Recall of GE
Voluson IC9-RS Intracavity Probes

According to the U.S. Food and Drug Administration, this recall involved a device in the United States that was produced by GE Healthcare.

WHAT IS THIS?

A Recall is a firm’s removal or correction of a marketed product that the FDA considers to be in violation of the laws it administers and against which the agency would initiate legal action, e.g., seizure. Recall does not include a market withdrawal or a stock recovery.

EVENT
Type of EventRecall
Recall NumberZ-0865-2024
Risk ClassClass 2
Recall Qty12,004
Classification Date2024-01-30
Recall LinkRecall Link
Notes/AlertsN/A
Recall ReasonIssue can result in a double image artifact creating a ghost image with realistic features.
DEVICE
ManufacturerGE Healthcare
Model NameVoluson IC9-RS intracavitary probe
Model NumberJ48691PJ
Part/Item/Catalog/
REF/Product Number
-
Device DescriptionThe GE IC9-RS is an endocavity probe. This probe is used in gynaecological and obstetric examinations as well as in urological examinations.
Serial Number(s)1222552WX0, 1263125WX5, 1066771WX5, ...
Lot #/Exp Date(s)N/A
GE Voluson IC9-RS intracavity probe
GE Voluson IC9-RS intracavity probe
CUSTOMER/PATIENT ACTIONS

1. Ensure all potential users in your facility are made aware of this correction notification and the recommended actions.

2. You can continue to use your ultrasound system with all other probes.

3. Upon receipt of the letter, verify if your IC9-RS probe is functioning correctly prior to use by performing the Double Image artifact test provided in the letter. (Testing must be repeated monthly)

4. If a double image artifact is seen, do not use the probe and contact a GE HealthCare representative to get a replacement probe.

5. Complete and return the attached acknowledgement form to Recall.79072@ge.com. Please retain this document for your records.

CONTACT INFORMATION

Report any adverse health consequences experienced with the use of this product to BD. Events may also be reported to the FDA’s MedWatch Adverse Event Reporting program via:

Web: MedWatch website at www.fda.gov/medwatch

Phone: 1-800-FDA 1088 (1-800-332-1088)

Mail: MedWatch, HF-2, FDA, 5600 Fishers Lane, Rockville, MD 20852-9787

GE Voluson IC9-RS intracavity probe
GE Voluson IC9-RS intracavity probe
DISCLAIMER
Medical devices help to diagnose, prevent and treat many injuries and diseases. We are not suggesting or implying that any companies or other entities included in the Database engaged in unlawful conduct or otherwise acted improperly. The same device may have different names in different countries. This database is not intended to provide medical advice and patients should check with their doctors to determine if it contains relevant information and if such information has medical implications for them.

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