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Lithonia Lighting, of Conyers, Ga.

Lithonia Lighting, of Conyers, Ga. Recalls

All product recalls associated with Lithonia Lighting, of Conyers, Ga..

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Recall Summary

Total Recalls

1000

Past Year

593

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 9401–9420 of 10391 recalls

Lithonia Downlight Fixtures – Fire Risk (2008)

Fire/Burn Risk

The recalled fixture is a ceiling-mounted downlight. Model number LV3R is included in this recall and is printed on a UL label inside the light's housing.

CPSCJul 22, 2008Nationwide• Lithonia Lighting, of Conyers, Ga.

Spacelabs Healthcare, Incorporated: Ultraview SL Command Module, Model 90496 The product is i...

Potential for module to fail to obtain a NIBP reading on hypertension patients.

FDAJul 22, 2008Nationwide• Spacelabs Healthcare, Incorporated

Spacelabs Healthcare, Incorporated: Ultraview Digital Telemetry Transmitter, Model 90478 The ...

Telemetry Modules are failing to alarm for low heart rate and asystole.

1...469 470471472 473...520

Page 471 of 520Next

FDA

Jul 18, 2008

Nationwide

• Spacelabs Healthcare, Incorporated

Spacelabs Healthcare, Incorporated: Ultraview Digital Telemetry Transmitter, Model 91341-09 T...

During battery insertion there is potential for patient waveforms to move to an open receiver module or to an occupied receiver causing the intermittent inappropriate monitoring of both patients for several minutes.

FDAJul 17, 2008Nationwide• Spacelabs Healthcare, Incorporated

GE Healthcare Kuortaaneenkatu 2 Helsinki Finland: GE Healthcare, Mobile Care Server used in conjunction wit...

Issue 1 -Possible failure of CIC Pro audible alarms: Requests for telemetry defaults from Mobile Care Server could cause excessive CIC Pro memory consumption. This excessive memory consumption may lead to potential loss of audio at the CIC or a system reset or reboot. Issue 2 - Mobile Care software/Mobile Viewers don not recognize ApexPro FH Telemetry transmitter: Mobile Care server does not ac

FDAJul 16, 2008CA, IN, IA +2 more• GE Healthcare Kuortaaneenkatu 2 Helsinki Finland

Bench Scale Adapters – Fire Risk (2008)

Fire/Burn Risk

The recalled bench adapters are silver colored. "MINI CHARGER" is printed on the back of the adapter. When plugged in a red light shines through a blue plastic piece on the outer side of the adapter. "AC Adapter" is printed on a white label on the inner side. The adapters are used with bench scale model AMW-13, AMW-1000, AMW-2000, and AMW-500i.

CPSCJul 15, 2008Nationwide• American Weigh Scales, of Charleston, S.C.

Philips Medical Systems North America Co. Phillips: The Philips EasyDiagnost Eleva with DRF. Philips Medical...

Potential for bright artifacts to appear on the patient image from a previous exposure.

FDAJul 9, 2008AZ, CA, FL +2 more• Philips Medical Systems North America Co. Phillips

Philips Healthcare Informatics, Inc.: Philips Healthcare Informatics iSite PACS (Picture Archi...

Scout line and localizer crosshair on MPR images will display in the incorrect position under certain circumstances.

FDAJul 3, 2008Nationwide• Philips Healthcare Informatics, Inc.

Spacelabs Healthcare, Incorporated: Spacelabs Medical Temperature Probe Adaptor PN-700-0031-0...

Intermittent contact of temperature probe adaptors can cause a loss of temperature monitoring which can cause a delay in care when an alarm is missed.

FDAJul 2, 2008Nationwide• Spacelabs Healthcare, Incorporated

GE Healthcare: GE Stereotaxy Positioner, model 2405544-2, for use with ...

GE Healthcare has recently become aware of x-ray emission beyond the edge of the detector primary barrier. This issue occurs when an exam is performed in a specific angulated view associated with use of the Stereotactic Positioner of your Senographe DS Acquisition system and could impact patient safety. If the Stereotactic Positioner is removed when the examination arm is at 33 degrees and, th

FDAJul 1, 2008AL, CA, CO +16 more• GE Healthcare

GE Healthcare Integrated IT Solutions: GE Healthcare Centricity Perinatal (formerly QS) System -...

Patient information mix-up: When the PFILS application, configured with a backup server has experienced a network interruption, PFILS verify could result in the Centricity Perinatal application recording non-identifiable patient information to the incorrect patient file.

FDAJun 30, 2008PR• GE Healthcare Integrated IT Solutions

Philips Medical Systems North America Co. Phillips: Motorized Height Ceiling Suspensions (MCS) and motorized ...

Monitor ceiling carriage may separate from the monitor ceiling suspension.

FDAJun 26, 2008Nationwide• Philips Medical Systems North America Co. Phillips

Cardinal Health: Corflo Anti-I.V. NG Tube for Pediatric and Neonatal Use; ...

The male Luer adapter may be the wrong component therefore the feeding set would not be able to be connected to the tube nor would the cap fit securely.

FDAJun 25, 2008CA, IL, KY +1 more• Cardinal Health

GE Healthcare: Advantx-E The Advantx imaging system is intended to be u...

GE Healthcare has become aware of 2 potential conditions that could occur with the MAVIG GD Monitor Suspension that is used with Advantx-E, Innova 2000, 21000IQ, 3100/3100IQ, 4100/4100IQ and 2121 IQ/3131IQ cardiovascular systems. The two conditions include 1). Due to insufficient securing of the connecting elements, the LCD vertical monitor support may disengage from its arm and fall on the tab

FDAJun 24, 2008AL, AZ, AR +45 more• GE Healthcare

The recall involves motors included with lawn sprinkler pumps and jet pumps manufactured by F. E. Myers Co. The recall also includes replacement pump motors that were sold separately. Model Number Product Description QP10 Lawn Sprinkler Pump QP10B Lawn Sprinkler Pump with Brass Impeller HJ100S Shallow Well Jet Pump HJ100S-1 Shallow Well Jet Pump with Brass Impeller HJ100D Deep Well Jet Pump HJ100D-LR Deep Well Jet Pump Less Regulator HJ100D-1 Deep Well Jet Pump with Brass Impeller 20935A000K Individually Sold Replacement Motor Only pumps manufactured between August 2007 and May 2008 are included in the recall. The pump's model number, manufacturing date code and the name "Myers" can be located on the pump's nameplate and packaging. The pump's motor has "A. O. Smith" and model number "C48D52B86" on the motor's nameplate. The replacement motor's packaging has "Myers" and model number "20935A000K" printed on it. Products with an "OK" sticker on the product or packaging are not included in the recall.

CPSCJun 24, 2008Nationwide• A.O. Smith Electrical Products Co., of Tipp City, Ohio