FDA Medical devices recall ·
ST REPROCESSED BRUNS CURETTE #00 (BC00), Medline Item No recall
- Recall number
- Z-0758-2025
- Date
- (initiated November 12, 2024)
- Company / brand
- Medline Industries, LP
3 Lakes Dr, Northfield, IL, United States - Category
- Medical devices › Class II
- Classification
- Class II
- Status
- Ongoing
- Units affected
- 21,440 total
- Hazard tags
- Sterility Microbial contamination
- Initiated by
- Voluntary: Firm initiated
Read the official FDA notice ↗
Product
ST REPROCESSED BRUNS CURETTE #00 (BC00), Medline Item No. 67600K
Why was it 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.
What should you do?
FDA enforcement reports do not list a consumer remedy. Check the product codes below against what you have; if it matches, stop using it and follow the instructions in the firm's or FDA's official notice, or contact the company. If you have health concerns, contact your healthcare provider.
Product codes & lot numbers
UDI: 10653160382140 (ea) 00653160382143 (case); Lot 2023012490
Distribution
US Nationwide distribution.
What does Class II mean?
Class II means use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or the probability of serious harm is remote.
Source: FDA (medical devices), recall Z-0758-2025. Official notice. Republished from public data; RecallFlag is not affiliated with the FDA.