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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: COVIDIEN 1/2ML INSULIN SYR 28G X 1/2 RP; SYRINGE, PISTON

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COVIDIEN 1/2ML INSULIN SYR 28G X 1/2 RP; SYRINGE, PISTON Back to Search Results
Model Number 8881500014
Device Problem Detachment of Device or Device Component (2907)
Patient Problem No Consequences Or Impact To Patient (2199)
Event Date 02/10/2020
Event Type  malfunction  
Manufacturer Narrative
Additional information and the incident sample has been requested but to date has not been received for evaluation.If the sample is received, or if additional information pertinent to the incident is obtained a follow-up report will be submitted.As part of our manufacturing process, all device history records are reviewed and approved by quality, prior to release of product.
 
Event Description
The customer reported, the needle kept falling off.
 
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Brand Name
1/2ML INSULIN SYR 28G X 1/2 RP
Type of Device
SYRINGE, PISTON
Manufacturer (Section D)
COVIDIEN
1222 sherwood rd
norfolk NE 68701
Manufacturer (Section G)
COVIDIEN
1222 sherwood rd
norfolk NE 68701
Manufacturer Contact
jill saraiva
15 hampshire street
mansfield, MA 02048
5086183640
MDR Report Key9746261
MDR Text Key181995847
Report Number1915484-2020-01137
Device Sequence Number1
Product Code FMF
UDI-Device Identifier10884521014893
UDI-Public10884521014893
Combination Product (y/n)N
Reporter Country CodeUS
Number of Events Reported1
Summary Report (Y/N)N
Report Source Manufacturer
Source Type company representative,distri
Reporter Occupation Other
Type of Report Initial
Report Date 02/24/2020
1 Device was Involved in the Event
1 Patient was Involved in the Event
Date FDA Received02/24/2020
Is this an Adverse Event Report? No
Is this a Product Problem Report? Yes
Device Operator No Information
Device Model Number8881500014
Device Catalogue Number8881500014
Device Lot Number913351X
Was Device Available for Evaluation? Yes
Date Manufacturer Received02/11/2020
Is the Device Single Use? Yes
Type of Device Usage N
Patient Sequence Number1
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