Centurion Medical Products CorpRecalls & reported problems across all models
Medline Industries, Inc. · 52 models in the FDA device registry
Data updated Oct 18, 2026 from official FDA records · Editorial policy
32 open recalls name at least one Centurion Medical Products Corp model. Check whether yours is affected in the recall details, and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 10
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls
- 32
We found 52 models of Centurion Medical Products Corp by Medline Industries, Inc. in the FDA's device registry (GUDID). Together they are named in 10 adverse event reports in the FDA's MAUDE database, received between Mar 19, 2026 and Sep 25, 2026 — classified as 10 malfunctions.
The most frequently reported specific device problem is “Dull, Blunt” (4 reports).
32 FDA recall records name at least one of these models by its device identifier, 32 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
Centurion Medical Products Corp 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.
- May 4, 2026Class IIOpen, Classified
During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surface finish, instances where the catheter connector detached prematurely from the catheter funnel, and limited cases where the catheter outer diameter did not meet specification.
Z-2491-2026 · Root cause: Nonconforming Material/Component · Recall details · FDA record ↗
- Apr 27, 2026Class IIOpen, Classified
Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.
Z-2424-2026 · Root cause: Process control · names 2 of these models · Recall details · FDA record ↗
- Mar 19, 2026Class IIOpen, Classified
During an internal review, Medline identified higher-than-expected endotoxin levels on a representative Medline neuro sponge product, indicating that in-market product may be out-of-specification for endotoxin.
Z-2021-2026 · Root cause: Under Investigation by firm · Recall details · FDA record ↗
- Jan 7, 2026Class IIOpen, Classified
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packaging cycles; however, the identified calibration issues have the potential to impact the sterility assurance level (SAL) of the Recalled Products.
Z-2108-2026 · Root cause: Process control · names 2 of these models · Recall details · FDA record ↗
- Jan 7, 2026Class IIOpen, Classified
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packaging cycles; however, the identified calibration issues have the potential to impact the sterility assurance level (SAL) of the Recalled Products.
Z-2101-2026 · Root cause: Process control · names 3 of these models · Recall details · FDA record ↗
- Jan 7, 2026Class IIOpen, Classified
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packaging cycles; however, the identified calibration issues have the potential to impact the sterility assurance level (SAL) of the Recalled Products.
Z-1414-2026 · Root cause: Under Investigation by firm · names 2 of these models · Recall details · FDA record ↗
- Jan 7, 2026Class IIOpen, Classified
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packaging cycles; however, the identified calibration issues have the potential to impact the sterility assurance level (SAL) of the Recalled Products.
Z-1399-2026 · Root cause: Under Investigation by firm · names 3 of these models · Recall details · FDA record ↗
- Dec 24, 2025Class IIOpen, Classified
Medline Industries, LP is issuing a recall for specific items and lots of Medline Kits containing BD ChloraPrep Triple Swabsticks which BD determined may exhibit an open seal on the packaging of the applicators.
Z-1334-2026 · Root cause: Packaging change control · names 2 of these models · Recall details · FDA record ↗
- Dec 24, 2025Class IIOpen, Classified
Medline Industries, LP is issuing a recall for specific items and lots of Medline Kits containing BD ChloraPrep Triple Swabsticks which BD determined may exhibit an open seal on the packaging of the applicators.
Z-1330-2026 · Root cause: Packaging change control · names 2 of these models · Recall details · FDA record ↗
- Dec 12, 2025Class IIOpen, Classified
Medline kits were manufactured and distributed containing MASTISOL liquid adhesive which was recalled due to complaints that the butyrate tubing cracked during actuation of the vials of MASTISOL Liquid Adhesive.
Z-1195-2026 · Root cause: Nonconforming Material/Component · Recall details · FDA record ↗
- May 15, 2025Class IIOpen, Classified
There is a possible packaging defect impacting the outer Tyvec pouch that protects the sterile product.
Z-1995-2025 · Root cause: Under Investigation by firm · Recall details · FDA record ↗
- Mar 3, 2025Class IIOpen, Classified
There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.
Z-1614-2025 · Root cause: Under Investigation by firm · Recall details · FDA record ↗
- Mar 3, 2025Class IIOpen, Classified
There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.
