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U.S. Department of Health and Human Services

Medical Device Recalls
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Related Medical Device Recalls
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Product Description
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FDA Recall
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Z-0478-2022 - OCT-Camera 211 01 A3; Running software iOCT-Control 3 v1.4 2 01/10/2022 Haag-Streit USA Inc
Z-0477-2022 - OCT-Camera 211 01 A1, Running software iOCT-Control 3 v1.4 2 01/10/2022 Haag-Streit USA Inc
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