FDA Device Intelligence
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Container, Specimen, Non-Sterile

FDA product code NNI · Class 1 · Pathology

1,694
Registered devices
28
Adverse events
4
Recalls
0
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2026-03-09Milestone S.R.L.There is a possibility of reagent leakage from the specimen container.
2021-12-01MEDLINE INDUSTRIES, LP - NorthfieldProduct stored incorrectly in temperature controlled setting instead of refrigeration.
2016-03-03Dynarex CorporationExterior carton is mis-labeled as Sterile. Non-sterile, bulk specimen containers were packed in incorrect exterior carton.
2011-02-18Cardinal Health IncIn one lot of product (lot# 1091745), the label for the small version of the sock (catalog number 65652-123) was improperly used for the larger version of the p

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