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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.

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Recall Summary

Total Recalls

1000

Past Year

1000

Class I (Serious)

143

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 34201–34220 of 37665 recalls

Abbott Vascular-Cardiac Therapies dba Guidant Corporation: ACS DUOSTAT Rotating Hemostatic Valve, 0.096 inch, for us...

Specific lots of the .096' and .115' Rotating Hemostatic Valves (RHV) and the Duostat .096' Rotating Hemostatic Valve (RHV) potentially have an incomplete seal in the packaging pouch

FDADec 5, 2006Nationwide• Abbott Vascular-Cardiac Therapies dba Guidant Corporation

Abbott Vascular-Cardiac Therapies dba Guidant Corporation: ACS Rotating Hemostatic Valve, 0.096 inch, for use with a...

Specific lots of the .096' and .115' Rotating Hemostatic Valves (RHV) and the Duostat .096' Rotating Hemostatic Valve (RHV) potentially have an incomplete seal in the packaging pouch

FDADec 5, 2006Nationwide• Abbott Vascular-Cardiac Therapies dba Guidant Corporation

Synthes: LCP Volar Distal Radius Plate Extra Articular 4H HD-RT-Lo...

Hole is malformed, leading to reduced construct strength.

1...1709 171017111712 1713...1884

Page 1711 of 1884Next

FDADec 5, 2006CA, IN, KS +5 more• Synthes

Door Handle Locks (Stanley) – Entrapment Risk (2006)

The recalled units include the 5K Light/Medium Duty Lever Series door handle locks. These sets have a brass or stainless steel finish with the word "BEST" embossed below the key whole on the elongated handle.

CPSCDec 5, 2006Nationwide• Stanley Security Solutions Inc., of Indianapolis, Ind.

Diagnostic Chemicals, Ltd.: Salicylate-SL, in vitro diagnostic, Cat. No.511-20, Lot N...

Upon subsequent testing on different instruments (as required by other customers), DCL detected a non-linear response on certain analyzers. A decision was made to recall the product due to the fact that DCL customers sell the product to different end users, DCL cannot be certain which instruments the end users employ in their laboratories

FDADec 5, 2006PA• Diagnostic Chemicals, Ltd.

Stryker Howmedica Osteonics Corp.: Triathlon X3 CR Tibial Bearing Insert for knee prosthesis...

A product mix-up in which the labeling indicates a Triathlon X# CR Tibial Bearing Insert Size #2 - 11MM, however, the device inside the package is actually a Triathlon X3 CR Tibial Bearing insert Size # 7 - 11MM and vice versa.

FDADec 4, 2006Nationwide• Stryker Howmedica Osteonics Corp.

Stryker Howmedica Osteonics Corp.: Triathlon X3 CR Tibial Bearing Insert Size #7 - 11MM Ref ...

A product mix -up in which the labeling indicates a Triathlon X# CR Tibial Bearing Insert Size #2 - 11MM, however, the device inside the package is actually a Triathlon X3 CR Tibial Bearing insert Size # 7 - 11MM and vice versa.

FDADec 4, 2006Nationwide• Stryker Howmedica Osteonics Corp.

Boston Scientific Target: Boston Scientific brand iLab Ultrasound Imaging System, ...

The product fails to comply with applicable electronic product performance standard, in that the electromagnetic energy is in excess of the labeled conformance standards for radiated emissions.

FDADec 1, 2006Nationwide• Boston Scientific Target

Guidant Cardiac Surgery: Guidant Acrobat Vacuum Stabilizer, Model Number OM-9000.

Vacuum Tubing Failure- vacuum tubing fails before the labeled two year shelf life. This may result in partial or complete vacuum loss during surgery.

FDADec 1, 2006Nationwide• Guidant Cardiac Surgery

Stardental Division: Solara Replacement Turbine, Autochuck End Cap, for dental...

End cap component can disassemble.

