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

MAUDE Adverse Event Report: ICU MEDICAL DE MEXICO, S. De R.L. De C.V. ChemoLock® w/Red Cap; Closed Antineoplastic And Hazardous Drug Reconstitution And Transfer System

  • 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
 

ICU MEDICAL DE MEXICO, S. De R.L. De C.V. ChemoLock® w/Red Cap; Closed Antineoplastic And Hazardous Drug Reconstitution And Transfer System Back to Search Results
Catalog Number CL2000S-RC
Medical Device Problem Code Fluid/Blood Leak (1250)
Health Effect - Clinical Code No Clinical Signs, Symptoms or Conditions (4582)
Date of Event 08/19/2026
Type of Reportable Event Malfunction
Search Alerts/Recalls

  New Search  |  Submit an Adverse Event Report

Brand Name
ChemoLock® w/Red Cap
Common Device Name
Closed Antineoplastic And Hazardous Drug Reconstitution And Transfer System
Manufacturer (Section D)
ICU MEDICAL DE MEXICO, S. De R.L. De C.V.
avenida cuarzo no. 250
ensenada, b.cfa. NA 22790
MX  22790
Manufacturer Contact
reed covert
951 calle amanecer
san clemente, CA 92673
+1(224)706-2300
MDR Report Key50694632
Report Number9617594-2026-01219
Device Sequence Number5975220
Product Code ONB
UDI-Device Identifier00887709091887
Combination Product (Y/N)N
Initial Reporter StateNJ
Initial Reporter CountryUS
PMA/510(K) Number
K131549
Number of Events Summarized1
Summary Report (Y/N)N
Serviced by Third Party (Y/N)N
Reporter Type Manufacturer
Report Source Health Professional,User Facility
Initial Reporter Occupation Pharmacist
Type of Report Initial
Report Date (Section B) 09/09/2026
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 Catalogue NumberCL2000S-RC
Device Lot Number14904966
Was Device Available for Evaluation? Yes
Is the Reporter a Health Professional? Yes
Type of Report(Section G)Thirty-Day
Initial Date Received by Manufacturer 08/20/2026
Initial Report FDA Received Date09/09/2026
Was Device Evaluated by Manufacturer? (Y/N) No
Date Device Manufactured03/18/2026
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 Age79 YR
Patient SexMale
Patient Weight147 LB
-
-