FDA recall record

Pro-Dex KLS martin Group KLS E-COUPLING ADAPTER REF PDEC-1000-2 E-Coupling Adapter Assembly recall — FDA Z-1391-2023

Incorrect Unique Device Identifier/GTIN code was used on product.

Class IIclassification
Z-1391-2023official record ID
Apr 26, 2023report date

Recall record at a glance

Official recordZ-1391-2023
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmPro-Dex Inc.
Report dateApr 26, 2023
Recall initiation dateFeb 14, 2023
Quantity199 devices
LocationIrvine, CA, United States

Official product description

KLS martin Group KLS E-COUPLING ADAPTER REF PDEC-1000-2 E-Coupling Adapter Assembly used to connect the KLS driver (e.g. drill) to a driver bit that fits into the adapter.

Why the product was recalled

Incorrect Unique Device Identifier/GTIN code was used on product.

Distribution information

U.S. Nationwide distribution in the state of FL.

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: 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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