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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

Newport Corp: Laser Systems and Power Supplies Recalled Due to Safety Interlock Failure

Agency Publication Date: June 5, 2024
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Summary

Newport Corp is recalling 19 laser system components, specifically the N-LHP-928(j) laser head sets and N5-LPL-944-080 or N6-LPL-944-080 power supplies. These Class IIIb or IV laser products were designed with a key-actuated master control that is meant to disable the laser when the key is removed. However, a defect allows the laser to remain operational even after the key has been removed, violating federal safety standards. Consumers should contact Newport Corp immediately for guidance on how to secure their equipment.

Risk

The failure of the key-switch to disable the laser when the key is removed poses a significant safety risk, as unauthorized or accidental activation of high-power lasers can lead to severe eye injuries or skin burns. Because the laser remains 'on' without the master key, there is no physical lockout to prevent dangerous exposure.

What You Should Do

  1. Check your laser equipment to see if it matches the affected model numbers: N-LHP-928(j) (sold as a set), N5-LPL-944-080 (power supply), or N6-LPL-944-080 (power supply).
  2. Verify your serial numbers against the affected list: for the N-LHP-928 set, look for 6905AE, 6907AE, 9023AE, 3148AF, 6899AE, 6909AE, 9025AE, 5695AF, 5696AF, 5691AF, 5692AF, 5693AF, or 5694AF; for the N6-LPL-944-080 power supply, look for 23060081 or 23060079.
  3. Ensure the laser is powered down and manually disconnected from its power source when not in use, as the key removal alone will not turn the device off.
  4. Contact Newport Corp directly to arrange for a repair or corrective action for your unit.
  5. Contact your healthcare provider or Newport Corp for further instructions regarding device safety and potential remedy options.
  6. For additional questions, contact the FDA at 1-888-463-6332 or visit www.fda.gov/medical-devices/medical-device-recalls.

Your Remedy Options

๐Ÿ“‹Other Action

Manufacturer correction/repair

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

Affected Products

Product: Newport N-LHP-928(j) Laser Head/Power Supply Set
Model / REF:
N-LHP-928(j)
Lot Numbers:
6905AE
6907AE
9023AE
3148AF
6899AE
6909AE
9025AE
5695AF
5696AF
5691AF
5692AF
5693AF
5694AF
Product: Newport N5-LPL-944-080 Power Supply
Model / REF:
N5-LPL-944-080
Product: Newport N6-LPL-944-080 Power Supply
Model / REF:
N6-LPL-944-080
Lot Numbers:
23060081
23060079

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 94748
Status: Active
Manufacturer: Newport Corp
Sold By: Newport Corp
Manufactured In: United States
Units Affected: 19
Distributed To: Nationwide

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.

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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.