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Bard Peripheral Vascular Inc 1625 W 3rd St Bldg 1 850 W. Rio Salado Prkwy. Tempe AZ 85281-2438

Bard Peripheral Vascular Inc 1625 W 3rd St Bldg 1 850 W. Rio Salado Prkwy. Tempe AZ 85281-2438 Recalls

All product recalls associated with Bard Peripheral Vascular Inc 1625 W 3rd St Bldg 1 850 W. Rio Salado Prkwy. Tempe AZ 85281-2438.

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Recall Summary

Total Recalls

1000

Past Year

169

Class I (Serious)

125

Most Recent

Dec 2025

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 161–180 of 1553 recalls

Rotarex Atherectomy System (Bard) – catheter breakage (2025)

Atherectomy Catheter eIFU updated to clarify and emphasize procedural steps intended to reduce the likelihood of catheter breakage events. Catheter has an outer cylinder connected to a rotating helix, which could fracture and/or break, which would require retrieval, and helix facture/break could cause vessel injury and lead to severe bleeding.

FDAFeb 5, 2025Nationwide• Bard Peripheral Vascular Inc 1625 W 3rd St Bldg 1 850 W. Rio Salado Prkwy. Tempe AZ 85281-2438

Beverage Base Lemonade (OCBW) – Undeclared Yellow #5 (2025)

Undeclared Allergen

Undeclared Yellow #5

Class IIModerate

FDAJan 31, 2025AR, CA, CO +5 more• OCBW INC

Beverage Base Sweet&Sour (OCBW) – Undeclared Yellow #5 (2025)

Undeclared Allergen

1...7 8910 11...78

Page 9 of 78Next

Undeclared Yellow #5

Class IIModerate

FDAJan 31, 2025AR, CA, CO +5 more• OCBW INC

Refillable Medicine Bottles (Cabinet Health) – Child-Resistance Failure (2025)

This recall involves certain Cabinet Health 4 oz. Refillable Medicine Bottles with ABS plastic lids. The bottles are made of clear glass with blue, turquoise, orange or purple plastic lids labeled \"CABINET.\" Cabinet Health sold the bottles filled with over-the-counter drugs or as empty 4 oz. bottles. The recalled empty 4 oz. bottles were sold via cabinethealth.com from March 2023 through July 2024. Consumers with recalled empty bottles can identify them by the date of purchase. The recalled bottles filled with over-the-counter drugs have the following date codes on a sticker on the bottom of the bottle. Medication Name Lid Color Date Codes Tension Headache - Refillable Glass Bottle (Acetaminophen 500mg Caffeine 65mg) - 100 Count Blue 2029J07223 2029J07623 2029J07723 Allergy Relief - Refillable Glass Bottle (Diphenhydramine HCl 25mg) - 120 Count Turquoise 2265J07323 Pain Reliever and Nighttime Sleep Aid - Refillable Glass Bottle (Acetaminophen 500mg, Diphenhydramine 25mg) - 120 Count Blue 2127J06823 2127J23323 3040J23323 3051J23323 3051J23423Pain Reliever and Fever Reducer - Refillable Glass Bottle (Acetaminophen 500mg) - 120 Count Blue 2286J06323 2286J06523 2286J06623 2287J06623 2287J06723 Cough Relief - Refillable Glass Bottle (Dextromethorphan Hbr 15mg) - 60 Count Orange 2010J06923 2010J07023 3004J29623 3010J29623 3025J29623 Sleep Aid - Refillable Glass Bottle (Diphenhydramine HCl 50mg) - 70 Count Purple 3021J06823 3021J06923 3034J23423 3034J23523

CPSCJan 30, 2025Nationwide• Cabinet Health Inc., of Washington, D.C.

Infant Learning Toy Sets (Pearhead) – Choking Risk (2025)

Choking Hazard

This recall involves Pearhead Learning Sets with model number 87150. The Learning Sets are sold in a box with the words "learning set developmental toys for babies 0-6 months." The eight-piece Learning Sets include a cow stroller toy, crinkle sheep toy, black and white tummy time book with flashcards, plush activity cube and a wooden egg shaker rattle. The model number is printed on the side of the package under the bar code.

CPSCJan 30, 2025Nationwide• Pearhead, of Brooklyn, New York

Dark Chocolate Pretzels (Woodstock Farms) – Undeclared Milk (2025)

Undeclared Allergen

Undeclared Allergen - Milk

Class IHigh

FDAJan 27, 2025NY• United Natural Trading Inc. dba Woodstock Farms

Pre-Blend (Bridgewell Agribusiness) – Foreign Material (2025)

Foreign material appears to be white nylon or other plastic thread was found in product.

