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Datex Ohmeda, Inc. dba GE Healthcare

Datex Ohmeda, Inc. dba GE Healthcare Recalls

All product recalls associated with Datex Ohmeda, Inc. dba GE Healthcare.

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Recall Summary

Total Recalls

1000

Past Year

442

Class I (Serious)

138

Most Recent

Dec 2025

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 7041–7060 of 7663 recalls

Datex Ohmeda, Inc. dba GE Healthcare: Corometrics MODEL 250 Series Maternal/ Fetal Monitor, Mod...

Communication connector within monitor is defective and may cause potential loss of telemetry.

FDAMay 5, 2008Nationwide• Datex Ohmeda, Inc. dba GE Healthcare

Bausch & Lomb Inc: Zyoptix XP Microkeratome tray, Ref. #ZXP1000, which conta...

The plastic tip on the drive shaft may come off the shaft and cause the blade to stop oscillating.

FDAApr 23, 2008Nationwide• Bausch & Lomb Inc

Bausch & Lomb Inc: Zyoptix XP Microkeratome maxon motor, Ref #ZXP09183. The...

The plastic tip on the drive shaft may come off the shaft and cause the blade to stop oscillating.

FDAApr 23, 2008Nationwide

1...351 352353354 355...384

Page 353 of 384Next

• Bausch & Lomb Inc

Beco Butterfly Baby Carriers – Safety Concern (2008)

The recalled infant carriers were sold under brand name "Beco Baby Carrier Butterfly." The carriers have a black label with a green "b" logo on the left side and a butterfly on the right side. The label is sewn on the outside of the carrier. The following carrier styles are included in the recall: Mia, Pony Express, Carnival, Addison, Ethan, Sophia, Cameron, Ava and Joshua.

CPSCApr 22, 2008Nationwide• Beco Baby Carrier Inc., of Newport Beach, Calif.

Advanced Bionics Corporation 12740 San Fernando Rd Bldgs. 1 & 3 Sylmar CA 91342: OMG (Observational Mechanical Gateway) Connector - A Mode...

The recall was initiated because there is a possibility that the OMG Connector-A is incorrectly packaged with an OMG Connector-M Instruction manual.

FDAApr 22, 2008Nationwide• Advanced Bionics Corporation 12740 San Fernando Rd Bldgs. 1 & 3 Sylmar CA 91342

Lithium-Polymer Battery Chargers (Art-Tech) – Fire Risk (2008)

Fire/Burn Risk

The recall involves a lithium-polymer battery charger and batteries sold with the AT600 Falcon Helicopter kit. The recall also includes any spare battery (Model AT600B) or spare charger (Model ATS6046) purchased for this kit.

CPSCApr 14, 2008Nationwide• Art-Tech R/C Hobby Co., Ltd. of Shenzhen, China

Medical Components, Inc dba MedComp: USCT5D, Pro-PICC CT 5F x 55 cm Dual Lumen. infusion cathe...

kit contains incorrect component

FDAApr 11, 2008IN, PA, TX• Medical Components, Inc dba MedComp

Medical Components, Inc dba MedComp: CMS-MST572 5F insertion kit with 5 cm tearaway. The produ...

kit contains incorrect component

FDAApr 11, 2008IN, PA, TX• Medical Components, Inc dba MedComp

Serenity Spa Hot Tubs (Gecko Alliance) – electrical fire hazard (2008)

Fire/Burn Risk

This recall involves the Hydropool Serenity Series Spa hot tubs with serial numbers 01350XXXX through 03210XXXX. The serial numbers are printed on the right side of the spa control. The Gecko spa control (SSPA-1) has model number 0202-205097 printed on it.

CPSCApr 1, 2008Nationwide• Gecko Alliance of Quebec, Canada

Celsus Laboratories Inc: Celsus Laboratories Heparin Lithium Lyophilized; Lithium ...

Contamination: The firm learned that up to 2.2% oversulfated chondroitin was found in a batch of crude heparin they received from their supplier.

FDAMar 31, 2008IN, NE, NJ +2 more• Celsus Laboratories Inc

Bausch & Lomb Inc: Bausch & Lomb Millennium Phacoemulsification Needles, Nee...

