Stay Informed

Get email alerts when new recalls match your interests.

Recall data is updated hourly from official government sources. Very recent recalls may not yet appear. About our data sources

About

We make U.S. recall data searchable and accessible for consumers and businesses.

Site

FAQ
Browse by State
Statistics
Recall Classifications
About
Enterprise API

Legal

Privacy Policy
Terms of Service
Report Incorrect Info

Official Sources

FDA Recalls ↗
USDA FSIS ↗
CPSC Recalls ↗
NHTSA Recalls ↗

RSS Feed

Home
/
Brands
/
Abbott Vascular-Cardiac Therapies dba Guidant Corporation

Abbott Vascular-Cardiac Therapies dba Guidant Corporation Recalls

All product recalls associated with Abbott Vascular-Cardiac Therapies dba Guidant Corporation.

Get alerts for this brand

Recall Summary

Total Recalls

1000

Past Year

566

Class I (Serious)

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 6381–6400 of 7756 recalls

Abbott Vascular-Cardiac Therapies dba Guidant Corporation: Xact 10 mm x 20 mm x 136 cm (Part Number 82099-01) The X...

Abbott Vascular is initiating a recall on the XACT Carotid Stent System because the product was distributed prior to approval of a PMA supplement for a manufacturing line move between sites. There are no product quality issues associated with this action.

FDAMar 19, 2009Nationwide• Abbott Vascular-Cardiac Therapies dba Guidant Corporation

Brainlab AG Ammerthalstrasse 8 Kirchheim B. Muenchen Germany: BrainLab m3 Micro-Multileaf-Collimator for Varian Type II...

The Integrated Multileaf-Collimator (MLC) of the linear accelerator could interfere with the intended conformal fields of the BrainLab m3 micro-Multileaf-Collimator (mMLC) during patient treatment.

FDAMar 19, 2009Nationwide• Brainlab AG Ammerthalstrasse 8 Kirchheim B. Muenchen Germany

Brainlab AG Ammerthalstrasse 8 Kirchheim B. Muenchen Germany: BrainLab Micro-Multileaf-Collimator, model 41600; BrainLa...

1...318 319320321 322...388

Page 320 of 388Next

The Integrated Multileaf-Collimator (MLC) of the linear accelerator could interfere with the intended conformal fields of the BrainLab m3 micro-Multileaf-Collimator (mMLC) during patient treatment.

FDAMar 19, 2009Nationwide• Brainlab AG Ammerthalstrasse 8 Kirchheim B. Muenchen Germany

Abbott Vascular-Cardiac Therapies dba Guidant Corporation: Xact 9 mm x 20 mm x 136 cm (Part Number 82089-01) The Xa...

FDAMar 19, 2009Nationwide• Abbott Vascular-Cardiac Therapies dba Guidant Corporation

Boston Scientific Corporation: Boston Scientific, Flexima and Percuflex Drainage Cathete...

Boston Scientific Corporation is initiating an urgent Field Correction related to its Flexima and Percuflex Drainage Catheter Family (Pigtail Style). During the attempted removal of the device, sutures were separated from the catheter and remained in the patient.

FDAMar 18, 2009DC, PR• Boston Scientific Corporation

Zero Turn Riding Mowers (Kubota) – Fire Risk (2009)

Fire/Burn Risk

The recalled riding mowers are propelled by gasoline V-twin engines and have 48-inch, 54-inch or 60-inch wide mower decks. The mowers come with adjustable roll bars and have 22 or 27 horsepower engines and are bright orange with KUBOTA decals on both sides behind the driver's seat. This recall includes the following model numbers: ZG222(serial numbers 10002 through 13673), ZG227 (serial numbers 10002 through 12957), ZG327 (serial numbers 10004 through 13318) which can be identified by the model designation and serial number on the data plate located on the right side frame, either before the mower deck or immediately after the mower deck.

CPSCMar 17, 2009Nationwide• Kubota Manufacturing of America Corp., of Gainesville, Ga.

Abbott Diabetes Care, Inc.: FreeStyle Blood Glucose Monitoring System Test Strips and...

Product dispositioned for destruction was potentially diverted to end users.

FDAMar 13, 2009Nationwide• Abbott Diabetes Care, Inc.

Boston Scientific Corporation: Boston Scientific Wiseguide Guide Catheter, Sterilized. ...

Boston Scientific has initiated a recall of the Wiseguide Guide Catheter. They have received reports of difficulties in connecting the product hubs with the Y-Adaptors and toughy borst connectors. If there is difficulty making such connection, there is a potential for prolongation or delay of the procedure in order to exchange the catheter or connector. There have been 41 complaints in the US as

FDAMar 11, 2009PR• Boston Scientific Corporation

Hill-Rom, Inc. 125 E Pearl St 1069 State Route 46 East Batesville IN 47006: Hill-Rom TotalCare Bed, Model P1900. The TotalCare (R) B...

An e-ring may not have been installed during production, which could result in an inability to latch the siderail.

