NeoProbe Gamma Detection Device (2019-03-17)

Starting date:

March 17, 2019

Posting date:

April 29, 2019

Type of communication:

Medical Device Recall

Subcategory:

Medical Device

Hazard classification:

Type III

Source of recall:

Health Canada

Issue:

Medical Devices

Audience:

General Public, Healthcare Professionals, Hospitals

Identification number:

RA-69774

Last updated: 2019-04-30

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  Reason
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  Affected products

Affected Products

NeoProbe Gamma Detection Device

Reason

NeoProbe bluetooth 14 mm reusable probe, straight secondary packaging has FCC ID, IC and ANATEL numbers that are incorrect for the current bluetooth modules used in the devices. The primary device label is correct.

Affected products