V. MuellerRecalls & reported problems across all models
Carefusion 2200, Inc · 47 models in the FDA device registry
Data updated Oct 18, 2026 from official FDA records · Editorial policy
18 open recalls name at least one V. Mueller model. Check whether yours is affected in the recall details, and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls
- 18
We found 47 models of V. Mueller by Carefusion 2200, Inc in the FDA's device registry (GUDID). Together they are named in 2 adverse event reports in the FDA's MAUDE database, received between Jul 17, 2023 and Nov 2, 2023 — classified as 1 injury, 1 malfunction.
The most frequently reported specific device problem is “Detachment of Device or Device Component” (1 report).
18 FDA recall records name at least one of these models by its device identifier, 18 still open.
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event. Widely used products collect more reports, so totals can't be used to compare products or estimate failure rates. Only reports that name a model's exact device identifier are counted. What reports can and can't tell you · How this data works
Reports received per month, all models
V. Mueller recalls
FDA recall records that name at least one of these models by its device identifier, newest first. Each recall usually covers specific models or lots, so check the details.
- Jan 30, 2023Class IIOpen, Classified
Product did not meet shelf-life testing requirements resulting in a breach of the sterility of the Genesis container holding surgical equipment.
Z-1236-2023 · Root cause: Packaging change control · names 28 of these models · Recall details · FDA record ↗
- Sep 26, 2022Class IIOpen, Classified
Genesis STERRAD Reusable Rigid Sterilization Containers have not consistently met the requirements for aerosol challenge testing.
Z-0219-2023 · Root cause: Under Investigation by firm · Recall details · FDA record ↗
- Sep 26, 2022Class IIOpen, Classified
Genesis STERRAD Reusable Rigid Sterilization Containers have not consistently met the requirements for aerosol challenge testing.
Z-0218-2023 · Root cause: Under Investigation by firm · Recall details · FDA record ↗
- Sep 26, 2022Class IIOpen, Classified
Genesis STERRAD Reusable Rigid Sterilization Containers have not consistently met the requirements for aerosol challenge testing.
Z-0217-2023 · Root cause: Under Investigation by firm · Recall details · FDA record ↗
- Sep 26, 2022Class IIOpen, Classified
Genesis STERRAD Reusable Rigid Sterilization Containers have not consistently met the requirements for aerosol challenge testing.
Z-0216-2023 · Root cause: Under Investigation by firm · Recall details · FDA record ↗
- Sep 26, 2022Class IIOpen, Classified
Genesis STERRAD Reusable Rigid Sterilization Containers have not consistently met the requirements for aerosol challenge testing.
Z-0215-2023 · Root cause: Under Investigation by firm · Recall details · FDA record ↗
- Sep 26, 2022Class IIOpen, Classified
Genesis STERRAD Reusable Rigid Sterilization Containers have not consistently met the requirements for aerosol challenge testing.
Z-0214-2023 · Root cause: Under Investigation by firm · Recall details · FDA record ↗
- Sep 26, 2022Class IIOpen, Classified
Genesis STERRAD Reusable Rigid Sterilization Containers have not consistently met the requirements for aerosol challenge testing.
Z-0213-2023 · Root cause: Under Investigation by firm · Recall details · FDA record ↗
- Sep 26, 2022Class IIOpen, Classified
Genesis STERRAD Reusable Rigid Sterilization Containers have not consistently met the requirements for aerosol challenge testing.
Z-0212-2023 · Root cause: Under Investigation by firm · Recall details · FDA record ↗
- Sep 26, 2022Class IIOpen, Classified
Genesis STERRAD Reusable Rigid Sterilization Containers have not consistently met the requirements for aerosol challenge testing.
Z-0211-2023 · Root cause: Under Investigation by firm · Recall details · FDA record ↗
- Sep 26, 2022Class IIOpen, Classified
Genesis STERRAD Reusable Rigid Sterilization Containers have not consistently met the requirements for aerosol challenge testing.
Z-0210-2023 · Root cause: Under Investigation by firm · Recall details · FDA record ↗
- Sep 26, 2022Class IIOpen, Classified
Genesis STERRAD Reusable Rigid Sterilization Containers have not consistently met the requirements for aerosol challenge testing.
Z-0209-2023 · Root cause: Under Investigation by firm · Recall details · FDA record ↗
- Sep 26, 2022Class IIOpen, Classified
Genesis STERRAD Reusable Rigid Sterilization Containers have not consistently met the requirements for aerosol challenge testing.
Z-0208-2023 · Root cause: Under Investigation by firm · Recall details · FDA record ↗
- Sep 26, 2022Class IIOpen, Classified
Genesis STERRAD Reusable Rigid Sterilization Containers have not consistently met the requirements for aerosol challenge testing.
Z-0207-2023 · Root cause: Under Investigation by firm · Recall details · FDA record ↗
- Sep 26, 2022Class IIOpen, Classified
Genesis STERRAD Reusable Rigid Sterilization Containers have not consistently met the requirements for aerosol challenge testing.
