FDA recall record

Oakworks Ultrasound EA (Ergonomic Advantage) table version recall — FDA Z-0730-2024

Backrest platform stress fracture - the table is not operational in an inclined position

Class IIclassification
Z-0730-2024official record ID
Jan 24, 2024report date

Recall record at a glance

Official recordZ-0730-2024
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmOakworks Inc.
Report dateJan 24, 2024
Recall initiation dateDec 5, 2023
Quantity28 units
LocationNew Freedom, PA, United States

Official product description

Ultrasound EA (Ergonomic Advantage) table version; V2 (Vascular 2 Section) Echocardiography -An Ultrasound examination table

Why the product was recalled

Backrest platform stress fracture - the table is not operational in an inclined position

Distribution information

US Nationwide 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: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit.

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

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

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