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Use caution Medical device recall · FDA · Published October 27, 2017

L3 Security & Detection X-ray System Recall: Air Gap Risk in Airport Baggage Scanners

L3 Security & Detection recalls Examiner 3DX 6:000 airport baggage x-ray systems due to potential x-ray leakage from gaps in shielding, exceeding federal safety limits.

🇺🇸 FDA recall #Z-0270-2018Medical deviceL3 Security & Detection ›
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Recalling firmL3 Security & Detection10E Commerce Way · Woburn, MA 01801-1044
✎ GovInfoNow plain-language explainer

What happened, in plain English

L3 Security & Detection is recalling its Examiner 3DX 6000 airport baggage x-ray systems because gaps in the x-ray shielding can cause x-ray emissions to exceed federal safety limits. This could lead to unnecessary radiation exposure for people near the scanner. Read more at govinfonow.com/recall/72652-l3-security-detection-x-ray-system-recall-air-gap-risk.

Source Summary by GovInfoNow · govinfonow.com/recall/72652-l3-security-detection-x-ray-system-recall-air-gap-risk · Updated September 14, 2026 · FDA enforcement record: FDA #Z-0270-2018

Cite this page

“L3 Security & Detection X-ray System Recall: Air Gap Risk in Airport Baggage Scanners.” GovInfoNow, updated September 14, 2026. https://govinfonow.com/recall/72652-l3-security-detection-x-ray-system-recall-air-gap-risk. Based on FDA recall #Z-0270-2018 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0270-2018%22&limit=1).

Why it’s dangerous

In airport settings, gaps can form where tunnel entrances/exits meet the main x-ray scanner tunnel. This gap in x-ray shielding allows radiation emissions to exceed federal safety limits, potentially exposing people to unnecessary radiation.

Who’s affected

Airports using the Examiner 3DX 6000 x-ray systems for checked baggage screening are affected. Staff and passengers near the scanner may be at risk if x-ray leakage occurs.

How to tell if you have this one

Check for the Examiner 3DX 6000 model number on the system. These systems were sold at airports for security screening of checked airline baggage.

  • Brand
    L3 Security & Detection
  • Category
    Medical device
Based on the official FDA remedy

What to do — step by step

  1. Check for Air Gap

    Inspect the x-ray scanner for gaps where tunnel entrances or exits meet the main scanner tunnel.

  2. Contact L3 for Guidance

    Reach out to L3 Security & Detection for specific instructions on addressing potential gaps in shielding.

Where it went and when

Where it was distributed

Distributed nationwide.

Alaska: yesAKMaine: yesMEVermont: yesVTNew Hampshire: yesNHWashington: yesWAIdaho: yesIDMontana: yesMTNorth Dakota: yesNDMinnesota: yesMNIllinois: yesILWisconsin: yesWIMichigan: yesMINew York: yesNYRhode Island: yesRIMassachusetts: yesMAOregon: yesORNevada: yesNVWyoming: yesWYSouth Dakota: yesSDIowa: yesIAIndiana: yesINOhio: yesOHPennsylvania: yesPANew Jersey: yesNJConnecticut: yesCTCalifornia: yesCAUtah: yesUTColorado: yesCONebraska: yesNEMissouri: yesMOKentucky: yesKYWest Virginia: yesWVVirginia: yesVAMaryland: yesMDDelaware: yesDEArizona: yesAZNew Mexico: yesNMKansas: yesKSArkansas: yesARTennessee: yesTNNorth Carolina: yesNCSouth Carolina: yesSCDistrict of Columbia: yesDCOklahoma: yesOKLouisiana: yesLAMississippi: yesMSAlabama: yesALGeorgia: yesGAHawaii: yesHITexas: yesTXFlorida: yesFL

FDA distribution: “USA (nationwide) Distribution.  Owned and operated by the U.S. Transportation Security Administration. Location of individual products is law enforcement sensitive. TSA HQ is located in Crystal City, Virginia.” States read from FDA’s own wording; “not listed” means the notice does not name it.

Distributed nationwide.

Recall timeline

FDA terminated this recall 2.3 years after the firm started it.

1. Firm started the recall: Oct 27, 201712. FDA classified it Class II: Dec 22, 201723. Published in FDA’s Enforcement Report: Jan 3, 201834. FDA terminated the recall: Feb 10, 2020420172020
  1. Firm started the recall
  2. FDA classified it Class II
  3. Published in FDA’s Enforcement Report
  4. FDA terminated the recall

Dates from the agency record only; steps without a date are left out.

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Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

  • Official source: FDA Recall #Z-0270-2018 (October 27, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0270-2018 to see it in context.
  • Plain-language summary written by qwen3:4b on September 14, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
  • GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA