Z-0921-2026 Class II Ongoing
FDA device recall Z-0921-2026 was initiated by Medline Industries, LP on November 13, 2025 and is designated Class II. 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. The recall status is ongoing. Affected quantity: 56 units.
Recall Details
- Product Type
- Devices
- Report Date
- December 24, 2025
- Initiation Date
- November 13, 2025
- Termination Date
- N/A
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 56 units
Product Description
SCISSORS, OR, SHARP/BLUNT, 5.5", STERILE, Item Number DYND04000
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.
Distribution Pattern
US Nationwide distribution in the states CA, CO, IL, KS, and MI.
Code Information
DYND04000, UDI-DI: 10193489191349(each), 20193489191346(case), Lot Number: 2023102590