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Medline Industries, Inc. P155508DRecalls & reported problems

Medline Industries, Inc. · ER CENTRAL LINE KIT · Class 2

Data updated Oct 18, 2026 from official FDA records · Editorial policy

2 open recalls name this device. See the recall details and contact the manufacturer or your healthcare provider.

Adverse event reports
0
Deaths reported
0
Injuries reported
0
Recalls naming it
2

Summary

No MAUDE adverse event reports in our data reference this device identifier directly.

2 FDA recall records name this device's identifier, 2 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, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.

Recalls naming this device

  1. 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 · Recall details · FDA record ↗

  2. 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 ↗

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Sources and updates

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