Medline Industries, LP: Device Recall
Recall #Z-0921-2026 · 11/13/2025
Class II: Risk
Recall Details
- Recall Number
- Z-0921-2026
- Classification
- Class II
- Product Type
- Device
- Recalling Firm
- Medline Industries, LP
- Status
- Ongoing
- Date Initiated
- 11/13/2025
- Location
- Northfield, IL, United States
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 56 units
Reason for Recall
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.
Product Description
SCISSORS, OR, SHARP/BLUNT, 5.5", STERILE, Item Number DYND04000
Distribution Pattern
US Nationwide distribution in the states CA, CO, IL, KS, and MI.
Other Recalls by Medline Industries, LP
- Class II: Risk 12/16/2025
- Class II: Risk 12/16/2025
- Class II: Risk 12/16/2025
- Class II: Risk 12/16/2025
- Class II: Risk 12/16/2025
Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.