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SPO2 Module (Mindray/Package/ accessory)

Shenzhen Mindray Bio-Medical Electronics Co., Ltd. · Model 115-047245-00 · UDI-DI 06944904096841

DQE Prescription
1
510(k) clearances
1,088
Adverse events (24 deaths)
14
Recalls
21
Facilities

Recalls

DateFirmReason
2021-07-09Edwards Lifesciences, LLCThere is a potential for internal leaks within catheters.
2021-07-09Edwards Lifesciences, LLCThere is a potential for internal leaks within catheters.
2021-07-09Edwards Lifesciences, LLCThere is a potential for internal leaks within catheters.
2021-07-09Edwards Lifesciences, LLCThere is a potential for internal leaks within catheters.
2021-07-09Edwards Lifesciences, LLCThere is a potential for internal leaks within catheters.
2021-07-09Edwards Lifesciences, LLCThere is a potential for internal leaks within catheters.
2020-03-27Edwards Lifesciences, LLCSterile catheter kit packaging compromised.
2020-01-02ICU Medical, Inc.Inability for the guidewire to pass through the needles included with the catheter kits.
2020-01-02ICU Medical, Inc.Inability for the guidewire to pass through the needles included with the catheter kits.
2020-01-02ICU Medical, Inc.Inability for the guidewire to pass through the needles included with the catheter kits.

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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.