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MEDLINERecalls & reported problems across all models

Centurion Medical Products Corporation · 9 models in the FDA device registry

Data updated Oct 16, 2026 from official FDA records · Editorial policy

8 open recalls name at least one MEDLINE model. Check whether yours is affected in the recall details, and contact the manufacturer or your healthcare provider.

Adverse event reports
0
Deaths reported
0
Injuries reported
0
Recalls
8

We found 9 models of MEDLINE by Centurion Medical Products Corporation in the FDA's device registry (GUDID). None of them is named in an adverse event report in our data.

8 FDA recall records name at least one of these models by its device identifier, 8 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 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 · Recall details · FDA record ↗

  2. Feb 23, 2024Open, Classified

    Product may have a weak seal which may result in a breach of sterility of the contents if the seal fails. The weak seal may not be detectable by all users.

    Z-1455-2024 · Root cause: Process control · Recall details · FDA record ↗

  3. Feb 23, 2024Open, Classified

    Product may have a weak seal which may result in a breach of sterility of the contents if the seal fails. The weak seal may not be detectable by all users.

    Z-1453-2024 · Root cause: Process control · Recall details · FDA record ↗

  4. May 18, 2023Open, Classified

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

    Z-2180-2023 · Root cause: Device Design · Recall details · FDA record ↗

  5. 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 · Recall details · FDA record ↗

  6. 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 2 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-2297-2023 · Root cause: Nonconforming Material/Component · Recall details · FDA record ↗

  8. Dec 7, 2022Open, 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 ↗

MEDLINE models

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

Other Centurion Medical Products Corporation products

All Centurion Medical Products Corporation devices →

Sources and updates

How reports and recalls are matched · Editorial policy · Report an error on this page