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.