Medline Industries, LP recalls MEDLINE PERFUSION SYRINGE
- Recalling company
- Medline Industries, LP
- Product
- MEDLINE PERFUSION SYRINGE, REF: DYNJ39223C
- Reason
- Medline Industries, LP is issuing a recall for specific item(s) and lot(s) of Medline Kits containing BD Luer Tip Caps. BD has issued a recall of their Luer Tip Caps after confirming through internal testing that certain BD Luer Tip Cap trays failed routine biocompatibility testing. Although the tip cap covers a small surface area of the syringe and does not come in direct contact with patients, there is the potential that the failure of a biocompatibility test may have varying consequences ranging from no harm or clinical impact to potential for sensitization, irritation, pyrogenicity, acute systemic toxicity or hemolysis depending on the nature and duration of contact with the syringe.
- Classification
- Class II – may cause temporary or medically reversible health consequences
- Recall date
- Oct 27, 2025
- Reported
- Dec 17, 2025
- Distribution
- US Nationwide distribution in the state of CA.
- Status
- Ongoing
- Quantity
- 15 units
- Lot / codes
- UDI/DI 10193489621532 (each) 40193489621533 (case), Lot Number 25FMJ081
- Company location
- Northfield, IL
- Recall type
- Voluntary: Firm initiated
- Recall number
- Z-0886-2026
- Agency
- U.S. Food and Drug Administration (FDA)
View official FDA notice ↗ Search recall number Z-0886-2026 in the FDA Enforcement Report. Also see FDA recall press releases.
If you use this product, check the lot, NDC or model number against the official notice and follow its instructions. Do not stop a prescribed medicine or remove a medical device without talking to your doctor or pharmacist. Report problems to FDA MedWatch. FoodRecallNow summarizes public FDA data and is not medical advice.