Health product recall

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

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

NeoProbe Gamma Detection Device

Lot or serial number

1100-003385

Model or catalog number

NPB14S

Companies
Manufacturer

Devicor Medical Products Inc.

300 E-Business Way, Fifth Floor

Cincinnati

45241

Ohio

UNITED STATES