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Samco Clicktainer

Thermo Fisher Scientific (Monterrey), S. de R.L. de C.V. · Model 90ORG53-1001 · UDI-DI 17503025060269

FMH Prescription
10
510(k) clearances
556
Adverse events
21
Recalls
302
Facilities

Description

90ML/53MM CLK LBL OR CAP ST DP STERILE

Recalls

DateFirmReason
2026-03-19Medline Industries, LPDuring 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-o
2026-01-07Medline Industries, LPMedline 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 packag
2026-01-07Medline Industries, LPMedline 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 packag
2025-04-04Klinika Mdical GmbPotential for microbial contamination.
2025-04-04Klinika Mdical GmbPotential for microbial contamination.
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
2024-02-23MEDLINE INDUSTRIES, LP - NorthfieldProduct 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.
2023-10-19Meridian Bioscience IncPlastic vials contain a manufacturing defect may cause an increased risk of leakage and presents a risk of incidental exposure to biological hazards associated with direct contact
2023-10-19Meridian Bioscience IncDue to a manufacturing defect, certain Para-Pak vials may be at risk for leakage.
2023-05-15MEDLINE INDUSTRIES, LP - NorthfieldPotential for the labeled sterile ultrasound gel component within packs to not meet sterility specifications.

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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.