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Open, Classified

YelloPort Elite, REF: EO0509505, 5x95 Optical Trocar, Rx Only, SterileR

FDA Recall Z-1602-2023 · Posted 2023-05-17

Recall StatusOpen, Classified
Product CodeGCJ
Date Initiated2023-03-28
Product Quantity3405 units

Reason for Recall

Optical Trocars sterility assurance can not be guaranteed

Firm Action

On March 29, 2023, Surgical Innovations issued a "Urgent Field Safety Notice" to affected consignees via E-Mail. An update to the communication was sent on 4/17/2023 to affected consignees via E-Mail. In addition to informing consignees about the recall, Surgical Innovations ask consignees to take the following action: 1. Distributor should confirm receipt of this Field Safety Notice 2. Identify the devices held in stock at the distributor and quarantine affected batches awaiting further instruction. 3. Issue this Field Safety Notice to all end users (Hospital) that the distributor has supplied 4. All product still in stock at the end users must be returned to the distributor. 5. Confirmation must be obtained by the distributor that either all stock has been returned or that any other product has been successfully used. 6. Confirmation to Surgical Innovations using the attached form of this disposition of all stock 7. Await further instruction from Surgical Innovations regarding further action for the affected products.

Root Cause

Other

Distribution Pattern

US: MA OUS: None

Related FDA 510(k) Records

Devices referenced by this recall via K-numbers.

Official Source

View FDA Recall →

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

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