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C.R. Bard Access Systems, Inc

C.R. Bard Access Systems, Inc Recalls

All product recalls associated with C.R. 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 23081–23100 of 25000 recalls

C.R. Bard Access Systems, Inc: Guidewire, 70cm x 1mm, REF 5583705, Sterile, Single Use, ...

Metal guidewires used in Hemodialysis Catheters may have been reverse loaded within the dispenser. Potential exists for the stiff end of the guidewire to be inserted into the patient instead of the flexible end.

FDAAug 10, 2007Nationwide• C.R. Bard Access Systems, Inc

Becton Dickinson and Company: BD Microkeratome K3000 and K4000;Catalog Number: 378660,...

Microkeratome blade may stop oscillating and transverse the eye causing injury to the cornea

FDAAug 9, 2007Nationwide• Becton Dickinson and Company

BD Diagnostic Systems Lee Laboratories: DIFCO Laboratories, FA Streptococcus Group A, 5mL, Catal...

Incorrect result: The product exhibited decreased fluorescence when testing with the homologous control organism.

1...1153 115411551156 1157...1250

Page 1155 of 1250Next

FDA

Aug 8, 2007

Nationwide

• BD Diagnostic Systems Lee Laboratories

E Light (Plan 9) – fire hazard (2007)

Fire/Burn Risk

The E Light is a 12-Volt DC light fixture with recessed LEDs typically mounted on the ceiling or under a counter. The recalled light is a flat, white rectangle with three LEDs (in the three-watt model) or six LEDs (in the six-watt model).

CPSCAug 3, 2007Nationwide• Plan 9 Inc., of White Salmon, Wash.

Rehvac Relief Plug (Rehvac Manufacturing) – injury risk (2007)

This recall involves the 3000-PSI safety plugs used in the cylinders of Nitrous Oxide systems and in HVAC pressure testing tools. The Nitrous Oxide systems are used as gas boosters for motor vehicles. The plugs are nickel-plated. The number "3000" is stamped on the face of the plug.

CPSCAug 3, 2007Nationwide• Rehvac Manufacturing Co., of San Antonio, Texas

Hi-Heat Aerosol Coating (Sherwin-Williams) – explosion risk (2007)

The recall involves Thermo-Tec Hi-Heat aerosol coating used to color and protect Thermo-Tec automotive exhaust wrap. The part number (#12002) is printed above the UPC, and the date code (#B1815) is written on the bottom of the can. The 11-ounce aerosol can is mostly blue with orange and yellow flames and has an aluminum-colored cap. The can states "HI-HEAT COATING 2000°F" in large white letters on the front of the can.

CPSCAug 3, 2007Nationwide• The Sherwin-Williams Co., of Cleveland, Ohio

Naviscan PET Systems: PEMView Software used with Naviscan PEM Flex Solo I and P...

Naviscan has identified a potential safety issue with all versions of PEM View Software commonly used for analyzing patient images acquired on the PEMFIex product line. 1. The Positron Emission Mammography Standardized Uptake Value (PEMSUV) and distance measurements for the product mentioned above may be inaccurate if a zoomed image has been opened, measurement tools are used, and the applet rema

FDAAug 1, 2007Nationwide• Naviscan PET Systems

Newport Medical Instruments Inc: Newport HT50 Ventilator (all Models)

Battery Life: With use over time, the internal battery begins losing its ability to hold a charge resulting in shortened ventilator operation time. Specifically, Newport has received a number of reports concerning the internal battery not lasting as long as expected followed by ventilator shut down with less advance warning than when the battery was new.

FDAJul 31, 2007Nationwide• Newport Medical Instruments Inc

Hitachi Medical Systems America Inc: Altaire Shoulder Coil, an accessory to the Altaire MRI sy...

Overheating; A portion (balun assembly) of the cable that connects the shoulder coil to the actual MRI unit may malfunction and result in overheating of the balun assembly. The overheating of the balun assembly could result in injury to the patient or operator if either came into contact with the assembly.

FDAJul 30, 2007Nationwide• Hitachi Medical Systems America Inc

B. Braun Medical, Inc.: Normal Saline 3ml in 12ml Syringe. The product is shipped...

Particulate matter in product.

FDAJul 30, 2007Nationwide• B. Braun Medical, Inc.

B. Braun Medical, Inc.: Normal Saline 10ml in 12ml Syringe. The product is shippe...

Particulate matter in product.

FDAJul 30, 2007Nationwide• B. Braun Medical, Inc.

NxStage Medical, Inc.: NxStage Cartridge Express, CAR-170, for hemodialysis.

Potential for dialysate leaks from the cartridge during treatment.

FDAJul 27, 2007Nationwide• NxStage Medical, Inc.

SmartScan Fire Alarm Panel (Gamewell-FCI) – software upgrade (2007)

Fire/Burn Risk

The software upgrade involves the Gamewell-FCI model 600 Series control panel using System Sensor compatible line cards, SmartScan. These panels are components of the Gamewell-FCI 600 Series fire alarm system. They provide the signaling line circuits and display information for the system.

CPSCJul 27, 2007Nationwide• Gamewell-FCI, of Northford, Conn.

Toro Power Sweep Blower (Toro) – projectile hazard (2007)

The recall involves Toro Power Sweep electric blower model 51586 that was manufactured between 2000 and 2002. The electric blowers have serial numbers that range between 000055100 and 220255609. There are two decals on the main housing of the blower. One decal reads, "TORO Power Sweep" and the decal on the opposite side of the blower contains the model number and serial number. The recalled units can be identified by a black impeller fan, which can be seen through the air inlet screen on the bottom of the unit.

CPSCJul 26, 2007Nationwide• The Toro Company, of Bloomington, Minn.

Datex Ohmeda, Inc: GE Disposable Multi Absorber Canister used with EZchange ...

Elevated inspired CO2 levels related to the use of the Datex-Ohmeda GE Healthcare Disposable Multi Absorber Canister with the EZchange Module.

FDAJul 24, 2007Nationwide• Datex Ohmeda, Inc

Philips Medical Systems North America Co. Phillips: Philips Multi Diagnost Eleva

Units do not comply with the requirement to provide automatic beam limitation within +/- 3 degrees of horizontal, vertical, and perpendicular to the plane of the image receptor during radiographic procedures.

FDAJul 23, 2007Nationwide• Philips Medical Systems North America Co. Phillips

Philips Medical Systems North America Co. Phillips: Philips Digital Diagnost X-Ray system

FDAJul 23, 2007Nationwide• Philips Medical Systems North America Co. Phillips

Philips Medical Systems North America Co. Phillips: Philips Easy Diagnost Eleva

FDAJul 23, 2007Nationwide• Philips Medical Systems North America Co. Phillips

Philips Medical Systems North America Co. Phillips: Philips Bucky DIagnost X-Ray System

FDAJul 23, 2007Nationwide• Philips Medical Systems North America Co. Phillips

Philips Medical Systems North America Co. Phillips: Philips Easy Diagnost X-Ray System

FDAJul 23, 2007Nationwide• Philips Medical Systems North America Co. Phillips