

The Hazard

Calibration issues with the sterilization equipment raise concerns about the sterility of the devices. This defect increases the risk of infection or other complications for patients receiving nerve block procedures.

Reported Incidents

No specific incidents or injuries have been reported in connection with this recall. The potential for infection due to compromised sterility warrants immediate action.

What to Do

Stop using the BASIC NERVE BLOCK TRAY W/LINEN immediately. Contact Medline Industries at the provided recall instructions. Follow directions from your healthcare provider regarding usage.

Contact Information

For further assistance, reach out to Medline Industries, LP. Visit their website or call customer service for more details.

Key Facts

  • Recall date: January 7, 2026
  • 448 units recalled
  • Class II recall
  • Potential sterility assurance level issues
  • Affected model: PAIN0150C

Get Alerts for Health & Personal Care Recalls

Get instant alerts for recalls that affect you. Free forever.

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

Related Recalls

HIGH

Fresenius Kabi Vancomycin Injection Recalled Over Sterility Concerns

Fresenius Kabi Compounding recalled its vancomycin HCl injection on February 5, 2026, due to a lack of assurance of sterility. This Class II recall affects all lots distributed nationwide. Healthcare providers and consumers must stop using the product immediately.

Fresenius Kabi Compounding
Lack of
Read more
HIGH

Fresenius Kabi Compounding Issues Recall of Vancomycin Injection

Fresenius Kabi Compounding recalled 1,578 bags of vancomycin HCl injection on February 5, 2026. The company cited a lack of assurance of sterility as the reason for the recall. Healthcare providers and consumers should stop using the product immediately.

Fresenius Kabi Compounding
Lack of
Read more
HIGH

Pro Numb Tattoo Numbing Spray Recalled Due to cGMP Violations

Pro Numb Tattoo Numbing Spray was recalled on February 2, 2026 due to cGMP deviations. The product, containing 4% lidocaine, is distributed by Pro Numb Tattoo Numbing Spray LLC. Consumers should stop using it immediately and contact the company for further guidance.

PRO NUMB SENSITIVE SKIN
cGMP deviations
Read more