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LMS Medical Systems Ltd

LMS Medical Systems Ltd Recalls

All product recalls associated with LMS Medical Systems Ltd.

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Recall Summary

Total Recalls

1000

Past Year

898

Class I (Serious)

125

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 16781–16800 of 17592 recalls

LMS Medical Systems Ltd: CALM software, version 02.09.01 This software is intend...

A deficiency in the software code can, in certain circumstances, cause data for the wrong patient to be displayed in the Tracing Review screen when a user is acknowledging an Alert

FDAJan 11, 2005AL, IL, MD +2 more• LMS Medical Systems Ltd

Spacelabs Medical Incorporated: Ultraview Universal Clinical Workstation System Model 90385.

Weakness of the swivel base for the universal clinical workstation may result in the unit falling from its mounted position endangering users and patients.

FDAJan 7, 2005IN, OR• Spacelabs Medical Incorporated

Smiths Medical PM, Inc.: Advisor Vital Signs Monitor model 9200, catalog number 92...

An issue with the pace detect function was discovered on a 9200 II monitor. Could result in a falsely high or low heart rate reading.

FDA

1...838 839840841 842...880

Page 840 of 880Next

Jan 5, 2005

Nationwide

• Smiths Medical PM, Inc.

Northwest Medical Physics Equipment Inc: ISOLOC Software Version 6.0, Part Number NT-NW-425-520. ...

When ISOLOC version 6.0 software was used in the Anatomic Landmark mode, the couch moves display in the Couch Translator window was incorrect.

FDADec 30, 2004Nationwide• Northwest Medical Physics Equipment Inc

General Electric Med Systems LLC: Precision 500D Radiographic/Fluoroscopic X-ray System, mo...

Units have a defect in accordance with 21 CFR 1003.2 because an incorrect exposure can occur.

FDADec 30, 2004Nationwide• General Electric Med Systems LLC

General Electric Med Systems LLC: Proteus XR/a Radiographic X-ray System, models 2259973-1,...

Units have a defect in accordance with 21 CFR 1003.2 because an incorrect exposure can occur.

FDADec 30, 2004Nationwide• General Electric Med Systems LLC

Gas Control Valve (Robertshaw) – Potential Malfunction (2004)

Fire/Burn Risk

The 7000 Series Gas Valves that are being recalled are installed in gas appliances, including residential space heaters, wall heaters, boilers, fireplaces, pool heaters, infrared heaters and furnaces, and commercial heating applications such as commercial cooking appliances, fryers, commercial water heaters, and poultry brooders. The recalled valves were manufactured between February 2003 and September 2004 and have production dates beginning with code 0306 and ending with 0436. However, not all 7000 Series valves manufactured during the indicated timeframe are being recalled. Of particular note are model numbers containing the letters "MV." Recalled gas valves include "MV" models that also include the letters "LP" and model numbers 7000AMV; 7000BMV; 7000BMV-S7CL; 7000MVLC; and 7000MVRCLC. All "MV" valves with the indicated date codes that have been converted to Liquid Propane (LP) gas use are also included in the recall. NOT included in the recall are model numbers 7010 and above; model numbers containing the letters "D" or "BV;" and model numbers containing the letters "MV", except for the ones listed above.

CPSCDec 22, 2004Nationwide• Robertshaw Controls Company of Long Beach, Calif.

Philips Medical Systems Sales & Service Region No. America: Xcelera R1.2 Cardiology image and information management ...

Loss of image data from image repository and archive requiring patients to undergo repeat imaging.

FDADec 21, 2004Nationwide• Philips Medical Systems Sales & Service Region No. America

Metallic Children's Necklaces (Raymond Geddes) – Choking Risk (2004)

Laceration Risk

The recalled necklaces have medallions that came in four different designs, depicting frogs, dolphins with a small bead on the tail, a sunshine smiley face and an alien face on a starburst. The medallion is on a black rope chain surrounded by a metallic bead with a coil section.

CPSCDec 17, 2004Nationwide• Raymond Geddes Co. Inc., of Baltimore, Md.

Beckman Coulter Inc: COULTER LH 750 Hematology Analyzer.

A rare risk of sample misidentification exists with Coulter LH 750 Hematology Analyzers. The printout results from the instrument are affected; however, the results stored in the workstation's database are not affected.

FDADec 16, 2004Nationwide• Beckman Coulter Inc

Philips Medical Systems: Philips Heartstart MRx Monitor/Defibrillator Models: M35...

In Software versions below A.02.00, with the sync function enabled and the device switched from manual to AED, there may be an unexpected delay in delivery of energy

FDADec 15, 2004Nationwide• Philips Medical Systems