FDA recall record

The Anspach Effort 16cm Minimally Invasive Attachment recall — FDA Z-1037-2015

Customer complaint indicating the color bands on the MIA16-G1 were not correct.

Class IIclassification
Z-1037-2015official record ID
Feb 11, 2015report date

Recall record at a glance

Official recordZ-1037-2015
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmThe Anspach Effort, Inc.
Report dateFeb 11, 2015
Recall initiation dateDec 10, 2014
Quantity8
LocationPalm Beach Gardens, FL, United States

Official product description

16cm Minimally Invasive Attachment. For use with Motor Systems for cutting and shaping bones, including the spine and cranium. Model MIA16-G1

Why the product was recalled

Customer complaint indicating the color bands on the MIA16-G1 were not correct.

Distribution information

US Distribution to the states of: NC and CA., and Internationally to Switzerland.

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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