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Open, Classified

Centurion OB INSTRUMENT TRAY, REF MN3925; Medical procedure convenience tray

FDA Recall Z-1917-2024 · Posted 2024-05-29

Recall StatusOpen, Classified
Product CodeLRP
Date Initiated2024-03-01
Product Quantity30 units

Reason for Recall

Trumpet Needle Guide ring can detach when excessive pressure is applied.

Firm Action

Medline issued a correction notice to its consignees on 03/01/2024 via email and USPS first class mail. The notice explained the issue and requested the consignee identify and quarantine all affected products, and respond to the notice. Once the response was received Medline would provide labels to place over the affected product in stock. If the product was further distributed the party which distributed the product was directed to notify their customers.

Root Cause

Process control

Distribution Pattern

US Nationwide distribution.

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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