Medline Industries, Inc.Recalls & reported problems across all models

We found 185 models of Medline Industries, Inc. by Centurion Medical Products Corporation in the FDA's device registry (GUDID). Together they are named in 4 adverse event reports in the FDA's MAUDE database, received between Mar 8, 2021 and Mar 10, 2026 — classified as 4 malfunctions.

The most frequently reported specific device problem is “Component Missing” (1 report).

11 FDA recall records name at least one of these models by its device identifier, 11 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

Medline Industries, Inc. 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.

1. May 21, 2026Open, Classified

   The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). A recall notice was issued by Huons Co., Ltd. for Lidocaine Ampules due to quality issues identified during a recent FDA manufacturing inspection of its drug manufacturing site.

   Z-2541-2026 · Root cause: Nonconforming Material/Component · names 4 of these models · Recall details · FDA record ↗

2. May 21, 2026Open, Classified

   The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). A recall notice was issued by Huons Co., Ltd. for Lidocaine Ampules due to quality issues identified during a recent FDA manufacturing inspection of its drug manufacturing site.

   Z-2538-2026 · Root cause: Nonconforming Material/Component · names 2 of these models · Recall details · FDA record ↗

3. May 21, 2026Open, Classified

   The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). A recall notice was issued by Huons Co., Ltd. for Lidocaine Ampules due to quality issues identified during a recent FDA manufacturing inspection of its drug manufacturing site.

   Z-2536-2026 · Root cause: Nonconforming Material/Component · names 18 of these models · Recall details · FDA record ↗

4. Jan 7, 2026Open, 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-2092-2026 · Root cause: Process control · Recall details · FDA record ↗

5. May 18, 2023Open, Classified

   Probe covers for use during diagnostic ultrasound procedures may have an inadequate barrier at the seams.

   Z-2195-2023 · Root cause: Device Design · Recall details · FDA record ↗

6. May 18, 2023Open, Classified

   Probe covers for use during diagnostic ultrasound procedures may have an inadequate barrier at the seams.

   Z-2194-2023 · Root cause: Device Design · names 79 of these models · Recall details · FDA record ↗

7. May 15, 2023Open, Classified

   Potential for the labeled sterile ultrasound gel component within packs to not meet sterility specifications.

   Z-2319-2023 · Root cause: Nonconforming Material/Component · Recall details · FDA record ↗

8. May 15, 2023Open, Classified

   Potential for the labeled sterile ultrasound gel component within packs to not meet sterility specifications.

   Z-2304-2023 · Root cause: Nonconforming Material/Component · names 2 of these models · Recall details · FDA record ↗

9. May 15, 2023Open, Classified

   Potential for the labeled sterile ultrasound gel component within packs to not meet sterility specifications.

   Z-2299-2023 · Root cause: Nonconforming Material/Component · names 86 of these models · Recall details · FDA record ↗

10. May 15, 2023Open, Classified

    Potential for the labeled sterile ultrasound gel component within packs to not meet sterility specifications.

    Z-2298-2023 · Root cause: Nonconforming Material/Component · names 45 of these models · Recall details · FDA record ↗

11. May 15, 2023Open, Classified

    Potential for the labeled sterile ultrasound gel component within packs to not meet sterility specifications.

    Z-2297-2023 · Root cause: Nonconforming Material/Component · names 35 of these models · Recall details · FDA record ↗

Most reported Medline Industries, Inc. problems

Medline Industries, Inc. models

185 models, 100 per page, most reported first. Each model has its own page with its reports, recalls and device details.

• Medline Industries, Inc. ECVC2750

  Cardiac catheterization kit
  3 recalls0 reports
• Medline Industries, Inc. ECVC2745

  Cardiac catheterization kit
  3 recalls0 reports
• Medline Industries, Inc. ECVC2001

  Cardiac catheterization kit
  3 recalls0 reports
• Medline Industries, Inc. ECVC5540A

  Cardiac catheterization kit
  3 recalls0 reports
• Medline Industries, Inc. ECVC5200

  Cardiac catheterization kit
  3 recalls0 reports
• Medline Industries, Inc. ECVC6505

  Cardiac catheterization kit
  3 recalls0 reports
• Medline Industries, Inc. ECVC2555

  Cardiac catheterization kit
  3 recalls0 reports
• Medline Industries, Inc. ECVC6845

  Cardiac catheterization kit
  3 recalls0 reports
• Medline Industries, Inc. ECVC2320

  Cardiac catheterization kit
  2 recalls0 reports
• Medline Industries, Inc. ECVC2720

  Cardiac catheterization kit
  2 recalls0 reports
• Medline Industries, Inc. ECVC2770

