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Arjo Wiggins Medical, Inc.

STERIMED INC. · Model 1010882020 · UDI-DI 00815588024207

FRG
1
510(k) clearances
222
Adverse events
50
Recalls
194
Facilities

Description

88 20X20,500_CASE VB

Recalls

DateFirmReason
2022-12-05Turbett Surgical, Inc.Pod may have weld failures breaching the sterile barrier and result in the use of unsterile instruments leading to infection or other major injuries.
2022-12-05Turbett Surgical, Inc.Pod may have weld failures breaching the sterile barrier and result in the use of unsterile instruments leading to infection or other major injuries.
2022-04-14Turbett Surgical, Inc.Devices were subject to unapproved rework processes.
2022-04-01TURBETT SURGICAL, LLCEight units manufactured before June 2019 have exhibited weld failures breaching the sterile barrier after prolonged use.
2020-12-02Steris CorporationPurple ink located on the outside label of Vis-U-All Pouches may migrate ( bleed ) following steam processing causing cosmetic defects on the exterior of the pouch and in some inst
2020-12-02Steris CorporationPurple ink located on the outside label of Vis-U-All Pouches may migrate ( bleed ) following steam processing causing cosmetic defects on the exterior of the pouch and in some inst
2020-12-02Steris CorporationPurple ink located on the outside label of Vis-U-All Pouches may migrate ( bleed ) following steam processing causing cosmetic defects on the exterior of the pouch and in some inst
2020-12-02Steris CorporationPurple ink located on the outside label of Vis-U-All Pouches may migrate ( bleed ) following steam processing causing cosmetic defects on the exterior of the pouch and in some inst
2020-12-02Steris CorporationPurple ink located on the outside label of Vis-U-All Pouches may migrate ( bleed ) following steam processing causing cosmetic defects on the exterior of the pouch and in some inst
2020-12-02Steris CorporationPurple ink located on the outside label of Vis-U-All Pouches may migrate ( bleed ) following steam processing causing cosmetic defects on the exterior of the pouch and in some inst

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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.