FDA recall record

Siemens Medical Solutions USA Uroskop Omnia Max -fluoroscopic X-ray system Model # 10762473 recall — FDA Z-0985-2019

The swivel arm holding the monitors may become dislodged from the carrying arm.

Class IIclassification
Z-0985-2019official record ID
Mar 13, 2019report date

Recall record at a glance

Official recordZ-0985-2019
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmSiemens Medical Solutions USA, Inc.
Report dateMar 13, 2019
Recall initiation dateFeb 8, 2019
Quantity191
LocationMalvern, PA, United States

Official product description

Uroskop Omnia Max -fluoroscopic X-ray system Model # 10762473 Uroskop Omnia Max is a device intended to visualize anatomical structures by converting an X-ray pattern into a visible image.

Why the product was recalled

The swivel arm holding the monitors may become dislodged from the carrying arm.

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: 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

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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