  Cardiac catheterization kit
  2 recalls0 reports
• Medline Industries, Inc. ECVC2895

  Cardiac catheterization kit
  2 recalls0 reports
• Medline Industries, Inc. ECVC3460

  Cardiac catheterization kit
  2 recalls0 reports
• Medline Industries, Inc. ECVC4880

  Cardiac catheterization kit
  2 recalls0 reports
• Medline Industries, Inc. ECVC6370

  General Surgery Tray
  2 recalls0 reports
• Medline Industries, Inc. ECVC3355

  Cardiac catheterization kit
  2 recalls0 reports
• Medline Industries, Inc. ECVC3155

  Cardiac catheterization kit
  2 recalls0 reports
• Medline Industries, Inc. ECVC2560

  Cardiac catheterization kit
  2 recalls0 reports
• Medline Industries, Inc. ECVC2240A

  Cardiac catheterization kit
  2 recalls0 reports
• Medline Industries, Inc. ECVC1915

  Cardiac catheterization kit
  2 recalls0 reports
• Medline Industries, Inc. ECVC1725

  Cardiac catheterization kit
  2 recalls0 reports
• Medline Industries, Inc. ECVC1345A

  Cardiac catheterization kit
  2 recalls0 reports
• Medline Industries, Inc. ECVC3505

  Cardiac catheterization kit
  2 recalls0 reports
• Medline Industries, Inc. ECVC3545

  Cardiac catheterization kit
  2 recalls0 reports
• Medline Industries, Inc. ECVC3735A

  Cardiac catheterization kit
  2 recalls0 reports
• Medline Industries, Inc. ECVC3755A

  Cardiac catheterization kit
  2 recalls0 reports
• Medline Industries, Inc. ECVC3900

  Cardiac catheterization kit
  2 recalls0 reports
• Medline Industries, Inc. ECVC4300

  Cardiac catheterization kit
  2 recalls0 reports
• Medline Industries, Inc. ECVC5020

  Cardiac catheterization kit
  2 recalls0 reports
• Medline Industries, Inc. ECVC6800

  Cardiac catheterization kit
  2 recalls0 reports
• Medline Industries, Inc. ECVC6815

  Cardiac catheterization kit
  2 recalls0 reports
• Medline Industries, Inc. ECVC4985

  Cardiac catheterization kit
  2 recalls0 reports
• Medline Industries, Inc. ECVC6550

  Cardiac catheterization kit
  2 recalls0 reports
• Medline Industries, Inc. ECVC4995

  Cardiac catheterization kit
  2 recalls0 reports
• Medline Industries, Inc. ECVC5010A

  Cardiac catheterization kit
  2 recalls0 reports
• Medline Industries, Inc. ECVC2940

  Cardiac catheterization kit
  2 recalls0 reports
• Medline Industries, Inc. ECVC2930

  Cardiac catheterization kit
  2 recalls0 reports
• Medline Industries, Inc. ECVC1320

  Cardiac catheterization kit
  2 recalls0 reports
• Medline Industries, Inc. ECVC6070

  Cardiac catheterization kit
  2 recalls0 reports
• Medline Industries, Inc. ECVC4135

  Cardiac catheterization kit
  2 recalls0 reports
• Medline Industries, Inc. ECVC3785

  Cardiac catheterization kit
  2 recalls0 reports
• Medline Industries, Inc. ECVC3810

  Cardiac catheterization kit
  2 recalls0 reports
• Medline Industries, Inc. ECVC4615

  Cardiac catheterization kit
  2 recalls0 reports
• Medline Industries, Inc. ECVC5270

  Cardiac catheterization kit
  2 recalls0 reports
• Medline Industries, Inc. ECVC5310

  Cardiac catheterization kit
  2 recalls0 reports
• Medline Industries, Inc. ECVC6555

  Cardiac catheterization kit
  2 recalls0 reports
• Medline Industries, Inc. ECVC5815

  Cardiac catheterization kit
  2 recalls0 reports
• Medline Industries, Inc. ECVC5810

  Cardiac catheterization kit
  2 recalls0 reports
• Medline Industries, Inc. ECVC5650

  Cardiac catheterization kit
  2 recalls0 reports
• Medline Industries, Inc. ECVC6260

  Cardiac catheterization kit
  2 recalls0 reports
• Medline Industries, Inc. ECVC5560A

  Cardiac catheterization kit
  2 recalls0 reports
• Medline Industries, Inc. ECVC5385

  Cardiac catheterization kit
  2 recalls0 reports
• Medline Industries, Inc. ECVC6255

  Cardiac catheterization kit
  2 recalls0 reports
• Medline Industries, Inc. ECVC6120

  Cardiac catheterization kit
  2 recalls0 reports
• Medline Industries, Inc. ECVC6690

