Bard recalls Groshong NXT ClearVue Catheter 4 Fr Single-Lumen due to lidocaine ampoules being manufactured under deficient practices. Affected units have UDI-DI code 00801741035258 and lot number REKY1686.
Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.
Bard is recalling Groshong NXT ClearVue Catheter 4 Fr Single-Lumen units because lidocaine ampoules used in their production were made with deficient manufacturing practices. This could lead to improper medication delivery if the ampoules are used.
Lidocaine ampoules are critical for medication delivery during IV therapy. If manufactured under deficient practices, these ampoules could contain impurities or be improperly labeled, leading to incorrect medication administration.
Healthcare professionals who use the Groshong NXT PICC catheters for intravenous therapy or blood sampling may be affected. Patients receiving treatment with these catheters are at risk if the lidocaine ampoules are used incorrectly.
Check for the UDI-DI code 00801741035258 and lot number REKY1686 on the catheter packaging. The product is sold under the brand name Groshong NXT ClearVue Catheter 4 Fr Single-Lumen.
Look for the UDI-DI code 00801741035258 and lot number REKY1686 on the catheter packaging.
The lidocaine ampoules used in manufacturing were produced under deficient practices, which could lead to improper medication delivery.
Check the UDI-DI code and lot number on the packaging. If it matches 00801741035258 and REKY1686, contact Bard for further instructions.
The recall is due to manufacturing deficiencies in lidocaine ampoules, but the official notice does not specify if this poses a risk of serious injury.
We’ve drafted a message you can send Bard to request your refund or repair — edit it as you like.
Subject: Recall Z-2665-2026 — Bard Bard Hello, I own a Bard that is covered by recall Z-2665-2026 from Bard. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
