Z-0287-2008

Ellex Integre Duo, Model No: LP1RG - Ellex Medical PTY, LTD 82 Gilbert Street, Adelaide, S.A. 5000...

Name: Z-0287-2008 Ellex Integre Duo, Model No: LP1RG - Ellex Medical PTY, LTD 82 Gilbert Street, Adelaide, S.A. 5000...
Creator: Ellex USA
Published: 2007-06-13
License: https://open.fda.gov/license/

Ellex USA / initiated 2007-06-13 / Terminated / root cause: design

FDA source

Ellex USA began a recall of Ellex Integre Duo, Model No: LP1RG - Ellex Medical PTY, LTD 82 Gilbert Street, Adelaide, S.A. 5000, AUSTRALIA. (The Integre Duo is a dual-wavelength surgical... on 2007-06-13. The reason FDA records is "Electric Shock from Power Supply: The power supply has a defect which can cause an electrical shock to user". As of 2026-09-10, the recall status on record is Terminated, and MDM tags the root cause as design.

Recall record

Recall number: Z-0287-2008
Status: Terminated
Initiated: 2007-06-13
Posted: 2007-12-20
Terminated: 2008-10-17
Recalling firm: Ellex USA
Product: Ellex Integre Duo, Model No: LP1RG - Ellex Medical PTY, LTD 82 Gilbert Street, Adelaide, S.A. 5000, AUSTRALIA. (The Integre Duo is a dual-wavelength surgical photocagulator laser intended for use in a clinic, outpatient clinic, or a retinal specialist's office. )
Product code: HQF Laser, Ophthalmic
Reason for recall: Electric Shock from Power Supply: The power supply has a defect which can cause an electrical shock to user.
Root cause tag: design
FDA root cause: Device Design
Action: Ellex, Inc. called each customer on 6/13/07, about the problem (defect which can cause electric shock) and advised that they would be performing modification of the power supply in the laser system and scheduling a field service visit to complete the work. Upon completion of the modification, the service technician completed the service record and left a copy with each client and informed them of the completed work. A copy of each completed service record was sent to Ellex Medical Pty. Ltd. On 9/27/07, Ellex sent a letter to all consignees, informing them that all modifications by service technicians' have been completed, and that their Solitaire LP4532 laser and/or Intregre Duo LP1RG is up to the manufacturers specifications and is in good operating order.
Quantity in commerce: 1
Distribution: Worldwide Distribution - USA including states of WI, PA, CO, CA, NC, NY, SC, MD, and MS, and countries of Canada and Brazil.
Product codes and lots: Integre Duo LP1RG-S P/N 3040000 (serial # /system #): 31418 / ID1057

Product code HQF

K052777Class IILaserex Duo Family of Dual Wavelength Ophthalmic Lasers Including Models Integre Duo Lp1rg-S, Lp1rg-DEllex Medical Pty, Ltd. / cleared 2006-03-16

Process control is the most common named cause of a device recall11 SEP 2026 / by Medical Device Manufacturing

About this record

Sourced from the FDA device recall database and the FDA enforcement reports, both ingested from openFDA. The recall record supplies the product, the reason and the product code; the enforcement report supplies the classification. The two datasets are exported by FDA on different days, and the date above is the older of the two, so nothing on this page is newer than it says.

MDM adds the root cause tag, derived from FDA’s own root cause text, and the cross-links to the product code, the clearances named on the record and MDM coverage. Where a recall has not been joined to an enforcement report, no classification is shown.

Data as of 2026-09-30, the FDA export date for this dataset. Page last changed 2026-09-05. View this recall on fda.gov (opens on fda.gov)