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General Electric Med. Sys. Ultrasound

General Electric Med. Sys. Ultrasound Recalls

All product recalls associated with General Electric Med. Sys. Ultrasound.

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Recall Summary

Total Recalls

1000

Past Year

426

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 4301–4320 of 4598 recalls

General Electric Med. Sys. Ultrasound: Voluson 730 Expert, Voluson 730 Pro, Voluson 730 ProV wit...

In the cardiac measurement section of the device the calculation of the 'PG Mean' (mean pressure gradient) leads to an erroneous result. It is recommended that customers with affected units do not use the measurement in question 'PG Mean' for any diagnostic or therapeutic decision, and 'PG Mean' values should not be included in any patient documentation.

FDAFeb 24, 2006Nationwide• General Electric Med. Sys. Ultrasound

Silk Kimono Tops (Single) – Product Issue (2006)

Fire/Burn Risk

The recall involves the Silk Kimono Top, sold as catalog/Web site item number 194-860. This is a two-piece garment with a kimono outer shell and an orange inner camisole. The outer shell's sewn in label states the following: "Single, 100% Silk, RN 80763, Made In USA, Dry Clean Only." A separate label shows the item number 194-860. The Silk Kimono Tops were sold in paisley print pattern with metallic threads.

CPSCFeb 23, 2006Nationwide• Single, of Los Angeles, Calif.

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Biogenex Laboratories: Test kit used in the assessment of breast cancer patients...

Products produce granular staining in immunostained tissue sections, which may lead to misdiagnosis due to false positive result.

FDAFeb 9, 2006Nationwide• Biogenex Laboratories

GE Medical Systems Information Tecnology 9900 Inovation Drive RP 2122 3rd Floor Wauwatosa WI 53226: Datex-Ohmeda S/5 Critical Care Monitor with L-CICU01, L...

GE Healthcare (Datex-Ohmeda) S/5 Critical Care Monitor and S/5 Compact Critical Care Monitor with L-CICU01, L-CICU02A, L-ICU05 & L-ICUO5A software had an issue where the Heart Rate (HR) was displaying as ---(3 dashes) when the monitor was used continuously for 49 days without a cold start. A missed alarm or missed HR value could cause a delay in recognition of a cardiac event that may result i

FDAFeb 6, 2006IA, PR• GE Medical Systems Information Tecnology 9900 Inovation Drive RP 2122 3rd Floor Wauwatosa WI 53226

GE Medical Systems Information Tecnology 9900 Inovation Drive RP 2122 3rd Floor Wauwatosa WI 53226: Datex-Ohmeda S/5 Compact Critical Care Monitor with L-CIC...

FDAFeb 6, 2006IA, PR• GE Medical Systems Information Tecnology 9900 Inovation Drive RP 2122 3rd Floor Wauwatosa WI 53226

GE OEC Medical Systems, Inc: GE Healthcare Navigation Pin Transmitter (GE P/N 1004070)...

Small retaining pin may detach and fall into the surgical field during stereotactic surgery.

FDAFeb 6, 2006AL, AZ, CA +23 more• GE OEC Medical Systems, Inc

Baby Walkers (SunTome) – Stairway Fall Risk (2006)

The recalled walkers have eight wheels and are sold in various colors including dark blue, pink and white, or pink and red. The activity trays on the baby walkers have a steering wheel, various rattles and a mirror or animal themes. The trays play music when the baby pushes a button. "Baby" is printed on a sticker on the tray or the walker's base.

CPSCFeb 1, 2006Nationwide• SunTome Trading Corp., of Los Angeles, Calif.

Medtronic Emergency Response Systems, Inc.: LIFEPAK 500 automated external defibrillator (AED)

Component leads may have intermittent connection to the printed circuit board assembly pads - which could render the device inoperative.

FDAFeb 1, 2006Nationwide• Medtronic Emergency Response Systems, Inc.

Medtronic Emergency Response Systems, Inc.: LIFEPAK EXPRESS defibrillator

One of the printed circuit board assemblies may be contaminated with solder flux which can cause a short that may render the device inoperative.

FDAJan 31, 2006Nationwide• Medtronic Emergency Response Systems, Inc.

Medtronic Emergency Response Systems, Inc.: LIFEPAK CR Plus defibrillator

One of the printed circuit board assemblies may be contaminated with solder flux which can cause a short that may render the device inoperative.

FDAJan 31, 2006Nationwide• Medtronic Emergency Response Systems, Inc.

General Electric Med Systems LLC: Discovery ST PET/CT imaging system with gantry model numb...

The LightSpeed CT Technical Reference Manual was omitted from the document kit shipped with the PET/CT system.

FDAJan 26, 2006Nationwide• General Electric Med Systems LLC

Guardian Generator Fuel Hoses – Safety Concern (2006)

Fire/Burn Risk

The recalled 12-inch braided flex fuel hoses are used with Guardian® Home Standby Air-Cooled Generators with serial numbers 3789827 and below. The generators are about 4 feet by 2 feet by 2½ feet, tan in color, and have identification decal tags displaying the serial number. The decal tag is affixed to the black divider plate that separates the engine from the control panel and can be found by lifting the top/lid of the metal enclosure. The fuel hose came supplied with the generator kits and connects the fuel supply to the generator. The hose is 12 inches long and covered with braided steel.

CPSCJan 11, 2006Nationwide• Generac Power Systems Inc., of Waukesha, Wis. (generator)

Draeger Medical, Inc.: Babylog 8000 plus with software version 5.n. Neonatal Res...

Failure to generate an alarm when an unintended disconnection occurrs

FDADec 28, 2005Nationwide• Draeger Medical, Inc.

Aspen 3-in-1 Cribs (Graco) – Suffocation Risk (2005)

The recalled cribs are made of wood and have a wooden mattress support. Only cribs with wooden mattress supports and with model number 8740KCW SC and serial number 2803 SC to 1605 are included in this recall. The model and serial number are printed on the envelope attached to the mattress support.

CPSCDec 21, 2005Nationwide• Simplicity Inc., of Reading, Pa. (The firm appears to no longer conduct day to day operations)

GE Monogram Gas Ranges – Fire Hazard (2005)

Fire/Burn Risk

The recalled GE Monogram built-in ranges include models ZDP48N6RH1SS, ZDP48L6RH1SS, ZDP48N4GH1SS, ZDP48L4GH1SS, ZDP48N6DH1SS, ZDP48L6DH1SS, ZDP36N4DH1SS, and ZDP36L4DH1SS. The recalled ranges have serial numbers starting with DG, FG, GG, HG, LG, MG, RG, SG, TG, VG, ZG, AH, DH, FH, GH, HH, LH, MH, RH, SH. To find the model and serial number, look underneath the top ledge (also called the "bull nose"), above the range controls. They were manufactured from February 1, 2004 to October 1, 2005.

CPSCDec 15, 2005Nationwide• GE Consumer & Industrial, of Louisville, Ky.

Children's Activity Books (Advantage) – Potential Hazard (2005)

Choking Hazard

The recalled children's activity books are multi-colored, with holes in the pages to touch a variety of fabrics and to push a squeaker toy, flaps to lift, and a clear plastic container with beads. The "Amazing Baby Look and Play" activity book has a yellow star on the cover. The "Amazing Baby Touch and Play" book has a brown bear on the cover. The activity books measure about 11 inches by 11 inches, and are for children ages 12 months to 24 months. The recalled "Rattle, Rattle" board book has a magenta car on the cover. The board book measures about 5½ inches by 5½ inches, and is intended for children ages 6 months to 18 months.

CPSCDec 15, 2005Nationwide• Advantage Publishers Group, of San Diego, Calif.

General Electric Med Systems LLC: Diamond Mammographic X-Ray System, type MGX-2000, model ...

GE Healthcare has become aware of the absence of thread-locking compound associated with the C-arm fasteners of your Diamond mammographic x-ray system that may impact patient safety.

FDANov 16, 2005Nationwide• General Electric Med Systems LLC

GE Healthcare: Datex-Ohmeda S/5 Anesthesia Delivery Unit (ADU)

Alarm sound-It is possible that the audible alarms from the speaker from the Datex-Ohmeda S/5 Anesthesia Delivery Unit (ADU) machine may dampen or disappear as a result of normal handling of the anesthesia machine. Visual alarms on the ADU are unaffected by this condition. The dampening or absence of audible alarms on the ADU may result in a delay in treatment.

FDANov 16, 2005AZ, CA, IA +3 more• GE Healthcare

Jumbo Pencils with Sharpeners (Target) – Potential Safety Issue (2005)

Laceration Risk

The jumbo pencil has a red eraser on the end and comes with a pencil sharpener. Pencils are either short, 8 ½ inches long and one inch wide, or long, 15 inches long and ½ inch wide. The pencils are blue, red or striped. The sharpeners are pink or blue and come in a clear plastic pouch. Model number 70505 is printed on the pouch.

CPSCOct 18, 2005Nationwide• Target Corp., of Minneapolis, Minn.

Regeneration Technologies, Inc.: Product is 1.0 cc Regenaform RT. Product is labeled in...

The tissue was collected from donors for whom there is no verifiable identity or consent. The medical records and social histories of the donors cannot be ascertained. The devices which incorporate these donor bone tissues undergo processing, including sterilization, which has been validated to inactivate and/or remove all viral diseases for which human tissue donors are tested.

FDAOct 14, 2005Nationwide• Regeneration Technologies, Inc.