Z-1611-2025 · Root cause: Under Investigation by firm · Recall details · FDA record ↗
- Mar 3, 2025Class IIOpen, Classified
There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.
Z-1605-2025 · Root cause: Under Investigation by firm · Recall details · FDA record ↗
- Mar 3, 2025Class IIOpen, Classified
There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.
Z-1586-2025 · Root cause: Under Investigation by firm · Recall details · FDA record ↗
- Sep 4, 2024Class IIOpen, Classified
XXX
Z-0166-2025 · Root cause: Under Investigation by firm · names 3 of these models · Recall details · FDA record ↗
- Sep 4, 2024Class IIOpen, Classified
It has been determined that certain Convenience kits that were packaged in breather pouch lot 323080002 may result in the potential of using non-sterile product if the vendor seal of the pouch is opened/unsealed.
Z-0162-2025 · Root cause: Under Investigation by firm · Recall details · FDA record ↗
- Sep 4, 2024Class IIOpen, Classified
It has been determined that certain Convenience kits that were packaged in breather pouch lot 323080002 may result in the potential of using non-sterile product if the vendor seal of the pouch is opened/unsealed.
Z-0151-2025 · Root cause: Under Investigation by firm · Recall details · FDA record ↗
- Nov 15, 2023Class IOpen, Classified
Medline Industries, LP is recalling certain kits and trays that were manufactured using specific lots of Nurse Assist (as components): 0.9% Sodium Chloride Irrigation USP, Sterile Water for Irrigation USP and Saline Flush Syringe. Nurse Assist issued a recall due to the potential lack of sterility, which could result in the solution being non sterile.
Z-1117-2024 · Root cause: Nonconforming Material/Component · names 3 of these models · Recall details · FDA record ↗
- Nov 15, 2023Class IOpen, Classified
Medline Industries, LP is recalling certain kits and trays that were manufactured using specific lots of Nurse Assist (as components): 0.9% Sodium Chloride Irrigation USP, Sterile Water for Irrigation USP and Saline Flush Syringe. Nurse Assist issued a recall due to the potential lack of sterility, which could result in the solution being non sterile.
Z-1111-2024 · Root cause: Nonconforming Material/Component · names 5 of these models · Recall details · FDA record ↗
- Nov 15, 2023Class IOpen, Classified
Medline Industries, LP is recalling certain kits and trays that were manufactured using specific lots of Nurse Assist (as components): 0.9% Sodium Chloride Irrigation USP, Sterile Water for Irrigation USP and Saline Flush Syringe. Nurse Assist issued a recall due to the potential lack of sterility, which could result in the solution being non sterile.
Z-1097-2024 · Root cause: Nonconforming Material/Component · names 7 of these models · Recall details · FDA record ↗
- Nov 15, 2023Class IOpen, Classified
Medline Industries, LP is recalling certain kits and trays that were manufactured using specific lots of Nurse Assist (as components): 0.9% Sodium Chloride Irrigation USP, Sterile Water for Irrigation USP and Saline Flush Syringe. Nurse Assist issued a recall due to the potential lack of sterility, which could result in the solution being non sterile.
Z-1096-2024 · Root cause: Nonconforming Material/Component · Recall details · FDA record ↗
- May 18, 2023Class IIOpen, Classified
Probe covers for use during diagnostic ultrasound procedures may have an inadequate barrier at the seams.
Z-2185-2023 · Root cause: Device Design · Recall details · FDA record ↗
- May 18, 2023Class IIOpen, Classified
Probe covers for use during diagnostic ultrasound procedures may have an inadequate barrier at the seams.
Z-2181-2023 · Root cause: Device Design · Recall details · FDA record ↗
- May 18, 2023Class IIOpen, Classified
Probe covers for use during diagnostic ultrasound procedures may have an inadequate barrier at the seams.
Z-2175-2023 · Root cause: Device Design · names 2 of these models · Recall details · FDA record ↗
- May 18, 2023Class IIOpen, Classified
Probe covers for use during diagnostic ultrasound procedures may have an inadequate barrier at the seams.
