FDA recall record

Roche Diagnostics cobas p 701 post-analytical units, Part Number 05349966001 recall — FDA Z-1928-2019

There is a potential for the tray input flap on the post analytical units to become loose, potentially detaching from the instrument.

Class IIIclassification
Z-1928-2019official record ID
Jul 10, 2019report date

Recall record at a glance

Official recordZ-1928-2019
CategoryMedical Device Recalls
ClassificationClass III
FDA record statusTerminated
Recalling firmRoche Diagnostics Corporation
Report dateJul 10, 2019
Recall initiation dateApr 4, 2019
Quantity9 units
LocationIndianapolis, IN, United States

Official product description

cobas p 701 post-analytical units, Part Number 05349966001. For diagnostic sample storage and retrieval.

Why the product was recalled

There is a potential for the tray input flap on the post analytical units to become loose, potentially detaching from the instrument.

Distribution information

US Nationwide Distribution in the states of AL, CA, FL, IA, IL, KY, MD, OR & PA

How to read the classification

FDA Class III generally covers situations in which use of or exposure to the product is not likely to cause adverse health consequences. The classification displayed here is taken from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

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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