  Cardiac catheterization kit
  2 recalls0 reports
• Medline Industries, Inc. ECVC6825A

  Cardiac catheterization kit
  2 recalls0 reports
• Medline Industries, Inc. ECVC6970

  Cardiac catheterization kit
  2 recalls0 reports
• Medline Industries, Inc. ECVC6920

  Cardiac catheterization kit
  2 recalls0 reports
• Medline Industries, Inc. ECVC6915

  Cardiac catheterization kit
  2 recalls0 reports
• Medline Industries, Inc. ECVC6835

  Cardiac catheterization kit
  2 recalls0 reports
• Medline Industries, Inc. STCVC2000

  Catheter introducer kit
  2 recalls0 reports
• Medline Industries, Inc. ECVC6765

  Cardiac catheterization kit
  2 recalls0 reports
• Medline Industries, Inc. ECVC6680A

  Cardiac catheterization kit
  2 recalls0 reports
• Medline Industries, Inc. ECVC6595

  Cardiac catheterization kit
  2 recalls0 reports
• Medline Industries, Inc. ECVC5655

  Cardiac catheterization kit
  2 recalls0 reports
• Medline Industries, Inc. ECVC5660

  Cardiac catheterization kit
  2 recalls0 reports
• Medline Industries, Inc. ECVC5080

  Cardiac catheterization kit
  2 recalls0 reports
• Medline Industries, Inc. ECVC5475

  Cardiac catheterization kit
  2 recalls0 reports
• Medline Industries, Inc. ECVC5525A

  Cardiac catheterization kit
  2 recalls0 reports
• Medline Industries, Inc. ECVC5870A

  Cardiac catheterization kit
  2 recalls0 reports
• Medline Industries, Inc. ECVC6020A

  Cardiac catheterization kit
  2 recalls0 reports
• Medline Industries, Inc. ECVC6075

  Cardiac catheterization kit
  2 recalls0 reports
• Medline Industries, Inc. ECVC2965

  Cardiac catheterization kit
  2 recalls0 reports
• Medline Industries, Inc. ECVC3395

  Cardiac catheterization kit
  2 recalls0 reports
• Medline Industries, Inc. ECVC6850

  Cardiac catheterization kit
  2 recalls0 reports
• Medline Industries, Inc. ECVC6585A

  Cardiac catheterization kit
  2 recalls0 reports
• Medline Industries, Inc. ECVC5015

  Cardiac catheterization kit
  2 recalls0 reports
• Medline Industries, Inc. ECVC6655A

  Cardiac catheterization kit
  2 recalls0 reports
• Medline Industries, Inc. ECVC6540

  Cardiac catheterization kit
  2 recalls0 reports
• Medline Industries, Inc. ECVC5480

  Cardiac catheterization kit
  2 recalls0 reports
• Medline Industries, Inc. ECVC5315

  Cardiac catheterization kit
  2 recalls0 reports
• MEDLINE INDUSTRIES, INC. ECVC5665

  Cardiac catheterization kit
  2 recalls0 reports
• Medline Industries, Inc. ECVC6225A

  Cardiac catheterization kit
  1 recall2 reports
• Medline Industries, Inc. ECVC1525

  Cardiac catheterization kit
  1 recall1 report
• Medline Industries, Inc. ECVC3260

  Cardiac catheterization kit
  1 recall0 reports
• Medline Industries, Inc. ECVC255

  Cardiac catheterization kit
  1 recall0 reports
• Medline Industries, Inc. ECVC1555

  Cardiac catheterization kit
  1 recall0 reports
• Medline Industries, Inc. ECVC105

  Cardiac catheterization kit
  1 recall0 reports
• Medline Industries, Inc. ECVC1300

  Cardiac catheterization kit
  1 recall0 reports
• Medline Industries, Inc. ECVC400

  Cardiac catheterization kit
  1 recall0 reports
• Medline Industries, Inc. ECVC705

  Cardiac catheterization kit
  1 recall0 reports
• Medline Industries, Inc. ECVC1140A

  Cardiac catheterization kit
  1 recall0 reports
• Medline Industries, Inc. ECVC1377

  Cardiac catheterization kit
  1 recall0 reports
• Medline Industries, Inc. ECVC1490

  Cardiac catheterization kit
  1 recall0 reports
• Medline Industries, Inc. ECVC1710

  Cardiac catheterization kit
  1 recall0 reports
• Medline Industries, Inc. ECVC2205

  Cardiac catheterization kit
  1 recall0 reports
• Medline Industries, Inc. ECVC2305

  Cardiac catheterization kit
  1 recall0 reports
• Medline Industries, Inc. ECVC2335

  Cardiac catheterization kit
  1 recall0 reports
• Medline Industries, Inc. ECVC2595

  Cardiac catheterization kit
  1 recall0 reports
• Medline Industries, Inc. ECVC3440

  Cardiac catheterization kit
  1 recall0 reports

Recent Medline Industries, Inc. adverse event reports

The 4 most recent reports across all models, in the reporter's own words as published by the FDA.

