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IOB

Jiangmen Dacheng Medical Equipment Co., Ltd. · Model Medium · UDI-DI 06951013000409

HIB
1
510(k) clearances
152
Adverse events
6
Recalls
116
Facilities

Recalls

DateFirmReason
2026-07-13OBP Medical CorporationThere is a potential for vaginal speculums to contain a burr on the proximal plastic blade, which may introduce a sharp edge in the contact regions for both the patient and the hea
2025-06-11CooperSurgical, Inc.The HSG Procedure Trays and Endosee System Convenience Kits contain non-sterile iodine pouches, however the peel away lid labels incorrectly identify the iodine pouches as sterile.
2025-06-11CooperSurgical, Inc.The HSG Procedure Trays and Endosee System Convenience Kits contain non-sterile iodine pouches, however the peel away lid labels incorrectly identify the iodine pouches as sterile.
2025-06-11CooperSurgical, Inc.The HSG Procedure Trays and Endosee System Convenience Kits contain non-sterile iodine pouches, however the peel away lid labels incorrectly identify the iodine pouches as sterile.
2015-10-02Welch Allyn IncThe firm became aware that the KleenSpec 788 Corded Illuminator has the potential to be incorrectly connected to a commonly available AC power cord instead of the illuminator low v
2015-04-13CooperSurgical, Inc.Small sized specula were incorrectly packaged in printed bags for the medium sized speculum

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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.