FDA recall record

Stryker GmbH Guide Wire with Ruler Tube 3x1000 mm DIA recall — FDA Z-1621-2025

The metal ring at the end of the Guide Wire with Ruler Tube may detach from the main body of the instrument during use in surgery.

Class IIclassification
Z-1621-2025official record ID
Apr 23, 2025report date

Recall record at a glance

Official recordZ-1621-2025
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmStryker GmbH
Report dateApr 23, 2025
Recall initiation dateMar 28, 2025
Quantity6407 units
LocationSelzach, Switzerland

Official product description

Guide Wire with Ruler Tube 3x1000 mm DIA; Catalog number/REF: 2351-3100S;

Why the product was recalled

The metal ring at the end of the Guide Wire with Ruler Tube may detach from the main body of the instrument during use in surgery.

Distribution information

US Nationwide distribution in the states of CA, GA, IL, KY, MA, MD, NY, OH, TN, TX, WV.

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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