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U.S. Department of Health and Human Services

MAUDE - Manufacturer and User Facility Device Experience

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Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
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18 records meeting your search criteria returned- Product Code: LRO Product Problem: Contamination of Device Ingredient or Reagent Report Date From: 01/1/2016
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ManufacturerBrand NameDate Report Received
DEROYAL INDUSTRIES, INC. DEROYAL 11/03/2020
AMERICAN CONTRACT SYSTEMS, INC. ACS 09/18/2019
AMERICAN CONTRACT SYSTEMS CUSTOM MINOR PACK 09/12/2019
AMERICAN CONTRACT SYSTEMS, INC. ACS 08/23/2019
AMERICAN CONTRACT SYSTEMS, INC. ACS 08/07/2019
AMERICAN CONTRACT SYSTEMS, INC. ACS 08/01/2019
MEDLINE INDUSTRIES, INC. MEDLINE MAJOR GENERAL PACK 07/12/2019
MEDLINE INDUSTRIES "VASCULAR" PACK 01/07/2019
CARDINAL HEALTH 200, LLC CARDINAL CUSTOM PACK 06/27/2018
MEDLINE INDUSTRIES TOTAL KNEE PACK - LF 03/14/2018
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