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U.S. Department of Health and Human Services

Manufacturer and User Facility Device Experience (MAUDE)

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510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
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93 records meeting your search criteria returned- Product Code: FMI Product Problem: Device Contaminated During Manufacture or Shipping Report Date From: 01/1/2009

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ManufacturerBrand NameDate Report Received
BD BD PEN NED UF SHORT 8MM 90S - 31G 5/16 12/27/2021
CARDINAL HEALTH SAFETY NEEDLE 23 X 1 06/25/2021
BECTON, DICKINSON AND COMPANY (BD) BD VACUTAINER PRECISIONGLIDE MULTIPLE SA 05/24/2021
COVIDIEN LIFSHLD 250-E 18X1 RBLT 04/23/2021
COVIDIEN SAFETY NEEDLE 25 G X 1" 10/22/2020
COVIDIEN SAFETY NEEDLE 25 G X 1" 12/16/2019
COVIDIEN SAFETY NEEDLE 25 G X 1" 11/19/2019
COVIDIEN "SAFETY NEEDLE 23GX1 BULK, NS" 06/28/2019
COVIDIEN SAFETY NEEDLE 23 X 1 05/14/2019
COVIDIEN SAFETY NEEDLE 25 X 1 02/21/2019
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