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
/
CTS, Inc. dba Guidant Cardiac Surgery

CTS, Inc. dba Guidant Cardiac Surgery Recalls

All product recalls associated with CTS, Inc. dba Guidant Cardiac Surgery.

Get alerts for this brand

Recall Summary

Total Recalls

1000

Past Year

421

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 3981–4000 of 4599 recalls

CTS, Inc. dba Guidant Cardiac Surgery: VASOVIEW 4 Endoscopic Vessel Harvesting System, with VASO...

Packaging unsealed: Sterility of product may be compromised due to packaging issue. For further information, please contact the firm at 408-635-6874.

FDASep 9, 2008Nationwide• CTS, Inc. dba Guidant Cardiac Surgery

GE Medical Systems, LLC: GE Healthcare Infinia Hawkeye(R), Model numbers: H2508PY ...

There is a possibility for misregistration when brain scans are performed with Infinia with the Hawkeye option. This misregistration could present the potential for misdiagnosis when the patient headrest sags under the weight of a head.

FDASep 8, 2008AL, AK, AZ +44 more• GE Medical Systems, LLC

Gebauer Company: Gebauer's Fluro-Ethyl Nonflammable Topical Anesthetic Ski...

Some units of Fluro-Ethyl containing the defective valve which could malfunction and spray refrigerant out from the side of the valve in addition to or instead of spraying in the normal inverted position from the product's actuator. The product can also leak coolant from the side of the valve onto the fingers of the user.

1...198 199200201 202...230

Page 200 of 230Next

FDASep 3, 2008Nationwide• Gebauer Company

GE Medical Systems, LLC: GE Healthcare, Drapes and Sterile Covers PART NUMBER ...

GE Healthcare has found that the sterile products manufactured by Contour Fabricators, Inc. (CFI) for GE healthcare (GEHC) may have sterile seals that could be compromised during the shelf life of the products. This issue could result in the product not maintaining its sterile state.

FDAAug 29, 2008Nationwide• GE Medical Systems, LLC

Stille AB Gardsvagen: Sonesta 6210 Fluoroscopy Procedure Table; a motorized pro...

The table contains a battery backup, not mentioned in the User Manual, which automatically will provide power to the electrical actuators/motions in case of a power loss from the main power supply. However, if a short circuit occurs, it can result in an uncontrolled movement of the table which cannot be stopped by disconnecting the device from the main power supply, as the battery automatically w

FDAAug 27, 2008Nationwide• Stille AB Gardsvagen

Draeger Medical, Inc.: Draeger Medical Apollo Anesthesia Machine, catalog number...

Sporadic errors in various device functions, including low readings of the single gas flows for oxygen, nitrous oxide, or air delivery, or mechanical ventilation failure. Alarms and error messages function as designed.

FDAAug 22, 2008Nationwide• Draeger Medical, Inc.

GE Medical Systems, LLC: Sterile, Drape, Headset, Upper, Part Number 888945-01.

GE Healthcare has found that the sterile products manufactured by Contour Fabricators, Inc. (CFI) for GE healthcare (GEHC) may have seals that could be compromised during the shelf life of the products. This issue could result in the product not maintaining its sterile state. Eleven complaints and 3 MDR's have been filed. No illness or injuries reported.

FDAAug 15, 2008Nationwide• GE Medical Systems, LLC

GE Medical Systems, LLC: Disposable Pack, Headset Part Number 888946-01(kit includ...

FDAAug 15, 2008Nationwide• GE Medical Systems, LLC

GE Medical Systems, LLC: Sterile, Drape, Headset, Lower, Part Number 888944-01.

FDAAug 15, 2008Nationwide• GE Medical Systems, LLC

GE Medical Systems, LLC: GE Medical Systems, OEC, Vascular Drape, 00-902776-01, St...

FDAAug 15, 2008Nationwide• GE Medical Systems, LLC

Smith And Nephew, Inc. Wound Management Division: GlobTek, Inc. Power Supply for Medical Use Part No: TR9CE...

External battery chargers used with the Version 29 VISTA Negative Pressure Wound Therapy pumps are failing to properly charge the pump's battery.

FDAAug 7, 2008Nationwide• Smith And Nephew, Inc. Wound Management Division

GE Healthcare: Innova 4100 / 4100 IQ , GE Healthcare, Waukesha, WI 53188...

The charger and / or battery of the PDB may fail earlier than expected with no advance warning and thus cause the system to shut down.

FDAJul 25, 2008Nationwide• GE Healthcare

GE Healthcare: Innova 2100IQ (The Digital Fluoroscopic Imaging System co...

The charger and / or battery of the PDB may fail earlier than expected with no advance warning and thus cause the system to shut down.

FDAJul 25, 2008Nationwide• GE Healthcare

GE Healthcare: Innova 2000; The principle system components include a C-...

The charger and / or battery of the PDB may fail earlier than expected with no advance warning and thus cause the system to shut down.

FDAJul 25, 2008Nationwide• GE Healthcare

GE Healthcare: Innova 3100 / 3100 IQ, Cardiovascular Imaging System, GE ...

The charger and / or battery of the PDB may fail earlier than expected with no advance warning and thus cause the system to shut down.

FDAJul 25, 2008Nationwide• GE Healthcare

Reebok Studio Exercise Cycles – Laceration Risk (2008)

Laceration Risk

The Reebok Studio Cycle is an upright exercise bike used primarily in fitness centers and other institutional settings. The recalled bicycle is black with silver cranks. The unit has an internal belt drive. The base of the bicycle is a single piece that is welded to the frame. The legs are two straight horizontal bars with rounded edges. There is a logo located on the side of the exercise cycle that shows a person riding a bicycle.

CPSCJul 24, 2008Nationwide• Fitness Associates Incorporated (F.A.I.), under license from Reebok International Ltd., of Canton, Mass. Note: F.A.I. is no longer in business.

Walther Air Pistol Cylinders – Burst Risk (2008)

The recalled Walther air cylinders for air pistols are aluminum and involve model 2/WALTHER 85 cm3, with the imprinted test date between 6 00 and 6 01 2000/2001 located on the end of the cylinder.

CPSCJul 23, 2008Nationwide• Carl Walther GmbH, Sportwaffen, of Germany

BD Diagnostics (GeneOhm Sciences, Inc): BD GeneOhm MRSA 200 ct, Catalog #441242. IDI-MRSA assay...

BD Diagnostics GeneOhm (BDDG) initiated the recall after they identified that the product has the potential to identify a patient as falsely positive for colonization with methicillin resistant Staphylococcus aureus. The potential health hazard related to a false positive result from this assay would be that a patient may be misclassified as having MRSA colonization when in fact they do not have

FDAJul 21, 2008Nationwide• BD Diagnostics (GeneOhm Sciences, Inc)

BD Diagnostics (GeneOhm Sciences, Inc): BD GeneOhm MRSA 48 ct, Catalog #441244. IDI-MRSA assay i...

FDAJul 21, 2008Nationwide• BD Diagnostics (GeneOhm Sciences, Inc)

Apogee Medical, Inc: Apogee Intermittent Catheter, 10 Fr 15", Catalog/Ref No. ...

Laceration Risk

Due to a package seal defect the catheter tip may have been inadvertently cut which could cause trauma to the urethra upon use. Also the sterility of the product could be compromised.

FDAJul 17, 2008Nationwide• Apogee Medical, Inc