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Bard Access Systems, Inc

Bard Access Systems, Inc Recalls

All product recalls associated with Bard Access Systems, Inc.

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Recall Summary

Total Recalls

1000

Past Year

1000

Class I (Serious)

127

Most Recent

Jan 2026

Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.

Showing 24141–24160 of 25000 recalls

Bard Access Systems, Inc: Intraoperative Ultrasound Cover Kit

Conductivity gel pouches, labeled as sterile, and packaged in various kits may not be sterile.

FDANov 3, 2004Nationwide• Bard Access Systems, Inc

Access CardioSystems: AccessAED Package (with audio record) Model Number: 9100...

Device may fail to deliver shock due to a faulty circuit board

FDANov 3, 2004Nationwide• Access CardioSystems

Access CardioSystems: AccessAED PAD Package (without ECG trace) Model Number: ...

Device may fail to deliver shock due to a faulty circuit board

FDANov 3, 2004Nationwide• Access CardioSystems

1...1206 120712081209 1210...1250

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Bard Access Systems, Inc: Site-Rite Sterile Needle Guide Kit - 18 gauge

Conductivity gel pouches, labeled as sterile, and packaged in various needle guide kits may not be sterile.

FDANov 3, 2004Nationwide• Bard Access Systems, Inc

Salsa Campeon Bicycle Forks (Quality Bicycle Products) – Carbon Fiber Defect (2004)

The recall involves carbon fiber/aluminum forks included with the Salsa model F-01 Campeon frame set in either White/Black or Red/Black color combinations. Units included in this recall have a code of CK, DA, or DB and a serial number from 03400 to 04600. The model number, date code and serial number are located on a label at the base of the steerer tube near the crown of the fork.

CPSCNov 2, 2004Nationwide• Quality Bicycle Products, Inc., of Bloomington, Minn.

Robertshaw TS-11 Gas Valve (Robertshaw) – Commercial Equipment Risk (2004)

Fire/Burn Risk

The TS-11 Thermal Safety Control Gas Valves are installed in commercial cooking equipment with pilot lights, including ranges, griddles, fryers, and warming trays. The recalled gas valves were produced between February 2003 and August 2004. The "magnet heads" on the gas valves were made during the same range of dates. The recalled products can be identified by date codes 0306 through and including 0432. The TS-11 gas valve with different manufacturing dates and a different hazard was recalled in 2002.

CPSCNov 1, 2004Nationwide• Robertshaw Controls Company of Long Beach, California

Cardinal Health 1430 Waukegan Rd Attn V. Mueller Qa McGaw Park IL 60085: V. Mueller Pfister-Schwartz Stone Retriever 4-Wire Basket...

The dispenser box was mislabeled with the wrong length and the wrong wire gauge.

FDAOct 27, 2004MS, MO, NY +4 more• Cardinal Health 1430 Waukegan Rd Attn V. Mueller Qa McGaw Park IL 60085

Gaymar Industries Inc: XPRT Therapy Mattress Systems: Model # 2950-000-000 with...

Design control/validation deficiencies.

FDAOct 25, 2004HI, IN, NE• Gaymar Industries Inc

Polaris RANGER 4x4 Utility Vehicle (Polaris) – Vehicle Safety Concern (2004)

All model year 2005 "RANGER 4x4" Utility Vehicles with model number R05RD50AA are part of this recall. The model number is located on the upper right frame tube directly under the right side of the seat. The RANGER 4x4 Utility Vehicles have black seats with a green chassis. "RANGER 4x4" is prominently displayed on the right and left side of the rear cargo box.

CPSCOct 21, 2004Nationwide• Polaris Industries, Inc., of Medina, Minn.

ela Medical Llc: Alto implantable cardioverter defibrillator

Alto Implantable Defibrillators Models 614 and 615. These models can experience sudden no output, and early end of life characteristics due to metal migration in their controlling hybrids, causing high current drain leading to premature battery depletion.

FDAOct 21, 2004Nationwide• ela Medical Llc

General Electric Med Systems LLC: Patient tables of CT systems with brand name: CT/e; CT/e ...

The patient tables of the affected CT systems are supported by a hydraulic cylinder and a cylinder shaft (i.e. the upper shaft) which connects the tabletop to the table frame. GE received a report of a HiSpeed LX/I system table falling abruptly due to the filure of the upper shaft. No injuries were reported.

FDAOct 21, 2004Nationwide• General Electric Med Systems LLC