CLASS II Device recall · Reported 20 Sep 2023 · FDA Enforcement Report
nanoDot kit (contains nanoDot A, B, C) recalled by Landauer
Landauer is recalling nanoDot kit (contains nanoDot A, B, C). The recall was initiated on 12 Jul 2023 and the FDA has classified it as Class II.
Check your package
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
Recall details
- Recall number
- Z-2553-2023
- FDA event ID
- 92647
- Recalling firm
- Landauer, Glenwood, IL
- Classification
- Class II
- Status
- Completed
- Recall initiated
- 12 Jul 2023
- FDA classified
- 12 Sep 2023
- Reported
- 20 Sep 2023
- Type
- Voluntary: Firm initiated
- Customers notified by
- Letter
- Reason category
- Other Reasons
- Device type
- Patient Monitors
Timeline
| 12 Jul 2023 | Recall initiated by company | |
| 12 Sep 2023 | Classified by FDA | +62 days |
| 20 Sep 2023 | Published in enforcement report | +8 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
LANDAUER received reports indicating that some nanoDots may potentially be outside of the specified range of +/-5.5% accuracy. Investigation of nanoDots indicated the presence of a potential non-conformance in the Optical Stimulated Luminescence (OSL) material that is beamed after exposure and emits fluorescence proportional to radiation exposure.
Product as listed by the FDA
nanoDot kit (contains nanoDot A, B, C), Model Number 03500-000; radiation monitoring dosimeter used with the microSTAR readers
Where it was distributed
Worldwide
Questions about this recall
Why was it recalled?
LANDAUER received reports indicating that some nanoDots may potentially be outside of the specified range of +/-5.5% accuracy. Investigation of nanoDots indicated the presence of a potential non-conformance in the Optical Stimulated Luminescence (OSL) material that is beamed after exposure and emits fluorescence proportional to radiation exposure.
Which lots are affected?
UDI/DI 0860003399903, all batch numbers
Where was it sold?
Worldwide
What should I do if I have it?
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
What does Class II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
Other products in this recall event
37 other products · FDA event 92647This product is part of a recall event; the main page for the event is nanoDot D2DNS recalled by Landauer.
More recalls from Landauer
All 40| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Device | CLASS II | microStar Reader recalled by Landauer | Landauer | Device Malfunction | Nationwide |
| Device | CLASS II | microSTARii reader, Medical Dosimetry System recalled by Landauer | Landauer | Device Malfunction | IL |
| Device | CLASS II | NanoDots, Model Numbers: a) BC30023, description: QC Set recalled | Landauer | Packaging Defects | IL |
| Device | CLASS II | nanoDot D2DNN recalled by Landauer | Landauer | Other | IL |
| Device | CLASS II | Calibrate (80 kVp) nanoDot D2DNS recalled by Landauer | Landauer | Other | IL |
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| Device | CLASS II | Lux-Dx, Lux-Dx II, Lux-Dx II+ Insertable Cardiac Monitor recalled | Boston Scientific | Device Malfunction | Nationwide |
| Device | CLASS II | Lux-Dx, Lux-Dx II, Lux-Dx II+ Insertable Cardiac Monitor recalled | Boston Scientific | Device Malfunction | Nationwide |
| Device | CLASS II | IQecg Digital ECG recalled by Midmark | Midmark | Labeling Errors | Nationwide |