The directions for use are printed with the incorrect symbols to indicate the product is packaged as sterile and nonreusable

FDAMar 26, 2008Nationwide• Bausch & Lomb Inc

Bausch & Lomb Inc: Bausch & Lomb Millenium Phacoemulsification Needles, Need...

The directions for use are printed with the incorrect symbols to indicate the product is packaged as sterile and nonreusable

FDAMar 26, 2008Nationwide• Bausch & Lomb Inc

Abbott Vascular-Cardiac Therapies dba Guidant Corporation: 6F Viking Guiding Catheter, Percutaneous catheter, Shape ...

Mislabeling: The part number on the product label packaging may not match the product.

FDAMar 17, 2008Nationwide• Abbott Vascular-Cardiac Therapies dba Guidant Corporation

Edwards Lifesciences AG Parque Industrial Itabo Km. 18.5 Carr. Sanchez Haina, San Cristobal Dominican Republic: Edwards Lifesciences "VAMP Jr" (Venous Arterial blood Man...

Edwards Lifescience initiated a recall of on Edwards "VAMP Jr" Pressure Monitoring Products manufactured between 8/01/06 and 2/29/08 due to the potential for the cap on the reservoir of the "VAMP Jr" to become disconnected.

FDAMar 14, 2008PR• Edwards Lifesciences AG Parque Industrial Itabo Km. 18.5 Carr. Sanchez Haina, San Cristobal Dominican Republic

Cardinal Health 303 Inc DBA Alaris Products: U19 Socketed Integrated Circuit ("U19 IC") on the logic b...

A channel error on an affected Alaris System module will stop an active infusion (or monitoring) with an audible and visual alarm. Channel errors due to failures of the U19 Socketed Integrated Circuits (U19 IC) on the logic board of the Alaris Pump module ("Pump module"). The user will be required to replace the affected module.

FDAMar 5, 2008AZ, AR, CA +37 more• Cardinal Health 303 Inc DBA Alaris Products

Cardinal Health 303 Inc DBA Alaris Products: U9 Socket Integrated Circuit ("U9 IC") on the display boa...

A channel error on an affected Alaris System module will stop an active infusion (or monitoring) with an audible and visual alarm. Channel errors due to failure of the U9 Socketed Integrated Circuits (U9 IC) on the display board of the Alaris Syringe Module ("Syringe module") and Alaris PCA module ("PCA module") for modules manufactured on or before October 4, 2005. The user will be required to re

FDAMar 5, 2008AZ, AR, CA +37 more• Cardinal Health 303 Inc DBA Alaris Products

Cardinal Health 303 Inc DBA Alaris Products: Grey Inter-Unit Interface Connectors ("IUI") on the follo...

A channel error on an affected Alaris System module will stop an active infusion (or monitoring) with an audible and visual alarm. Channel errors with the Alaris System due to the Inter-Unit Interface (IUI) connectors on all Alaris System modules (manufactured on or before March 26, 2004). Grey Inter-Unit Interface Connectors ("IUI") on the following Alaris System modules built on or before March

FDAMar 5, 2008AZ, AR, CA +37 more• Cardinal Health 303 Inc DBA Alaris Products

Med Tec Inc dba CIVCO Medical Solutions: Fiducial Markers (0.9 x 3 mm) Soft tissue gold markers, M...

Mislabeled: Fiducial markers were incorrectly labeled. They are marked (0.9x3mm cylindrical) Soft tissue gold markers, but contain (2mm spheres) Bone gold markers.

FDAFeb 28, 2008Nationwide• Med Tec Inc dba CIVCO Medical Solutions

Med Tec Inc dba CIVCO Medical Solutions: Fiducial Markers (2mm spheres) Bone gold markers, Medical...

Mislabeled: Fiducial markers were incorrectly labeled. They are marked (2mm spheres) Bone gold markers, but contain (0.9x3mm cylindrical) Soft tissue gold markers.

FDAFeb 28, 2008Nationwide• Med Tec Inc dba CIVCO Medical Solutions

Boston Scientific Corporation One Boston: Boston Scientific Mach 1 Guide Catheter 6F, IM Internal M...

Mislabeled: Seven lots/ batches of Boston Scientific Mach 1 Guide Catheter may be mislabeled with the incorrect device length.

FDAFeb 7, 2008AL, AZ, AR +21 more• Boston Scientific Corporation One Boston