Z-3071-2024 Class II Ongoing
FDA device recall Z-3071-2024 was initiated by MEDLINE INDUSTRIES, LP - Northfield on June 18, 2024 and is designated Class II. Reason for recall: A non-sterile Mastisol component, which was not labeled as being sterile or non-sterile, was placed in the non-sterile portion of certain sterile convenience kits and distributed. In the event that t… The recall status is ongoing. Affected quantity: 105 units.
Recall Details
- Product Type
- Devices
- Report Date
- September 18, 2024
- Initiation Date
- June 18, 2024
- Termination Date
- N/A
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 105 units
Product Description
ANESTHESIA TURNOVER KIT, Pack Number DYNJAA0377
Reason for Recall
A non-sterile Mastisol component, which was not labeled as being sterile or non-sterile, was placed in the non-sterile portion of certain sterile convenience kits and distributed. In the event that the user assumes sterility during its use, there is an increased risk of patient infection.
Distribution Pattern
US: TX, IL, CA
Code Information
UDI/DI Case 40195327231126, UDI/DI Each 10195327231125; Lot Numbers: 22LBM357