FDA Enforcement
Class II
Terminated
NEEDLEMASTER 4MMx 25G LOWER, model no. NM-610U-0425 - Product Usage: Used with endoscopes to perform endoscopic vascular or submucosal injection in the GI tract.
Recall: Z-1043-2021
·
Reported February 17, 2021
Enforcement
- Recall Number
- Z-1043-2021
- Event ID
- 87074
- Classification
- Class II
- Status
- Terminated
- Product Type
- Devices
- Firm
- Aomori Olympus Co., Ltd.
- Voluntary / Mandated
- Voluntary: Firm initiated
- Initial Notification
- Letter
- Report Date
- February 17, 2021
- Initiation Date
- January 4, 2021
- Classification Date
- February 5, 2021
- Termination Date
- March 11, 2024
- Address
- 2 Chome 248-1, Okkonoki, Kuroishi, N/A, N/A, Japan
Description
NEEDLEMASTER 4MMx 25G LOWER, model no. NM-610U-0425 - Product Usage: Used with endoscopes to perform endoscopic vascular or submucosal injection in the GI tract.
Reason
Inspection confirmed a small percentage of sterile packages with inadequate package seal (partial heat seal). Patients may develop infections if non-sterile equipment is used.
Code Info
01K, 02K, 03K, 04K, 05K, 06K, 07K, 08K, 09K, 0XK, 98K, 99K, 9XK, 9YK, 9ZK, 05V, 06V, 07V, 09V, 0XV
Distribution
US Nationwide distribution.
Quantity
7,400,000 (globally); 260,395 (US)