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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Medium RiskFDA Device
Medical Devices/Surgical Equipment

DKK Dai-Ichi Shomei Co., Ltd.: LFS Flat Screen Arm Systems Recalled Due to Risk of Falling Monitors

Agency Publication Date: October 6, 2023
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Summary

DKK Dai-Ichi Shomei Co., Ltd. has recalled approximately 1,467 LFS Flat Screen Arm Systems, including those paired with surgical lamps and standalone support arms. The recall affects Aurora series, Aurora 2, 3, 4, Aurora Astro, Stellar XL, and Stellar series used in medical environments. These devices have a defective or missing stopper block that allows the screen to rotate too far, putting excessive stress on the spring shaft which can cause it to break and shear off. This could result in the heavy flat screen monitor falling unexpectedly.

Risk

A broken or missing stopper block allows the monitor to rotate beyond its safe limit, causing the internal spring shaft to snap under pressure. This mechanism of failure can cause the flat screen monitor to detach and fall, posing a serious risk of impact injury to patients or medical staff during procedures.

What You Should Do

  1. Check your surgical lamp or flat screen arm system for model series Aurora (series 1-4, Astro) or Stellar (XL and standard) to see if it uses the LFS arm system.
  2. Identify your device's specific serial number and model number. For systems with surgical lamps, check for model numbers like LFSST2323, LFSST29TV23, and others in the LFSST or LFSLED series against the provided serial number list (ranging from 06087323 to BM008127).
  3. For standalone support arms without lamps, check for serial numbers including those starting with RA (e.g., RA000006 to RA001732) and BM (e.g., BM003066 to BM029673).
  4. Contact your healthcare facility's maintenance department or the manufacturer, DKK Dai-Ichi Shomei, to verify if your specific unit is affected by the broken or missing stopper block defect.
  5. If you confirm your device is affected, contact the manufacturer for further instructions regarding a repair or potential replacement to secure the monitor arm.
  6. Contact the FDA at 1-888-463-6332 if you have additional safety questions or wish to report an incident related to this equipment.

Your Remedy Options

๐Ÿ“‹Other Action

Professional evaluation and adjustment

How to: Contact your healthcare provider or the manufacturer for further instructions and potential refund

Affected Products

Product: LFS Flat screen arm system with surgical lamp (Models: Aurora series, Aurora 2 series, Aurora 3 series, Aurora 4 series, Aurora Astro series, Stellar XL, and Stellar series)
Model / REF:
LFSST2323
LFSLFSST29TV23
LFSST29TV23
LFSST23TV
LFSST23
LFSST2323TV
LFSLFSST2323
LDFSLFSLED7TV5
LDFSLFSLED7TV55
LFSLED55
LFSLFSST23
LFSST2923TV
LFSST29TV
LFSST29
LFSST19WC
LFSST2923
LFSLFSST-1
LFSST292323
LFSST1919WC
LFS ST2319WC
Lot Numbers (92):
06087323 - 06087352
06087353 - 06087354
06081292 - 06081293
06087448 - 06087449
06087450 - 06087469
06097595 - 06097596
06107716 - 06107718
06107719 - 06107728
06107730
06107731 - 06107732
06111348 - 06111349
06117855 - 06117856
06117857 - 06117866
06117868 - 06117868
06111350 - 06111351
06117949 - 06117949
06117954 - 06117973
06118031 - 06118032
06128116 - 06128131
06128172 - 06128176
06128177 - 06128186
06128187 - 06128188
07010004
07010002
07010005 - 07010006
07028436 - 07028441
07030080 - 07030081
07048491 - 07048495
07058506 - 07058507
07058508 - 07058512
07068602 - 07068604
07068605 - 07068607
07068611 - 07068622
07068609 - 07068610
07068667 - 07068670
07061479 - 07061484
07078679 - 07078680
07071485 - 07071488
07071501
07088741 - 07088742
07081124
07088766
07098769 - 07098773
07098767 - 07098768
07098774 - 07098775
07108885 - 07108889
07108883 - 07108884
07108876 - 07108882
07108890 - 07108891
07101533 - 07101534
Product: LFS Flat screen support arm systems without surgical lamp (Models: Aurora series, Aurora 2 series, Aurora 3 series, Aurora 4 series, Aurora Astro series, Stellar XL, and Stellar series)
Model / REF:
LFS Flat Screen Support Arm Model Numbers
Lot Numbers:
RA000006 to RA001732 (See description for full serial list)
BM003066 to BM029673 (See description for full serial list)

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 92999
Status: Active
Manufacturer: DKK Dai-Ichi Shomei Co., Ltd.
Sold By: Authorized medical equipment distributors
Manufactured In: Japan
Units Affected: 2 products (256 units; 1211 units)
Distributed To: Michigan

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.