FDA recall record

Aesculap Implant Systems ENNOVATE MIS REMOVALKEY SHORT, product code SZ380R recall — FDA Z-1428-2022

Fracture or breakage of the spinal fixation arm at the downtube instrument if the 90 degree angle is not met when using the removal key with the spinal…

Class IIclassification
Z-1428-2022official record ID
Jul 27, 2022report date

Recall record at a glance

Official recordZ-1428-2022
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmAesculap Implant Systems LLC
Report dateJul 27, 2022
Recall initiation dateJul 13, 2020
Quantity16
LocationCenter Valley, PA, United States

Official product description

ENNOVATE MIS REMOVALKEY SHORT, product code SZ380R

Why the product was recalled

Fracture or breakage of the spinal fixation arm at the downtube instrument if the 90 degree angle is not met when using the removal key with the spinal fixation system.

Distribution information

United States Nationwide distribution in the states of CA, CO, IL, MI, OH & TX.

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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