Every recall we track for Bard Access Systems, Inc. — 38 in all — plus the complaints and injury reports the public filed about them.
Bard recalls specific needle kits for powered drivers due to risk of obturator locking to needle hub, potentially causing delayed therapy during emergency IV access.
Bard Access Systems recalls specific Power-Trialysis dialysis catheters due to lidocaine ampoules manufactured under deficient practices. Affected units have UDI-DI codes and lot numbers listed. Consumers should check their catheter details and contact Bard for guidance.
Bard recalls specific PowerPICC catheter models due to lidocaine ampoules manufactured under deficient practices. Affected units have UDI-DI codes and lot numbers listed. Contact Bard for details.
Bard Access Systems recalls two soft tissue biopsy trays due to lidocaine ampoules being manufactured under deficient practices. These trays may pose a risk if used with affected ampoules.
Bard recalls PowerMidline Catheter 4 Fr Dual-Lumen models with specific UDI-DI codes due to lidocaine ampoules manufactured under deficient practices. Affected units may pose risks from improper manufacturing.
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.
Bard recalls THORA/PARA trays with lidocaine ampoules made under deficient practices. Affected units have specific UDI-DI codes and lot numbers. Stop using immediately to avoid potential injury.
Bard Access Systems recalls PowerPICC SOLO HF Catheter 5 Fr Triple-Lumen with UDI-DI Code 00801741129674 due to lidocaine ampoules manufactured under deficient practices. Affected units may pose risks from improper manufacturing.
Bard recalls specific PowerPICC SV catheter models due to lidocaine ampoules being manufactured under deficient practices. Affected units have unique UDI-DI codes and lot numbers. Consumers should check their catheters for these identifiers.
Bard Access Systems recalls PowerPICC Provena catheters due to lidocaine ampoules being manufactured under deficient practices. Check your UDI-DI codes and lot numbers for affected models.
Bard recalls 5625240 DuoGlide Short-Term Straight Dialysis Catheters due to lidocaine ampoules being manufactured under deficient practices. Affected units have UDI-DI code 00801741042119 and lot number REKY0255.
Bard recalls specific Provena Midline Catheters due to lidocaine ampoules manufactured under deficient practices. Affected units have UDI-DI codes and lot numbers listed. Consumers should check their catheters against the provided details.
Bard recalls PowerMidline Catheter models with specific UDI-DI codes due to lidocaine ampoules being manufactured under deficient practices. Affected units may pose risks if used improperly.
Bard recalls specific Power-Trialysis Slim-Cath dialysis catheters due to lidocaine ampoules manufactured under deficient practices. Affected units have UDI-DI codes starting with 00801741107177. No remedy is stated in the recall notice.
Bard recalls specific poly midline catheters due to lidocaine ampoules made under deficient manufacturing practices. Affected units have UDI-DI codes 00801741121609 and 00801741108051. Contact Bard for details.
Bard Access Systems recalls 4Fr Single-Lumen PowerPICC Catheters with tubing that may leak, causing discomfort, infection, or other complications. Affected units have specific reference codes and expiration dates.
Bard Access Systems recalls Intraosseous needle kits with potential for needle assembly loss during use. Affected models include D015151NK, D015151MK, and others. Stop using immediately to prevent injury.
Bard Access Systems recalls 5Fr PowerPICC Catheter kits with incorrect micro-introducers. This could lead to improper catheter placement risks during procedures.
Bard recalls 5 Fr IR PowerPIC: 50cm guidewire in kits labeled for 70cm. This mismatch may cause complications during procedures. Affected units have specific labels and lot numbers.
Bard Access Systems recalls Groshong NXT ClearVue Catheter kits due to potential distal connector issues that may prevent proper catheter insertion or locking.
Bard Access Systems recalls replacement connectors for 4F Groshong NXT clearVue PICC catheters due to potential fit problems that may prevent proper catheter insertion or locking.
Bard recalls Groshong NXT ClearVue Catheter with Sherlock 3CG Tip Positioning System due to potential distal connector issues that may prevent proper catheter insertion or locking.
Bard Access Systems recalls Groshong NXT ClearVue Catheter Basic Kits due to potential connector issues that may prevent catheter passage or proper locking. Affected kits have specific UDI codes and lot numbers listed in the recall.
Bard Access Systems recalls Groshong NXT ClearVue Catheter with Sherlock 3CG Tip Positioning System due to distal connector problems that may prevent catheter insertion or proper locking.
Bard Access Systems recalls Groshong NXT ClearVue Catheter kits due to potential connector issues that may prevent catheter passage or proper locking. Affected units have specific UDI codes and lot numbers.
Bard Access Systems recalls Groshong NXT ClearVue Catheter with Sherlock Tip Location System due to distal connector problems that may prevent catheter insertion or proper locking.
Bard Access Systems recalls Groshong NXT ClearVue Catheter with Sherlock Tip Location System due to distal connector problems that may prevent proper catheter insertion and locking.
Bard Access Systems recalls Groshong NXT ClearVue Catheter kits due to potential connector issues that may prevent catheter passage or proper locking. Affected units have specific UDI codes and lot numbers.
Bard recalls Groshong NXT ClearVue Catheter with potential distal connector problems that may prevent proper catheter insertion or locking. Affected units have specific model numbers and lot codes.
Bard Access Systems recalls Groshong NXT ClearVue Catheter with Sherlock Tip Location System due to distal connector issues that may prevent proper catheter insertion or locking.
Bard Access Systems recalls Groshong NXT ClearVue Catheter with Sherlock Tip Location System due to distal connector problems that may prevent proper catheter insertion or locking.
Bard Access Systems recalls Groshong NXT ClearVue Catheter Basic Kit due to distal connector problems that may prevent proper catheter insertion or locking.
Bard recalls Groshong NXT ClearVue Catheter kits with potential connector issues that could prevent catheter passage or secure locking. Affected units have specific lot numbers and UDI codes.
Bard recalls Groshong NXT ClearVue Catheter with Sherlock Tip Location System due to distal connector problems that may prevent catheter insertion or locking. Affected units have specific model and lot numbers.
Bard recalls Groshong NXT ClearVue Catheter with Sherlock Tip Location System due to distal connector problems that may prevent catheter passage or proper locking. Affected units have specific UDI codes and lot numbers.
Bard Access Systems recalls Groshong NXT ClearVue Catheter kits due to distal connector problems that may prevent proper catheter insertion or locking. Affected units have specific UDI and lot numbers.
Bard Access Systems recalls Groshong NXT ClearVue Catheter intermediate kits due to connector problems that may prevent catheter insertion. Affected units have specific UDI codes and lot numbers.
Bard Access Systems recalls PowerPICC Provena Catheters (3 Fr. Single lumen and 4 Fr. Dual Lumen) due to possible leaks at the luer hub extension leg junction. Product codes and serial numbers listed in the recall.
