Z-0667-2022 Class II Terminated
FDA device recall Z-0667-2022 was initiated by C.R. Bard Inc on Jan 27, 2022 and is designated Class II. Reason for recall: There is a potential to leak from the catheter where it connects to the drain bag The recall status is terminated (terminated Jul 10, 2026). Affected quantity: 1620 units.
Recall Details
- Product Type
- Devices
- Report Date
- Mar 2, 2022
- Initiation Date
- Jan 27, 2022
- Termination Date
- Jul 10, 2026
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 1620 units
Product Description
BARD SURESTEP INTERMITTENT CATHETER TRAY, 14Fr, REF INTS16C
Reason for Recall
There is a potential to leak from the catheter where it connects to the drain bag
Distribution Pattern
US Nationwide distribution in the states of GA, ME, NJ, WI, MN, SD, CO, ND, ID, IL, FL, LA, MD, PA, OH, NE.
Code Information
Serial Number/UDI NGEWX117 (01)00801741183249(17) NGEXX133/(01)00801741183249(17) NGEY0842/(01)00801741183249(17) NGEZ1823/(01)00801741183249(17)
Source
- Dataset
- openFDA device recall enforcement reports
- FDA record
- This recall in openFDA (JSON)
- Enforcement Report
- Search FDA's Enforcement Report for Z-0667-2022
- openFDA file date
- Oct 26, 2026
- Loaded by RegDataLab
- Oct 27, 2026