Recall Z-1601-2023

Surgical Innovations Ltd · initiated March 28, 2023

Class II Open, Classified

Class II – products that might cause a temporary health problem or pose a slight threat of a serious nature

Product

YelloPort Elite, REF: EO0507005, 5x70 Optical Trocar, , Rx Only, SterileR

Codes / lots: Lot # 738182 ; UDI-DI: (01) 05051986013398

Reason for recall

Optical Trocars sterility assurance can not be guaranteed

FDA-determined cause: Other

Action taken

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.

Details

Recall number
Z-1601-2023
Initiated
March 28, 2023
Posted by FDA
May 17, 2023
Product code
GCJ – Laparoscope, General & Plastic Surgery
Quantity
2380 units
Distribution
US: MA OUS: None
Recalling firm
Surgical Innovations Ltd, Leeds

Official FDA recall record

Other products in the same recall event

RecallProductInitiated
Z-1602-2023 Class IIYelloPort Elite, REF: EO0509505, 5x95 Optical Trocar, Rx Only, SterileROptical Trocars sterility assurance can not be guaranteed 03/28/2023Open, Classified