Z-2024-2024 Class II Ongoing
FDA device recall Z-2024-2024 was initiated by MEDLINE INDUSTRIES, LP - Northfield on Apr 30, 2024 and is designated Class II. Reason for recall: There is the potential of the tip protector to fall off 4.5" sterile, curved, Iris Scissors The recall status is ongoing. Affected quantity: 67811 units.
Recall Details
- Product Type
- Devices
- Report Date
- Jun 12, 2024
- Initiation Date
- Apr 30, 2024
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 67811 units
Product Description
MEDLINE STERILE IRIS SCISSORS CVD/STD REF DYNJ04049 (case) and DYNJ04049H (individual unit)
Reason for Recall
There is the potential of the tip protector to fall off 4.5" sterile, curved, Iris Scissors
Distribution Pattern
Worldwide distribution - US Nationwide and the countries of Singapore, Canada.
Code Information
UDI/DI 10080196847273, Lot Numbers: 23GBV681, 23HBD138, 23IBF254, 23LBJ787
Source
- Dataset
- openFDA device recall enforcement reports
- FDA record
- This recall in openFDA (JSON)
- Enforcement Report
- Search FDA's Enforcement Report for Z-2024-2024
- openFDA file date
- Oct 23, 2026
- Loaded by RegDataLab
- Oct 25, 2026