HIGH

Medline Recalls Adhesive Bandages Over Sterility Concerns

Medline Industries recalled 1,725,600 units of Quick Strip Plastic Sterile Adhesive Bandages due to potential packaging defects. The recall, issued on October 27, 2025, affects all lots of Curad Touch-Free and Quick-Strip Bandages. Open seals may compromise the sterility of the product, posing a health risk.

Quick Facts at a Glance

Recall Date
October 27, 2025
Hazard Level
HIGH
Brand
Medline Industries, LP
Category
Health & Personal Care
Sold At
Multiple Retailers
At-Risk Groups
GENERAL

Hazard Information

Medline has identified that all lots of the Curad Touch-Free and Quick-Strip Bandages may exhibit open seals in the packaging which may compromise the sterility of the product.

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: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

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 recalled product is Quick Strip Plastic Sterile Adhesive Bandages, measuring 0.75 inches by 3 inches. The Medline item number is NON25500QS. These bandages were distributed throughout the US, Guam, Canada, and the United Arab Emirates.

The Hazard

The open seals in the packaging may compromise the sterility of the bandages, which can lead to infections or other complications. This recall is classified as Class II, indicating a potential for serious health risks.

Reported Incidents

As of now, there are no reported incidents or injuries related to the use of these bandages. However, the potential for compromised sterility presents a significant health risk.

What to Do

Patients and healthcare providers should stop using these bandages immediately. Contact Medline Industries or your healthcare provider for further instructions on how to proceed.

Contact Information

For more details, call Medline at 1-800-633-5463 or visit their website at www.medline.com. Additional recall information is available on the FDA website.

Key Facts

  • Recall date: October 27, 2025
  • Quantity: 1,725,600 units
  • Distribution: US, Guam, Canada, UAE
  • Class II recall due to sterility risk
  • Stop using affected bandages immediately

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
UDI/DI 10888277699397 (each)
20888277699394 (box)
30888277699391 (case)
ALL LOTS
Report Date
December 17, 2025
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