Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-1382-2024 — GeoMed Custom Tracecarts, REF Numbers: a) 53-1831 ORTHO TOTAL JOINT TRACECART, b) 53-1836 GENERAL SURGERY TRACECART

U.S. FDA — Device Enforcement · United States · 2024-02-13 · Class I

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1382-2024
Date of alert
2024-02-13
Country / jurisdiction
United States
Risk level
Class I
Risk type
recall
Brand
DeRoyal Industries Inc
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
0749756598088
Reported risk: DeRoyal manufactured and distributed Surgical Tracecarts that contain a Nurse Assist 16FR Silver Urine Meter Foley which were subsequently recalled.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

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