Z-2168-2023 · Root cause: Device Design · Recall details · FDA record ↗
- May 18, 2023Class IIOpen, Classified
Probe covers for use during diagnostic ultrasound procedures may have an inadequate barrier at the seams.
Z-2167-2023 · Root cause: Device Design · Recall details · FDA record ↗
- May 15, 2023Class IIOpen, Classified
Potential for the labeled sterile ultrasound gel component within packs to not meet sterility specifications.
Z-2325-2023 · Root cause: Nonconforming Material/Component · Recall details · FDA record ↗
- May 15, 2023Class IIOpen, Classified
Potential for the labeled sterile ultrasound gel component within packs to not meet sterility specifications.
Z-2322-2023 · Root cause: Nonconforming Material/Component · Recall details · FDA record ↗
- Dec 7, 2022Class IIOpen, Classified
The recall is due to the perforated bag not allowing for outside of the kit wrapping to be sterile, therefore, only the contents inside the kits wrapping are sterile.
Z-1128-2023 · Root cause: Under Investigation by firm · Recall details · FDA record ↗
…and 2 older recalls, listed on each model's page.
Most reported Centurion Medical Products Corp problems
Device problems
- Dull, Blunt4
- Corroded2
- Appropriate Device Problem Term/Code Not Available1
- Break1
- Failure to Align1
- Fluid/Blood Leak1
- Particulates1
Patient problems
- No Clinical Signs, Symptoms or Conditions10
Centurion Medical Products Corp models
52 models, most reported first. Each model has its own page with its reports, recalls and device details.
- Centurion Medical Products Corp MNS13935AGeneral surgery tray3 recalls0 reports
- Centurion Medical Products Corp MNS7460ALabor and Delivery Kit3 recalls0 reports
- Centurion Medical Products Corp DT22065Dressing change tray2 recalls0 reports
- Centurion Medical Products Corp DT22260Central venous catheter tray2 recalls0 reports
- Centurion Medical Products Corp MNS13555Central venous catheter tray2 recalls0 reports
- Centurion Medical Products Corp MNS13550ALabor and Delivery Kit2 recalls0 reports
- Centurion Medical Products Corp CVI680CCatheter care tray2 recalls0 reports
- Centurion Medical Products Corp MNS13935General surgery tray2 recalls0 reports
- Centurion Medical Products Corp UVT1250General surgery tray2 recalls0 reports
- Centurion Medical Products Corp MNS13935BGeneral surgery tray2 recalls0 reports
- Centurion Medical Products Corp DT16615Cardiac catheterization kit1 recall0 reports
- Centurion Medical Products Corp IVS3485AGeneral surgery tray1 recall0 reports
- Centurion Medical Products Corp MNS10395Circuit, breathing (w connector, adaptor, y piece)1 recall0 reports
- Centurion Medical Products Corp DT21230AGeneral surgery tray1 recall0 reports
- Centurion Medical Products Corp DT20355BGeneral surgery tray1 recall0 reports
- Centurion Medical Products Corp DT20350BGeneral surgery tray1 recall0 reports
- Centurion Medical Products Corp DT20345ACentral venous catheter tray1 recall0 reports
- Centurion Medical Products Corp DT21460BDressing change tray1 recall0 reports
- Centurion Medical Products Corp CVI4395BCentral venous catheter tray1 recall0 reports
- Centurion Medical Products Corp DM715ACardiovascular procedure kit1 recall0 reports
- Centurion Medical Products Corp DT20640BDressing change tray1 recall0 reports
- Centurion Medical Products Corp MNS13545General surgery tray1 recall0 reports
- Centurion Medical Products Corp UVT1165General surgery tray1 recall0 reports
- Centurion Medical Products Corp DT22785Central venous catheter tray1 recall0 reports
- Centurion Medical Products Corp DT22780Central venous catheter tray1 recall0 reports
- Centurion Medical Products Corp DT19330BCentral venous catheter tray1 recall0 reports
- Centurion Medical Products Corp MNS13650General surgery tray1 recall0 reports
- Centurion Medical Products Corp DT19740ACentral venous catheter tray1 recall0 reports
- Centurion Medical Products Corp MNS13675Ear, nose, and throat surgical tray1 recall0 reports
