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Simpurity

SAFE N' SIMPLE LLC · Model SNS58825 · UDI-DI 00810040134708

NAE
10
510(k) clearances
105
Adverse events
6
Recalls
304
Facilities

Description

Simpurity Hydrogel Wound Filler in a 25g Tube

Recalls

DateFirmReason
2020-02-11Nelson Innovaions, LlcForeign material near or along the edge of the hydrogel adhesive within the pouch packaging
2018-08-22Safe N Simple, LLCThe sterilization process used was unqualified.
2018-08-22Safe N Simple, LLCThe sterilization process used was unqualified.
2016-09-01CellEra LLCAdhesive border was not sticky enough.
2015-09-30O-Two Medical Technologies, Inc.For lack of evidence to validate effectiveness of sterilization dose, O-Two Medical Technologies Inc. hereby announces a voluntary medical device recall of the suspected batches o
2006-11-09Embeem Inc.Foreign material- this device, a sterile wound care product, was found to be contaminated with clumps of brown/black foreign material

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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.