FDA Enforcement
Class II
Terminated
¿regard SHOULDER ARTHROSCOPY, OR00049Q, Item Number 880044017; ortho surgery convenience kit
Recall: Z-0305-2023
·
Reported November 30, 2022
Enforcement
- Recall Number
- Z-0305-2023
- Event ID
- 91069
- Classification
- Class II
- Status
- Terminated
- Product Type
- Devices
- Firm
- ROi CPS LLC
- Voluntary / Mandated
- Voluntary: Firm initiated
- Initial Notification
- Report Date
- November 30, 2022
- Initiation Date
- October 20, 2022
- Classification Date
- November 23, 2022
- Termination Date
- April 1, 2026
- Address
- 3000 E Sawyer Rd, N/A, Republic, MO, 65738-2758, United States
Description
¿regard SHOULDER ARTHROSCOPY, OR00049Q, Item Number 880044017; ortho surgery convenience kit
Reason
Surgical convenience kits were distributed containing 3M surgical drapes which were subsequently recalled.
Code Info
UDI/DI 10194717113478, Lot Numbers: 91163, exp 1/10/2024; 91669, exp 2/25/2024; 92537, exp 5/15/2024
Distribution
LA, MO, NC, FL
Quantity
456 kits