FDA recall record

Blue Ortho Instructions For Use document of the GPS Trackers recall — FDA Z-0288-2021

Appropriateness of the language used in the Tracker reprocessing instruction. Reason is that some Low Temperature sterilization conditions mentioned in…

Class IIclassification
Z-0288-2021official record ID
Nov 4, 2020report date

Recall record at a glance

Official recordZ-0288-2021
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmBlue Ortho
Report dateNov 4, 2020
Recall initiation dateSep 10, 2020
Quantity3471 units
LocationGieres, N/A, France

Official product description

Instructions For Use document of the GPS Trackers.

Why the product was recalled

Appropriateness of the language used in the Tracker reprocessing instruction. Reason is that some Low Temperature sterilization conditions mentioned in the IFUs are approved based on rational documents.

Distribution information

Domestic Distribution Only: CA, CO, SC and WI.

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: E-Mail.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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