• MalfunctionMar 10, 2026Insufficient Device Problem Information

  ACCORDING TO THE FACILITY "WE HAD AN ADVANCED VENOUS ACCESS DEVICE THAT WHEN THE ANESTHESIA PROVIDER PUT IT IN THE PATIENT IT LEAKED AND THEY REMOVED IT FROM THE PATIENT".

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24561271 ↗
• MalfunctionJul 30, 2025Retraction Problem; Detachment of Device or Device Component; No Flow

  EVENT 1 [DATE REDACTED] LOT: 2025030690: PLACEMENT OF CENTRAL LINE CATHETER - VANTEX CVC [CENTRAL VENOUS CATHETER] ANTIMICROBIAL 3 LUMEN, 7FR, 20CM, LOT #2025030690. SUCCESSFUL PLACEMENT OF CVC, CONFIRMED BY XR [X-RAY] TERMINATING IN THE SVC. BLOOD RETURN NOT PRESENT ON BLUE AND WHITE LUMEN, MINIMALLY PRESENT ON BROWN PORT WITH POSITIONING AND LAYING PATIENT SUPINE. EVENT 2 [DATE REDACTED] LOT: N/A: NO BLOOD RETURN FROM WHITE PORT OF TLC [TRIPLE LUMEN CATHETER] LINED PLACED [DATE REDACTED]. EVENT 3 [DATE REDACTED] LOT: 2025030690: VANTEX LEFT FEMORAL TLC INSERTED [DATE REDACTED]. NO BLOOD RETURN DOCUMENTED BY RN ON MEDIAL (BLUE) AND PROXIMAL (WHITE) PORTS. UPON ASSESSMENT THIS MORNING UNABLE TO DRAW BACK ON EITHER PORT BUT INFUSING WITH NO ISSUES. EVENT 4 [DATE REDACTED] LOT: 2025030690: VANTEX TLC INSERTION PER PROVIDER, NO BLOOD RETURN ON DISTAL BROWN PORT ON INSERTION PER PROVIDER AND NOTE. RN HAD NO BLOOD RETURN ON DISTAL BROWN PORT EITHER. PROVIDER ALSO NOTED DURING INSERTION THE NEEDLE FELL OFF THE SUTURE LINE. UNABLE TO FINISH NEEDED A SUPPLEMENTAL SUTURE KIT TO COMPLETE. EVENT 5 [DATE REDACTED] LOT: N/A: PATIENT HAD A RIGHT INTRAJUGULAR TRIPLE LUMEN CATHETER (TLC) THAT LOST

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22663921 ↗
• MalfunctionJan 24, 2023Component Missing

  NURSING WAS ASSISTING PHYSICIAN WITH LEFT IJ TRIPLE LUMEN CATHETER PLACEMENT. WHEN THE PHYSICIAN OPENED THE SUTURE PACKAGING TO SECURE THE NEWLY PLACED LINE, THE PACKET WAS EMPTY. THE SUTURE WAS UNABLE TO BE LOCATED IN THE REST OF THE KIT. NO KNOWN HARM TO PATIENT. EXTRA EQUIPMENT NEEDED TO BE OBTAINED TO COMPLETE THE PROCEDURE. MINOR DELAY. MANUFACTURER RESPONSE FOR CARDIAC CATHETERIZATION KIT, MEDLINE INDUSTRIES, INC. (PER SITE REPORTER).

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 16232732 ↗
• MalfunctionMar 8, 2021Crack; Pressure Problem

  MIDDLE-AGED FEMALE WITH HISTORY OF DIABETES, HYPERTENSION, (B)(6), ESOPHAGEAL VARICES AND ASYSTOLE ARREST X 1. NEEDLE USED TO ACCESS VESSEL FOR TRIPLE LUMEN INSERTION HAD A CRACKED HEAD. THIS PREVENTED NEGATIVE PRESSURE FROM BEING APPLIED WHEN ATTEMPTING TO ACCESS VESSEL. PATIENT STUCK MULTIPLE TIMES BEFORE THE PROBLEM WAS IDENTIFIED. NO KNOWN HARM TO PATIENT AT THIS TIME.

  Patient problems: Insufficient Information

  MAUDE report 11434943 ↗

Other Centurion Medical Products Corporation products

• MEDLINE9 models · 0 reports · 8 recalls