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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 5 of 5 Results
510(K) Number: K093623
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Product Description
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Recall
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FDA Recall
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Instrumentation Laboratory GEM Premier 4000 PN 00025000000 The GEM Premier 4000 is a portable cri... 2 05/10/2011 FEI # 1217183
Instrumentation Laboratory Co.
GEM PREMIER 4000 CARTRIDGE K+ REPORTING: GEM 4000 BG/Hct/Lytes/G/L/CO-Ox/tBili : 75 test iQM P... 1 07/21/2011 FEI # 1217183
Instrumentation Laboratory Co.
GEM PREMIER 4000 CARTRIDGE K+ REPORTING: GEM 4000 BG/Hct/Lytes/CO-Ox/tBili 75 test iQM Part N... 1 07/21/2011 FEI # 1217183
Instrumentation Laboratory Co.
GEM PREMIER 4000 CARTRIDGE K+ REPORTING: GEM 4000 BG/Hct/Lytes/CO-Ox 75 test iQM Part Number... 1 07/21/2011 FEI # 1217183
Instrumentation Laboratory Co.
GEM PREMIER 4000 CARTRIDGE K+ REPORTING: GEM 4000 BG/Hct/Lytes/G/L/CO-Ox 75 test iQM Part Numbe... 1 07/21/2011 FEI # 1217183
Instrumentation Laboratory Co.
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