Z-0206-2023 · Root cause: Under Investigation by firm · Recall details · FDA record ↗
- Sep 26, 2022Class IIOpen, Classified
Genesis STERRAD Reusable Rigid Sterilization Containers have not consistently met the requirements for aerosol challenge testing.
Z-0205-2023 · Root cause: Under Investigation by firm · Recall details · FDA record ↗
- Sep 26, 2022Class IIOpen, Classified
Genesis STERRAD Reusable Rigid Sterilization Containers have not consistently met the requirements for aerosol challenge testing.
Z-0204-2023 · Root cause: Under Investigation by firm · Recall details · FDA record ↗
- Sep 26, 2022Class IIOpen, Classified
Genesis STERRAD Reusable Rigid Sterilization Containers have not consistently met the requirements for aerosol challenge testing.
Z-0203-2023 · Root cause: Under Investigation by firm · Recall details · FDA record ↗
Most reported V. Mueller problems
Device problems
- Detachment of Device or Device Component1
- Mechanical Problem1
Patient problems
- Laceration(s)1
- No Clinical Signs, Symptoms or Conditions1
V. Mueller models
47 models, most reported first. Each model has its own page with its reports, recalls and device details.
- V. Mueller CD0-3STSterilization wrap containers, trays, cassettes & other accessories1 recall0 reports
- V. Mueller CD0-4STSterilization wrap containers, trays, cassettes & other accessories1 recall0 reports
- V. Mueller CD1-4STSterilization wrap containers, trays, cassettes & other accessories1 recall0 reports
- V. Mueller CD1-5STSterilization wrap containers, trays, cassettes & other accessories1 recall0 reports
- V. Mueller CD1-6STSterilization wrap containers, trays, cassettes & other accessories1 recall0 reports
- V. Mueller CD2-4STSterilization wrap containers, trays, cassettes & other accessories1 recall0 reports
- V. Mueller CD2-5STSterilization wrap containers, trays, cassettes & other accessories1 recall0 reports
- V. Mueller CD2-6STSterilization wrap containers, trays, cassettes & other accessories1 recall0 reports
- V. Mueller CD2-8STSterilization wrap containers, trays, cassettes & other accessories1 recall0 reports
- V. Mueller CD3-4STSterilization wrap containers, trays, cassettes & other accessories1 recall0 reports
- V. Mueller CD3-5STSterilization wrap containers, trays, cassettes & other accessories1 recall0 reports
- V. Mueller CD3-6STSterilization wrap containers, trays, cassettes & other accessories1 recall0 reports
- V. Mueller CD3-7STSterilization wrap containers, trays, cassettes & other accessories1 recall0 reports
- V. Mueller CD4-3STSterilization wrap containers, trays, cassettes & other accessories1 recall0 reports
- V. Mueller CD4-5STSterilization wrap containers, trays, cassettes & other accessories1 recall0 reports
- V. Mueller CD5-3BSterilization wrap containers, trays, cassettes & other accessories1 recall0 reports
- V. Mueller CD5-3CSterilization wrap containers, trays, cassettes & other accessories1 recall0 reports
- V. Mueller CD5-3STSterilization wrap containers, trays, cassettes & other accessories1 recall0 reports
- V. Mueller CD5-61BSterilization wrap containers, trays, cassettes & other accessories1 recall0 reports
- V. Mueller CD5-61CSterilization wrap containers, trays, cassettes & other accessories1 recall0 reports
- V. Mueller CD5-61STSterilization wrap containers, trays, cassettes & other accessories1 recall0 reports
- V. Mueller CD5-3C-GOLDSterilization wrap containers, trays, cassettes & other accessories1 recall0 reports
- V. Mueller CD5-3C-PURPLESterilization wrap containers, trays, cassettes & other accessories1 recall0 reports
- V. Mueller CD5-3C-BLUESterilization wrap containers, trays, cassettes & other accessories1 recall0 reports
- V. Mueller CD5-3C-GREENSterilization wrap containers, trays, cassettes & other accessories1 recall0 reports
- V. Mueller CD5-3C-BLACKSterilization wrap containers, trays, cassettes & other accessories1 recall0 reports
- V. Mueller CD5-61C-GOLDSterilization wrap containers, trays, cassettes & other accessories1 recall0 reports
- V. Mueller CD5-61C-PURPLESterilization wrap containers, trays, cassettes & other accessories1 recall0 reports
