• Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

MAUDE Adverse Event Report: Applied Medical Resources Inzii Retrieval System; Laparoscope, General & Plastic Surgery

  • Print
  • Share
  • E-mail
-
Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 

Applied Medical Resources Inzii Retrieval System; Laparoscope, General & Plastic Surgery Back to Search Results
Model Number CD001
Medical Device Problem Code Detachment of Device or Device Component (2907)
Health Effect - Clinical Code No Clinical Signs, Symptoms or Conditions (4582)
Date of Event 08/28/2026
Type of Reportable Event Malfunction
Search Alerts/Recalls

  New Search  |  Submit an Adverse Event Report

Brand Name
Inzii Retrieval System
Common Device Name
Laparoscope, General & Plastic Surgery
Manufacturer (Section D)
Applied Medical Resources
22872 avenida empresa
rancho santa margarita CA 92688
Manufacturer Contact
ashleigh mendez
22872 avenida empresa
rancho santa margarita, CA 92688
+1(949)713-5359
MDR Report Key50892481
Report Number2027111-2026-00730
Device Sequence Number17642743
Product Code GCJ
UDI-Device Identifier00607915117382
UDI-Public(01)00607915117382
Combination Product (Y/N)N
Initial Reporter CountryBE
PMA/510(K) Number
K060051
Number of Events Summarized1
Summary Report (Y/N)N
Serviced by Third Party (Y/N)N
Reporter Type Manufacturer
Report Source Foreign,Health Professional,User Facility,Company Representative
Initial Reporter Occupation Pharmacist
Type of Report Initial
Report Date (Section B) 09/24/2026
1 Device was Involved in the Event
1 Patient was Involved in the Event
Is this an Adverse Event Report? No
Is this a Product Problem Report? Yes
Operator of Device Health Professional
Device Model NumberCD001
Device Catalogue Number101473283
Device Lot Number1594316
Was Device Available for Evaluation? No
Is the Reporter a Health Professional? Yes
Was the Report Sent to FDA? No
Type of Report(Section G)Thirty-Day
Initial Date Received by Manufacturer 09/01/2026
Initial Report FDA Received Date09/24/2026
Date Device Manufactured07/03/2026
Is the Device Labeled for Single Use? (Y/N) Yes
Is This a Single-Use Device that was
Reprocessed and Reused on a Patient? (Y/N)
No
Usage of Device Initial
Patient Sequence Number1
Patient SexUnknown
-
-