Medline Industries, LP recalls SCISSORS
- Recalling company
- Medline Industries, LP
- Product
- SCISSORS, OR, SHARP/BLUNT, 5.5", STERILE, Item Number DYND04000
- Reason
- The items may have weak packaging seals that may result in a breach of sterility if the seal fails and may lead to an increased risk of infection if product is utilized.
- Classification
- Class II – may cause temporary or medically reversible health consequences
- Recall date
- Nov 13, 2025
- Reported
- Dec 24, 2025
- Distribution
- US Nationwide distribution in the states CA, CO, IL, KS, and MI.
- Status
- Ongoing
- Quantity
- 56 units
- Lot / codes
- DYND04000, UDI-DI: 10193489191349(each), 20193489191346(case), Lot Number: 2023102590
- Company location
- Northfield, IL
- Recall type
- Voluntary: Firm initiated
- Recall number
- Z-0921-2026
- Agency
- U.S. Food and Drug Administration (FDA)
View official FDA notice ↗ Search recall number Z-0921-2026 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.