FDA recall record

Waldemar Link GmbH & Co. KG Embrace Drill Tower, Standard/Lateral (25mm) recall — FDA Z-1258-2024

The surgical techniques for the Embrace Shoulder Instruments -Drill Tower (Article REF 645-081/62 & /63) have mixed-up type descriptions ("standard" vs…

Class IIclassification
Z-1258-2024official record ID
Mar 13, 2024report date

Recall record at a glance

Official recordZ-1258-2024
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmWaldemar Link GmbH & Co. KG (Mfg Site)
Report dateMar 13, 2024
Recall initiation dateJan 29, 2024
Quantity6 units
LocationNorderstedt, Germany

Official product description

Embrace Drill Tower, Standard/Lateral (25mm)

Why the product was recalled

The surgical techniques for the Embrace Shoulder Instruments -Drill Tower (Article REF 645-081/62 & /63) have mixed-up type descriptions ("standard" vs "wedged") in the overview of the instruments.

Distribution information

US Nationwide distribution in the states of AL and LA.

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: E-Mail.

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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