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Adverse Event Report

3M 3M SCOTCH CAST   back to search results
Catalog Number 76005
Event Description

1. Too thin - not enough padding. 2. Not enough padding. 3. Peeled box correctly - 3" to 4" (heed) - wasted. 4. Insufficient padding for pt safety. A. Doesn't like padding only one side. B. Material is inferior. C. Sizing is incomplete.

 
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Brand Name3M SCOTCH CAST
Type of DeviceCAST
Baseline Device 510(K) Number
Baseline Device PMA Number
Manufacturer (Section D)
3M
*
Device Event Key340505
MDR Report Key351224
Event Key330854
Report NumberMW4003083
Device Sequence Number1
Product CodeITG
Report Source Voluntary
1 Device Was Involved in the Event
1 Patient Was Involved in the Event
Date FDA Received08/30/2001
Is This An Adverse Event Report? No
Device Operator Invalid Data
Device Catalogue Number76005
Was Device Available For Evaluation? No Answer Provided
Is the Device an Implant? No
Is this an Explanted Device?

Database last updated on January 30, 2009

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