FDA recall record

Osteomed REF 218-1604-SP-10, Profile 0 4mm AutoDrive Screw Sterile Qty 10, Rx Only, Sterile recall — FDA Z-2108-2023

Screws for osteotomies have contain an undersize screwhead which has the potential to pass through the plate hole.

Class IIclassification
Z-2108-2023official record ID
Jul 19, 2023report date

Recall record at a glance

Official recordZ-2108-2023
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmOsteomed, LLC
Report dateJul 19, 2023
Recall initiation dateMay 31, 2023
QuantityN/A
LocationAddison, TX, United States

Official product description

REF 218-1604-SP-10, Profile 0 4mm AutoDrive Screw Sterile Qty 10, Rx Only, Sterile

Why the product was recalled

Screws for osteotomies have contain an undersize screwhead which has the potential to pass through the plate hole.

Distribution information

Worldwide - US Nationwide distribution in the states of AZ, CA, FL, GA, KS, KY, MD, MO, MT, NE, NY, TN, TX and the country of SG.

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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