FDAMar 9, 2009Nationwide• Hill-Rom, Inc. 125 E Pearl St 1069 State Route 46 East Batesville IN 47006

Beckman Coulter Inc.: Access Immunoassay Systems Total hCG. The Access Total h...

The recall was initiated because Beckman Coulter has confirmed that certain Access Total hCG reagent packs show decreased stability from the date of manufacture, which may lead to increased imprecision.

FDAMar 5, 2009PR• Beckman Coulter Inc.

Cardinal Health 303 dba Cardinal Health: Alaris Patient-Controlled Analgesia (PCA) Module (formerl...

The Alaris PCA module can potentially infuse above or below the intended infusion dose.

FDAMar 4, 2009Nationwide• Cardinal Health 303 dba Cardinal Health

Abbott Laboratories: ARCHITECT Reaction Vessel, 2000 units per carton; for in ...

Abbott has had an increase in complaints due to the receipt of error code 1006 (unable to process test, background read failure), error code 1007 (unable to process test, activated read failure) and incorrect results when using these lots of ARCHITECT Reaction Vessels.

FDAFeb 26, 2009Nationwide• Abbott Laboratories

Scuba Diving Hoses (Ambient Pressure) – drowning risk (2009)

The crimped hoses are used to carry the air supply in the re-breathing diving system. The hoses were sold on three re-breathing models: Inspiration, Evolution and Evolution Plus. Hoses with a smooth (uncrimped) collar and with the model numbers listed below are included in the recall: AP300/15 ADV Supply Hose RB20/03 Oxygen Injection Hose EV20/03 Oxygen Injection Hose RB20/10 Buzzer Hose EV11A/1 Vision Handset Hose RB11A/1 Classic Handset Hose RB11/B Handset Hose AP300/10 ADV Hose AP300/38 ADV Hose Hoses with eight flats on the hose collar have been crimped and are not included in the recall.

CPSCFeb 24, 2009Nationwide• Ambient Pressure Diving Ltd., of Helston, Cornwall, United Kingdom

MDS Canada Inc. DBA MDS Nordion 447 March Road Ottawa Canada Ontario: TheraSphere Administration Set (Part Number K125914-034)....

Instructions for the use of the pinch clamp that is an integral part of the TheraSphere Administration Set were not included with the distribution of the device.

FDAFeb 24, 2009AZ, CA, CO +12 more• MDS Canada Inc. DBA MDS Nordion 447 March Road Ottawa Canada Ontario

Sybron Dental Specialties: Sealapex Express (Part Number: 33639), root canal filling...

Sybron Dental Specialties is initiating a recall on the Sealapex Xpress due to the presence of crystals in the catalyst. This crystallization may affect proper canal filling by preventing Gutta Percha Points from reaching the bottom of the root canal which may lead to an inadequate seal.

FDAFeb 23, 2009Nationwide• Sybron Dental Specialties

Sybron Dental Specialties: Herculite Ultra (Part Number 34333), dental composite res...

Sybron Dental Specialties is initiating a field correction on the Herculite Ultra, a dental composite restorative material, due to a mistake in the directions for use located in the Herculite technique card.

FDAFeb 23, 2009Nationwide• Sybron Dental Specialties

Abbott Laboratories: Abbott AxSYM Cancer Assay Disk Version 5.0, for in vitro ...

The AxSYM Cancer Assay Disk (LN 3D50-05 version 5.0) contains an AxSYM AFP assay file where the Low Concentration flag for the AFP 1:101 automated dilution protocol the instrument to report results between 0 ng/mL and 0.4 ng/mL (40.4 ng/mL accounting for the 1:101 dilution). The sensitivity of the assay is 0.4 ng/mL.

FDAFeb 20, 2009Nationwide• Abbott Laboratories

Biomet Microfixation, Inc.: Byrd Screw, 2.0X6MM SD, Model Number: 01-0264 Product lab...

Byrd Screw, Self Drilling, may break during usage. BIOMET has determined that the parts were not correctly processed by the vendor , i.e. that the parts were not hardened in the final processing and that lead to weaker than acceptable material.

FDAFeb 19, 2009AZ, CA, GA +7 more• Biomet Microfixation, Inc.

Beckman Coulter Inc.: SYNCHRON Gentamicin (GEN) Reagent GEN reagent, when used ...

The reagent produces false low test results. Beckman Coulter has confirmed low recovery of values at the low end of the therapeutic range (<1.5 ug/mL, <3.13 umol/L) with SYNCHRON Systems Gentamicin Reagent (GEN) lot M804552. A false low result can cause a patient to receive more medication than necessary.

FDAFeb 19, 2009AL, AZ, AR +42 more• Beckman Coulter Inc.

Abbott Laboratories: AxSYM System Tubing Decontamination Solution; 500 mL bott...

Bottle labels from lot 211974, AxSYM System Tubing Decontamination Solution (List Number 7B05-09), were found to be missing the following information: lot number, date of manufacture, and expiration date.

FDAFeb 18, 2009Nationwide• Abbott Laboratories