Recall Z-1620-2025— Stryker GmbH
Class II · Ongoing
Class II FDA medical device recall by Stryker GmbH, initiated 2025-03-28. FDA's recall record names no specific 510(k) clearance for this event. Product: Guide Wire with Ruler Tube 3x800 mm DIA; Catalog number/REF: 2351-3080S;. Reason: 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..
- Recalling firm
- Stryker GmbH
- Classification
- Class II
- Status
- Ongoing
- Initiated
- 2025-03-28
- Firm location
- Selzach, Switzerland
Product description
Guide Wire with Ruler Tube 3x800 mm DIA; Catalog number/REF: 2351-3080S;
Reason for recall
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.
Data sourced from openFDA. This site is unofficial and independent of the FDA.