Bard Access Systems Recalls Groshong NXT ClearVue Catheters Due to Connector Defects
Bard Access Systems is recalling specific lots of Groshong NXT ClearVue Catheters because connector defects may prevent proper catheter passage or locking.
What this means for you
Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.
Our severity reasoning: The recall involves a medical device with functional defects that could prevent proper use or locking, representing a risk of harm where specific injury reports are not detailed in the source text.
Plain-English summary
Bard Access Systems Inc. is recalling specific lots of REF 69655405 Groshong NXT ClearVue Catheters with Sherlock Tip Location System (TLS) Stylet, Basic Kit, 4F, Single-Lumen. The affected lots are redx4687, rees1313, and reev1270. These medical devices are designed for use when central venous catheterization is prescribed.
The recall is due to two manufacturing issues: the inner diameter of the distal connector may be reduced, resulting in the inability to pass the catheter through the connector, or the catch slot on the distal connector may be deformed, resulting in the inability to properly lock the device.
The affected products were distributed worldwide, including nationwide in the United States and in various international markets. Healthcare providers and facilities should identify and stop using the affected lots. Patients who have received these devices should contact their healthcare provider for guidance.
The recalled product
- Product
- REF 69655405, Groshong NXT ClearVue Catheter with Sherlock Tip Location System (TLS) Stylet, Basic Kit, 4F, Single-Lumen, TLS, UDI: (01)10801741147521 - Product Usage: is designed for use when central venous catheterization is prescribed.
- Manufacturer
- Bard Access Systems Inc.
- Category
- Medical Device — Catheters
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (3)
- Lot No. redx4687
- rees1313
- reev1270
Distribution
Part of a larger recall action
This product is one of 18 recalled by Bard Access Systems Inc. under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
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