FDA Medical devices recall ·
Medline Adult Anesthesia Set recall
- Recall number
- Z-0137-2026
- Date
- (initiated September 10, 2025)
- Company / brand
- Medline Industries, LP
3 Lakes Dr, Northfield, IL, United States - Category
- Medical devices › Class II
- Classification
- Class II
- Status
- Ongoing
- Units affected
- 950 units
- Initiated by
- Voluntary: Firm initiated
Read the official FDA notice ↗
Product
Medline Adult Anesthesia Set, REF DYNJ39985G
Why was it recalled?
Specific items and lots of Medline Kits may contain Clearlink IV Sets which Baxter recalled due to customer reports of leaking.
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/DI 10198459062353 (EA) 40198459062354 (Case), Lot Numbers: 25GMB464
Distribution
US Nationwide distribution in the states of MO.
States: Missouri
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-0137-2026. Official notice. Republished from public data; RecallFlag is not affiliated with the FDA.