Medical Device Recalls

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Related Medical Device Recalls

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Product Description	Recall Class	FDA Recall Posting Date	Recalling Firm
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Z-2850-2011 - "*REF: 24-3050 TMJ SYSTEM OnPoint SCOPE PROCEDURE KITSTERILE PRODUCTSTERILE EO*KIT CONTAINS BOTH STERILE AND NON-STERILE COMPONENTS Distributed by: BIOMET MICROFIXATION 1520 TRADEPORT DRI...	2	07/19/2011	FEI # 1032347 Biomet Microfixation, Inc.
Z-2852-2011 - "*REF: 24-4050 TMJ SYSTEM ArthroSimplicity KITSTERILE PRODUCTSTERILE EO*KIT CONTAINS BOTH STERILE AND NON-STERILE COMPONENTS DISTRIBUTED BY: BIOMET MICROFIXATION 1520 TRADEPORT DRIVE JACKS...	2	07/19/2011	FEI # 1032347 Biomet Microfixation, Inc.
Z-2849-2011 - "*REF: 922070 TMJ SYSTEM ARTHROSIMPLICITY KITSTERILE PRODUCTSTERILE EODISTRIBUTED BY BIOMET MICROFIXATION 1520 TRADEPORT DRIVE JACKSONVILLE, FL 32218 USA www.biometmicrofixation.com**" ...	2	07/19/2011	FEI # 1032347 Biomet Microfixation, Inc.
Z-2851-2011 - "*REF: 922090 TMJ SYSTEM InnerVue SCOPE PROCEDURE KITSTERILE PRODUCTSTERILE EO*KIT CONTAINS BOTH STERILE AND NON-STERILE COMPONENTS DISTRIBUTED BY: BIOMET MICROFIXATION 1520 TRADEPORT DRI...	2	07/19/2011	FEI # 1032347 Biomet Microfixation, Inc.