- Centurion Medical Products Corp IVS3635BCatheter care tray1 recall0 reports
- Centurion Medical Products Corp PT235AOrthopedic tray1 recall0 reports
- Centurion Medical Products Corp DT22705AGeneral surgery tray1 recall0 reports
- Centurion Medical Products Corp DT22810Dressing change tray1 recall0 reports
- Centurion Medical Products Corp DM1165BCardiovascular procedure kit1 recall0 reports
- Centurion Medical Products Corp MNS13635ACesarean section tray1 recall0 reports
- Centurion Medical Products Corp DT22880Dressing change tray1 recall0 reports
- Centurion Medical Products Corp MNS13965AObstetrical kit1 recall0 reports
- Centurion Medical Products Corp MNS15265General surgery tray1 recall0 reports
- Centurion Medical Products Corp SUT15830AINSTRUMENT, MANUAL, SURGICAL, GENERAL USE1 recall0 reports
- Centurion Medical Products Corp DT22790CCardiovascular procedure kit1 recall0 reports
- Centurion Medical Products Corp DM320CDressing change tray1 recall0 reports
- Centurion Medical Products Corp MNS15597Ear, nose, and throat surgical tray1 recall0 reports
- Centurion Medical Products Corp DM1120AGeneral surgery tray1 recall0 reports
- Centurion Medical Products Corp CVI3940AGeneral surgery tray1 recall0 reports
- Centurion Medical Products Corp CIT7300Circumcision tray3 reports
- Centurion Medical Products Corp 66240SCISSORS, MEDICAL, DISPOSABLE1 report
- Centurion Medical Products Corp 66450SCISSORS, GENERAL, SURGICAL1 report
- Centurion Medical Products Corp LC205Central venous catheter tray1 report
- Centurion Medical Products Corp MNS14040Ear, nose, and throat surgical tray1 report
- Centurion Medical Products Corp SUT20655BPlastic surgery and accessories kit1 report
- Centurion Medical Products Corp CIT7130ACircumcision tray1 report
- Centurion Medical Products Corp MNS15613Cardiovascular procedure kit1 report
Recent Centurion Medical Products Corp adverse event reports
The 10 most recent reports across all models, in the reporter's own words as published by the FDA.
MalfunctionSep 25, 2026Fluid/Blood Leak
It was reported that needless connector leaked when used.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50900047 ↗MalfunctionSep 17, 2026Corroded
It was reported that "MULTIPLE CENTURION INSTRUMENTS WITH RUST ON THEM/IN THE PACKAGE."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50807753 ↗MalfunctionAug 28, 2026Dull, Blunt; Failure to Align
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50509804 ↗MalfunctionJul 28, 2026Corroded
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50059400 ↗MalfunctionJul 27, 2026Dull, Blunt
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50046397 ↗MalfunctionJul 27, 2026Dull, Blunt
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50046395 ↗MalfunctionJul 27, 2026Dull, Blunt
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50046394 ↗MalfunctionJul 27, 2026Particulates
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50007987 ↗MalfunctionJun 11, 2026Break
THERE WAS A PATIENT SAFETY CONCERN IDENTIFIED DUE TO A DISPOSABLE CIRCUMCISION KIT INSTRUMENT BREAKING DURING A PROCEDURE. THERE WAS NO HARM TO THE PATIENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25470975 ↗MalfunctionMar 19, 2026Appropriate Device Problem Term/Code Not Available
ACCORDING TO THE FACILITY, THE CUTTERS WOULD NOT CUT THROUGH A THIN WIRE BRONCHOSCOPY BRUSH WIRE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24641928 ↗
Other Medline Industries, Inc. products
- NAMIC667 models · 229 reports · 22 recalls
- CURAD85 models · 295 reports · 4 recalls
- HUDSON RCI30 models · 190 reports · 2 recalls
- Excelsior8 models · 47 reports · 3 recalls
- BAUSCH and LOMB6 models · 1 reports · 2 recalls
- Medline ReNewal18 models · 34 reports · 1 recall
- Guardian15 models · 77 reports
- MEDLINE UNITE10 models · 9 reports · 1 recall
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.
How reports and recalls are matched · Editorial policy · Report an error on this page