FDADec 1, 2006Nationwide• Stardental Division

Air Conditioners (Trane) – Smoking Units (2006)

The recall includes 208-, 230- and 265-volt models of the Trane PTEE and PTHE Series Packaged Terminal Air Conditioners (PTACs). They were manufactured from about March 2006 through July 2006. The date code is F06C through F06G, and is written on the unit's Manufacturer's Data Plate located behind the molded plastic cover above the power connection. The units have the following model numbers, also written on the Manufacturer's Data Plate: PTEE0701UAA PTEE1501UAA PTHE0902UAA PTEE0702UAA PTEE1502UAA PTHE1201UAA PTEE0901UAA PTHE0701UAA PTHE1202UAA PTEE0902UAA PTHE0702UAA PTHE1501UAA PTEE1201UAA PTHE0901UAA PTHE1502UAA PTEE1202UAA

CPSCNov 30, 2006Nationwide• Qingdao Haier Air Conditioner, of Qingdao, China

Stryker Howmedica Osteonics Corp.: Howmedica Hip Fracture Stem System, Product Number: 6942-...

Lack of assurance of Sterility (package integrity): Anomalies in seal width and strength that may affect the integrity of the sterile barrier.

FDANov 28, 2006Nationwide• Stryker Howmedica Osteonics Corp.

Baxter Healthcare Corp. Rt.: Baxter Flo-Gard 6200 Volumetric Infusion Pump, catalog #2...

There is the potential for non-detection of, and no alarm for, upstream occlusion for Flo-Gard Volumetric Infusion Pumps, if an occlusion occurs above a flexible chamber such as a drip chamber, Buretrol or blood filter.

FDANov 27, 2006PR• Baxter Healthcare Corp. Rt.

Plus Orthopedics USA: VKS Tibial Trial, Right/Left, Prep Guide; Model Number: ...

The VKS "Tibial Trial" was found to have an incorrect fixation pin hole diameter.

FDANov 27, 2006Nationwide• Plus Orthopedics USA

Edwards Lifesciences Technology SARL: Edwards Lifesciences-Swan-Ganz,Thermodilution Venous Infu...

Misbranding-One lot of Swan-Ganz Thermodilution VIP Catheters, Model 831HF75, lot 246HC197 was labeled with different model information (831F75) on the edge label . The edge label states the model is 831F75 which incorrectly indicates that product does NOT contain an antimicrobial heparin coating. (The tray lid label correctly states the model is 831HF75, containing the heparin coating)

FDANov 27, 2006Nationwide• Edwards Lifesciences Technology SARL

Baxter Healthcare Corp. Rt.: Baxter Flo-Gard 6201 Volumetric Infusion Pump, catalog #2...

FDANov 27, 2006PR• Baxter Healthcare Corp. Rt.

Baxter Healthcare Corp. Rt.: Baxter Flo-Gard 6300 Dual Channel Volumetric Infusion Pum...

FDANov 27, 2006PR• Baxter Healthcare Corp. Rt.

Baxter Healthcare Corp. Rt.: Baxter Flo-Gard 6301 Dual Channel Volumetric Infusion Pum...

FDANov 27, 2006PR• Baxter Healthcare Corp. Rt.

Fisher & Paykel Healthcare Inc: Fisher & Paykel Oracle Oral Mask, Part Numbers: 900HC451,...

Plastic tabs incorporated into the connector components of these CPAP masks may break off if they are not cleaned in accordance with the Instructions for Use. In the event of a tab breaking off, it may enter the CPAP system air path and there is an extremely remote possibility that the broken tab may then enter the patient's nasal cavity or mouth. Masks manufactured since April 2006 do not feat

FDANov 24, 2006Nationwide• Fisher & Paykel Healthcare Inc

Fisher & Paykel Healthcare Inc: Fisher & Paykel Spares CPAP Mask and Connectors, Part Num...

FDANov 24, 2006Nationwide• Fisher & Paykel Healthcare Inc