FDA recall record

MicroAire Surgical Instruments SST TWIST DRILL, STANDARD, 1.6mm Dia. x 127mm, REF 8054-010 recall — FDA Z-0412-2018

One lot was found to contain both the correct twist drill (1.6mm) as well as an incorrect twist drill (2.0mm)

Class IIclassification
Z-0412-2018official record ID
Feb 7, 2018report date

Recall record at a glance

Official recordZ-0412-2018
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmMicroAire Surgical Instruments, LLC
Report dateFeb 7, 2018
Recall initiation dateMay 22, 2017
Quantity42
LocationCharlottesville, VA, United States

Official product description

SST TWIST DRILL, STANDARD, 1.6mm Dia. x 127mm, REF 8054-010, STERILE This product line is intended for use in orthopaedic surgery (large and small bone surgeries) to cut bone

Why the product was recalled

One lot was found to contain both the correct twist drill (1.6mm) as well as an incorrect twist drill (2.0mm)

Distribution information

US Distribution.

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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