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Medline Industries, Inc.

MEDLINE INDUSTRIES, INC. · Model CDS840215O · UDI-DI 10193489448993

FCH Prescription
2
510(k) clearances
6
Adverse events
14
Recalls
26
Facilities

Description

FETOSCOPY CDS-LF

Recalls

DateFirmReason
2025-09-04American Contract Systems Inc.Identified products were re-gassed (sterilized more than once) after a nonconformance occurred during the initial Ethylene Oxide (EO) gas injection process. These products have not
2024-05-06American Contract Systems, Inc.Product released with insufficient aeration time impacting the kits sterilized on the same cycle or in the same aeration chamber, which may have been compromised in sterility
2024-04-08MEDLINE INDUSTRIES, LP - NorthfieldMedical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/ other quality issues have been identified that ma
2023-11-29American Contract Systems, Inc.During an internal investigation, ACS identified that several components were "piggybacked" to ACS trays and subjected to the ACS sterilization process. There is no supporting docu
2023-05-18MEDLINE INDUSTRIES, LP - NorthfieldProbe covers for use during diagnostic ultrasound procedures may have an inadequate barrier at the seams.
2023-05-15MEDLINE INDUSTRIES, LP - NorthfieldPotential for the labeled sterile ultrasound gel component within packs to not meet sterility specifications.
2022-12-27MEDLINE INDUSTRIES, LP - NorthfieldThe convenience trays had improper placement of some of the components that were in the nonsterile portion of the tray, thus, not receiving sterilization.
2022-11-17MEDLINE INDUSTRIES, LP - NorthfieldSterile blades within sterile kits have the potential for the blade to puncture the outer foil layer of the sterile packaging.
2022-02-22Busse Hospital Disposables, Inc.Busse Convenience kits contain one or more swab/swabstick drug products, manufactured by Professional Disposables International (PDI), that are subject to a drug recall due to unce
2022-02-22Busse Hospital Disposables, Inc.Busse Convenience kits contain one or more swab/swabstick drug products, manufactured by Professional Disposables International (PDI), that are subject to a drug recall due to unce

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.