PlainRecalls
FDA Devices Moderate Class II Ongoing

ST OR MAYO HEGAR NEEDLEHOLDER 6"(OR2500), Medline Item No. 67870

Reported: January 1, 2025 Initiated: November 12, 2024 #Z-0756-2025

Product Description

ST OR MAYO HEGAR NEEDLEHOLDER 6"(OR2500), Medline Item No. 67870

Reason for Recall

Weak seals may result in a breach of sterility, which may not be detectable to the user. This can lead to increased risk of contamination and infection.

Details

Units Affected
21,440 total
Distribution
US Nationwide distribution.
Location
Northfield, IL

Frequently Asked Questions

What product was recalled?
ST OR MAYO HEGAR NEEDLEHOLDER 6"(OR2500), Medline Item No. 67870. Recalled by MEDLINE INDUSTRIES, LP - Northfield. Units affected: 21,440 total.
Why was this product recalled?
Weak seals may result in a breach of sterility, which may not be detectable to the user. This can lead to increased risk of contamination and infection.
Which agency issued this recall?
This recall was issued by the FDA Devices on January 1, 2025. Severity: Moderate. Recall number: Z-0756-2025.