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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 9 of 9 Results
Related Medical Device Recalls
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Product Description
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Z-0010-2025 - CADD Medication Cassette Reservoir, 100mL, Product Code 21-7002-24 2 10/18/2024 FEI # 3012307300
Smiths Medical ASD Inc.
Z-0011-2025 - CADD Medication Cassette Reservoir, 100mL, FS, Product Code 21-7302-24 2 10/18/2024 FEI # 3012307300
Smiths Medical ASD Inc.
Z-0012-2025 - CADD Medication Cassette Reservoir, 100mL, FS, YELLOW, Product Code 21-7300-24 2 10/18/2024 FEI # 3012307300
Smiths Medical ASD Inc.
Z-0013-2025 - CADD Medication Cassette Reservoir, 50mL, FS, Product Code 21-7301-24 2 10/18/2024 FEI # 3012307300
Smiths Medical ASD Inc.
Z-0018-2025 - ENT RES, 100 ML, Non-Sterile W CLAMP & FEMALE LUER, Product Code 68-2231-28 2 10/18/2024 FEI # 3012307300
Smiths Medical ASD Inc.
Z-0015-2025 - CADD Medication Cassette Reservoir, 100mL, FS, Product Code 21-7302-24JP 2 10/18/2024 FEI # 3012307300
Smiths Medical ASD Inc.
Z-0016-2025 - CADD Medication Cassette Reservoir, 50mL, FS, Product Code 21-7301-24JP 2 10/18/2024 FEI # 3012307300
Smiths Medical ASD Inc.
Z-0017-2025 - ENT RES 100 ML Non-Sterile W CLAMP, TUBING FLAG, & FEMALE LUER, Product Code 68-2230-28 2 10/18/2024 FEI # 3012307300
Smiths Medical ASD Inc.
Z-0014-2025 - CADD Medication Cassette Reservoir, 50mL, Product Code 21-7001-24 2 10/18/2024 FEI # 3012307300
Smiths Medical ASD Inc.
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