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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 1181–1200 of 25000 recalls

PowerPICC Catheters (Bard) – tubing specification issue (2025)

Catheters indicated for short-or-long term access to the central venous system have tubing that exceeded melt flow index specification (higher), which could lead to increased material fatigue leaks, which could lead to infiltration, extravasation, discomfort, phlebitis, bleeding, air embolism, foreign body embolism, infection and interruption to therapy.

High

FDAMar 11, 2025Nationwide• Bard Access Systems, Inc.

ChlorproMAZINE Tablets 100mg (Glenmark) – CGMP Deviations (2025)

CGMP deviations: presence of N-Nitroso-Desmethyl Chlorpromazine impurity above the recommended interim limit.

Class IIModerate

FDAMar 11, 2025Nationwide• Glenmark Pharmaceuticals Inc., USA

Philips DXR System (Philips) – collimator fall risk (2025)

Potential for collimator to fall as a result of incorrect installation.

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Moderate

FDAMar 10, 2025Nationwide• Philips North America Llc

Omni-Macs Dietary Supplement (Veridance) – Excessive Iodine (2025)

Levels of iodine exceeding label claim

Class IIModerate

FDAMar 10, 2025IN, MO• Veridance Pharmacal, LLC

TLX/TLC Implant Driver (Straumann) – depth marking missing (2025)

The devices are missing the laser marked depth markings.

Low

FDAMar 8, 2025Nationwide• Straumann USA LLC

Cinacalcet Hydrochloride Tablets (Slate Run Pharmaceuticals) – Nitrosamine Impurity (2025)

CGMP deviations: The presence of nitrosamine impurity above the acceptable daily intake limits.

Class IIModerate

FDAMar 7, 2025Nationwide• Slate Run Pharmaceuticals

Cinacalcet Hydrochloride Tablets (Slate Run Pharmaceuticals) – Nitrosamine Impurity (2025)

CGMP deviations: The presence of nitrosamine impurity above the acceptable daily intake limits.

Class IIModerate

FDAMar 7, 2025Nationwide• Slate Run Pharmaceuticals

Sodium Bicarbonate Injection (Exela Pharma) – Sterility Concern (2025)

Lack of Assurance of Sterility

Class IIModerate

FDAMar 7, 2025Nationwide• Exela Pharma Sciences LLC

Venue Go Models R2/R3 (GE Medical Systems) – Battery Fire Risk (2025)

Fire/Burn Risk

The battery for certain ultrasound systems can potentially develop an internal failure which could result in smoke or fire.

High

FDAMar 6, 2025Nationwide• GE Medical Systems, LLC

Phosphate Reagent Bottles (Taylor Water Technologies) – test kit risk (2025)

Fire/Burn Risk

This recall involves the replacement reagent #1 bottles sold with Taylor Phosphate Test Kits #K-1106 and also sold separately. The kits are used to test the level of phosphate in water for pools, spas and aquariums. The water testing kits are labeled with the brand name "Taylor," the kit name "Phosphate Test" and part number "K-1106." The bottle in the kit that contains sulfuric acid is labeled with the brand name "Taylor," product name "Phosphate Reagent #1," part number "R-0980" and "A Size: 22 mL (.75 oz)." The replacement reagent bottle that is sold separately has the same label. Phosphate Reagent #1 has a shelf-life of 24 months.

High

CPSCMar 6, 2025Nationwide• Taylor Water Technologies LLC, of Sparks, Maryland

Fentanyl Citrate (QuVa Pharma) – Sterility Concern (2025)

Lack of Assurance of Sterility

Class IIModerate

FDAMar 6, 2025Nationwide• QuVa Pharma, Inc.

Fentanyl Citrate (QuVa Pharma) – Sterility Concern (2025)

Lack of Assurance of Sterility

Class IIModerate

FDAMar 6, 2025Nationwide• QuVa Pharma, Inc.

Fentanyl Citrate (QuVa Pharma) – Sterility Concern (2025)

Lack of Assurance of Sterility

Class IIModerate

FDAMar 6, 2025Nationwide• QuVa Pharma, Inc.

Venue Fit Models R3/R4 (GE Medical Systems) – Battery Fire Risk (2025)

Fire/Burn Risk

The battery for certain ultrasound systems can potentially develop an internal failure which could result in smoke or fire.

High

FDAMar 6, 2025Nationwide• GE Medical Systems, LLC

Airstream Classic (Airstream) – Electrical System Fault (2025)

Fire/Burn Risk

Airstream, Inc. (Airstream) is recalling certain 2021-2025 Airstream Classic 33', 2024-2025 Classic 30', and 2025 Classic 28' travel trailers. The sofa footrest switch may have underrated wiring, which can allow the wiring to overheat.

High

NHTSAMar 5, 2025Nationwide• AIRSTREAM

Blueprint Mixed Reality (Stryker) – Guidance Instrumentation Difficulties (2025)

Stryker identified an elevated complaint rate related to difficulties using the Blueprint Mixed Reality Guidance Instrumentation system is multifactorial, but in each instance prohibits the system from meeting its intended use. The most commonly reported complaints were related to impaired software functioning, impaired instrumentation functioning, and general difficulties using the product.

Moderate

FDAMar 5, 2025AK, ID, MA +4 more• Tornier S.A.S. 161 Rue Lavoisier Montbonnot-Saint-Martin France