Recall Z-0759-2025— MEDLINE INDUSTRIES, LP - Northfield

Class II · Ongoing

Class II FDA medical device recall by MEDLINE INDUSTRIES, LP - Northfield, initiated 2024-11-12. FDA's recall record names no specific 510(k) clearance for this event. Product: ST IUD REMOVAL HOOK 10" (504090), Medline Item No. I68785. Reason: 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..

Recalling firm
MEDLINE INDUSTRIES, LP - Northfield
Classification
Class II
Status
Ongoing
Initiated
2024-11-12
Firm location
Northfield, IL, United States

Product description

ST IUD REMOVAL HOOK 10" (504090), Medline Item No. I68785

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.

Data sourced from openFDA. This site is unofficial and independent of the FDA.