FDA recall record

RM Temena GmbH Ultrasound USB needles, with 30 degree bevel, packaged individually, 10 recall — FDA Z-1609-2014

Ultrasound needles may be defective and leak at the needle hub.

Class IIclassification
Z-1609-2014official record ID
May 21, 2014report date

Recall record at a glance

Official recordZ-1609-2014
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmRM Temena GmbH
Report dateMay 21, 2014
Recall initiation dateMar 19, 2014
Quantity7370 needles
LocationFelsberg, Germany

Official product description

Ultrasound USB needles, with 30 degree bevel, packaged individually, 10 needles/box, item number REF USB050-22. Needles for peripheral nerve blocking under ultrasound guidance

Why the product was recalled

Ultrasound needles may be defective and leak at the needle hub.

Distribution information

US Distribution including the states of MD and IL.

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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