Class IIModerate

FDAJan 23, 2025IN, NY• Bridgewell Agribusiness LLC

RayStation Planning System (RaySearch) – density uncertainty (2025)

Inconsistency in the use of Density uncertainty in the RayStation functions Robust optimization, Robust evaluation and Compute perturbed dose for proton and light ion treatment plans when a HU-to-mass density CT calibration curve used in RayStation version 4.5 to 2024B including some service packs.

FDAJan 16, 2025Nationwide• RAYSEARCH LABORATORIES AB Eugeniavagen 18c Stockholm Sweden

Spartan Fire MetroStar (Marion) – cab tilt mechanism (2025)

Fire/Burn Risk

Marion Body Works Inc. (Marion Body Works) is recalling certain 2024 Spartan Fire Metro Star vehicles. A missing mechanical stop may allow the cab tilt cylinder to be overextended.

NHTSAJan 15, 2025Nationwide• MARION BODY WORKS

Nobel Biocare N1 TiUltra (Nobel) – Packaging Defect (2025)

Due to manufacturing issue (unintended by-product of the injection molding process) a sharp pin that may puncture the blister packaging and breaching the sterile barrier of the finished product.

FDAJan 10, 2025Nationwide• Nobel Biocare Vastra Hamngatan 1 Goteborg Sweden

Organic Almonds (Woodstock) – Mislabeled Product (2025)

Product mislabeled. The back label states Organic Cashews. The front product label states Wegmans Organic unsalted dry roasted almonds. The front label is correct label for this product.

Class IIModerate

FDAJan 6, 2025NY, PA, VA• United Natural Trading Inc. dba Woodstock Farms

VARIPULSE Ablation Catheter (Biosense) – Neurovascular Events (2025)

Due to an observed trend of neurovascular events

FDAJan 5, 2025AR, CA, CO +7 more• Biosense Webster, Inc.

CryoSolutions Cartridges (New Medical Technologies) – Valve Premature Opening (2024)

During the assembly of the cartridge to its connecting body part, the valve may open prematurely resulting in partial or complete emptying of the cartridge before its intended use.

FDADec 19, 2024Nationwide• New Medical Technologies Gmbh Wankdorffeldstrasse

Idylla Instrument (Biocartis) – False-Positive MSI-H Results (2024)

False-positive MSI-H results generated by the Idylla MSI Test.

FDADec 10, 2024AL, CA, NJ +2 more• Biocartis Nv B 3 Generaal De Wittelaan 11 Mechelen Belgium

BMW X3 (BMW) – Front Wheel Swivel Bearing Crack (2024)

BMW of North America, LLC (BMW) is recalling certain 2025 X3 30 vehicles. The front wheel left-side swivel bearing may crack, causing a loss of vehicle handling and control.

NHTSADec 5, 2024Nationwide• BMW

BMW X4 (BMW) – Roof Frame Air Bag Mounting Defect (2024)

BMW of North America, LLC (BMW) is recalling certain 2025 X4 xDrive 30i, X4 M40i and X4 M vehicles. The inner-left roof frame near the head air bag may have a crack that can damage the head air bag during deployment.

NHTSADec 5, 2024Nationwide• BMW

Ultrasoft Oxygen Cannula (3B Medical) – Expired Product (2024)

The devices were inadvertently shipped after their expiration date.

FDANov 27, 2024AR, MA• 3B Medical, Inc. 203 Avenue A Nw Ste 300 Winter Haven FL 33881-4540

Otological Ventilation Tube (Adept Medical) – Clearance Issue (2024)

Lack of 510(k) clearance.

FDANov 24, 2024Nationwide• Adept Medical Ltd 2-6 Mc Donald Street Morningside, Po Box 10075 Dominion Rd Auckland New Zealand

BMW 530i (BMW) – Airbag Control Unit (2024)

BMW of North America, LLC (BMW) is recalling certain 2025 530i and 540i xDrive vehicles. The air bag control unit may have been manufactured incorrectly, which can result in the air bags not deploying as intended.

NHTSANov 19, 2024Nationwide• BMW

Organic Whole Carrots (Grimmway Farms) – E. coli risk (2024)

E. coli

Potential contamination with E. coli O121:H19

Class IHigh

FDANov 16, 2024AL, AZ, AR +38 more• Grimmway Enterprises, Inc. dba Grimmway Farms