Monitor U.S. medical device recall enforcement reports from the FDA. Review product descriptions, recall reasons, classifications, dates, recalling firms and distribution information where the FDA provides them.
26,155 detailed records are currently available in this category.
Potential for fluid leakage out of air vents on inline filters on Plum and Sapphire micropore infusion sets.
Potential for fluid leakage out of air vents on inline filters on Plum and Sapphire micropore infusion sets.
Berkeley Disposa-Filter may possess an insufficient ultrasonic weld defect which joins the two-halves of the filter cartridge, thus the housing could separate
There is a potential for a progressive decline in observed ICP readings of the monitor during use.
Potential for fluid leakage out of air vents on inline filters on Plum and Sapphire micropore infusion sets.
Potential for fluid leakage out of air vents on inline filters on Plum and Sapphire micropore infusion sets.
Potential for fluid leakage out of air vents on inline filters on Plum and Sapphire micropore infusion sets.
Due to low Quality Control recovery and invalid Calibration.
Potential for fluid leakage out of air vents on inline filters on Plum and Sapphire micropore infusion sets.
Potential for fluid leakage out of air vents on inline filters on Plum and Sapphire micropore infusion sets.
Potential for fluid leakage out of air vents on inline filters on Plum and Sapphire micropore infusion sets.
Potential for fluid leakage out of air vents on inline filters on Plum and Sapphire micropore infusion sets.
Potential for fluid leakage out of air vents on inline filters on Plum and Sapphire micropore infusion sets.
The action was initiated due power supply failure. During a power supply failure the instruments malfunctions and no patient results are produced.
Interference can occur between the adolescent attachment bolt and the adolescent nail, cause a delay in surgical procedures
Medtronic has determined that some catheters have a slightly higher diameter stylette causing removal difficulties.
The action was initiated due power supply failure. During a power supply failure the instruments malfunctions and no patient results are produced.
Potential for fluid leakage out of air vents on inline filters on Plum and Sapphire micropore infusion sets.
The action was initiated due power supply failure. During a power supply failure the instruments malfunctions and no patient results are produced.
Due to low Quality Control recovery and invalid Calibration.
Potential for fluid leakage out of air vents on inline filters on Plum and Sapphire micropore infusion sets.
Potential for fluid leakage out of air vents on inline filters on Plum and Sapphire micropore infusion sets.
The action was initiated due power supply failure. During a power supply failure the instruments malfunctions and no patient results are produced.
Atellica CH 930 Analyzer - Erroneous Indices for Hemolysis and Lipemia in Software versions 1.19.2 and below
Medical device recall records can change as the FDA receives additional information. Check the official record identifier and current FDA information before making health or product-use decisions.
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This database is designed for discovery and reference. It can help you locate a relevant recall record, identify the recalling firm or NHTSA campaign, compare dates and classifications, and follow the official source. It is not a substitute for a VIN-specific NHTSA check, a manufacturer notice, medical advice or instructions issued by the recalling company.