- V. Mueller CD5-61C-BLUESterilization wrap containers, trays, cassettes & other accessories1 recall0 reports
- V. Mueller CD5-61C-GREENSterilization wrap containers, trays, cassettes & other accessories1 recall0 reports
- V. Mueller CD5-61C-REDSterilization wrap containers, trays, cassettes & other accessories1 recall0 reports
- V. Mueller CD5-61C-BLACKSterilization wrap containers, trays, cassettes & other accessories1 recall0 reports
- V. Mueller CD5-3B-GOLDSterilization wrap containers, trays, cassettes & other accessories1 recall0 reports
- V. Mueller CD5-3B-PURPLESterilization wrap containers, trays, cassettes & other accessories1 recall0 reports
- V. Mueller CD5-3B-BLUESterilization wrap containers, trays, cassettes & other accessories1 recall0 reports
- V. Mueller CD5-3B-GREENSterilization wrap containers, trays, cassettes & other accessories1 recall0 reports
- V. Mueller CD5-3B-REDSterilization wrap containers, trays, cassettes & other accessories1 recall0 reports
- V. Mueller CD5-3B-BLACKSterilization wrap containers, trays, cassettes & other accessories1 recall0 reports
- V. Mueller CD5-61B-GOLDSterilization wrap containers, trays, cassettes & other accessories1 recall0 reports
- V. Mueller CD5-61B-PURPLESterilization wrap containers, trays, cassettes & other accessories1 recall0 reports
- V. Mueller CD5-61B-BLUESterilization wrap containers, trays, cassettes & other accessories1 recall0 reports
- V. Mueller CD5-61B-GREENSterilization wrap containers, trays, cassettes & other accessories1 recall0 reports
- V. Mueller CD5-61B-REDSterilization wrap containers, trays, cassettes & other accessories1 recall0 reports
- V. Mueller CD5-61B-BLACKSterilization wrap containers, trays, cassettes & other accessories1 recall0 reports
- V. Mueller CD5-3C-REDSterilization wrap containers, trays, cassettes & other accessories1 recall0 reports
- V. Mueller GL7021CLAMP, CIRCUMCISION1 report
- V. Mueller F265.00Electrosurgical, cutting & coagulation & accessories1 report
Recent V. Mueller adverse event reports
The 2 most recent reports across all models, in the reporter's own words as published by the FDA.
MalfunctionNov 2, 2023Detachment of Device or Device Component; Detachment of Device or Device Component
THE USER FACILITY REPORTED VIA MEDWATCH (B)(4) THAT DURING A PATIENT PROCEDURE, THE SURGEON REMOVED THE L-HOOK AND THE NURSE OBSERVED THE CAUTERY TIP WAS NO LONGER IN PLACE. AN ABDOMINAL X-RAY WAS TAKEN OF THE PATIENT FOLLOWING THE PROCEDURE AND NO ISSUES WERE NOTED. NO INJURIES WERE REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18062260 ↗InjuryJul 17, 2023Mechanical Problem; Mechanical Problem
IT WAS REPORTED BY THE CUSTOMER THAT WHEN CLAMP WAS REMOVED, THE BABY WAS NOTED TO BE BLEEDING AND A PORTION OF THE RIGHT GLANS WAS CUT OFF IN THE CUT FORESKIN. COMPLAINT RECEIVED VIA EMAIL. CONSENT OBTAINED BY RN. RN DID CONFIRM THAT MD HAD GONE OVER THE RISKS AND BENEFITS BEFORE SHE OBTAINED THE PARENT'S SIGNATURE AND WITNESSED THE CONSENT. MD USED A MOGAN CLAMP TO PERFORM THE PROCEDURE. A TIME OUT WAS PERFORMED PRIOR TO THE PROCEDURE. MD PROCEEDED WITH THE PROCEDURE AND USED THE CLAMP. PROBE WAS USED TO LYSE ADHESIONS BETWEEN FORESKIN AND GLANS. MOGEN CLAMP WAS PLACED BEVEL DOWN. FORESKIN WAS CUT WITH SCALPEL. WHEN CLAMP WAS REMOVED, THE BABY WAS NOTED TO BE BLEEDING AND A PORTION OF THE RIGHT GLANS WAS CUT OFF IN THE CUT FORESKIN. THE PIECE OF THE GLANS WAS RETRIEVED AND PLACED IMMEDIATELY ON ICE WHILE PRESSURE WAS APPLIED BY ANOTHER MD THE ENTIRE TIME. CONTINUOUS PRESSURE APPLIED TO GLANS FOR HEMOSTASIS. THE NEONATOLOGIST WAS CALLED RIGHT AWAY AND THE BABY WAS TRANSFERRED TO THE NICU. THE NICU CALLED (B)(6) RIGHT AWAY TO TRANSFER THE BABY TO (B)(6) TO HAVE UROLOGY REATTACH CUT OFF PORTION OF THE GLANS, AND THE TEAM GAVE US AN ETA OF 20 MINUTES. MD DID INFORM THE PARENTS RIGHT
Patient problems: Laceration(s)
MAUDE report 17333882 ↗
Other Carefusion 2200, Inc products
All Carefusion 2200, Inc devices →Sources and updates
- Models: FDA GUDID, file dated Oct 13, 2026. Models are grouped by the brand name the manufacturer registered.
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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