BARD SURESTEP INTERMITTENT CATHETER TRAY, 14Fr, REF INTS14C
Reported: March 2, 2022 Initiated: January 27, 2022 #Z-0666-2022
Product Description
BARD SURESTEP INTERMITTENT CATHETER TRAY, 14Fr, REF INTS14C
Reason for Recall
There is a potential to leak from the catheter where it connects to the drain bag
Details
- Recalling Firm
- C.R. Bard Inc
- Units Affected
- 2120 units
- Distribution
- US Nationwide distribution in the states of GA, ME, NJ, WI, MN, SD, CO, ND, ID, IL, FL, LA, MD, PA, OH, NE.
- Location
- Covington, GA
Frequently Asked Questions
What product was recalled? ▼
BARD SURESTEP INTERMITTENT CATHETER TRAY, 14Fr, REF INTS14C. Recalled by C.R. Bard Inc. Units affected: 2120 units.
Why was this product recalled? ▼
There is a potential to leak from the catheter where it connects to the drain bag
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on March 2, 2022. Severity: Moderate. Recall number: Z-0666-2022.
Related Recalls
FDA Devices Moderate
Convenience Kits 1. 25GA Convenience Kit - FNX VS0644.25-FNX 2. 25GA Convenience Kit - FXX VS0644.25-FXX 3.2…
Vortex Surgical Inc. · 2026-02-11
FDA Devices Moderate
COULTER DxH Diluent, REF 628017 COULTER DxH ECO Diluent REF C67250 For use as an isotonic buffered diluent in conju…
Beckman Coulter, Inc. · 2026-02-11
FDA Devices Moderate
Product Name: Single Use 3-Lumen Sphincterotome V Model/Catalog Number: KD-V411M-1520 Product Description: These inst…
Olympus Corporation of the Americas · 2026-02-11
FDA Devices Moderate
Product Name: Disposable Triple Lumen Sphincterotome Model/Catalog Number: KD-401Q-0330 Product Description: These in…
Olympus Corporation of the Americas · 2026-02-11
FDA Devices Moderate
Product Name: Lumipulse pTau 217 Plasma Controls Model/Catalog Number: 81558 Software Version: Not Applicable Produc…
Fujirebio Diagnostics, Inc. · 2026-02-11