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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: C.R. BARD, INC. (BASD) -3006260740 MINILOC SAFETY INFUSION SET 20G X 1IN; SET, ADMINISTRATION, INTRAVASCULAR

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C.R. BARD, INC. (BASD) -3006260740 MINILOC SAFETY INFUSION SET 20G X 1IN; SET, ADMINISTRATION, INTRAVASCULAR Back to Search Results
Model Number N/A
Device Problem Unsealed Device Packaging (1444)
Patient Problem No Clinical Signs, Symptoms or Conditions (4582)
Event Date 03/30/2022
Event Type  malfunction  
Manufacturer Narrative
The date of event was not provided by the complainant/reporter, the date reflected in this report is the date bd became aware of the event.The manufacturer has received the sample and will evaluate.Results are expected soon.A lot history review (lhr) of asens0010 showed no other similar product complaint(s) from this lot number.
 
Event Description
It was reported "package without seal, exposing the material to external environment." on 01.Apr.2022, distributor provides the following: was issue noticed prior, during or after use? was product used even though situation was observed prior it? r: prior use.
 
Manufacturer Narrative
H11: section a through f - the information provided by bd represents all of the known information at this time.Despite good faith efforts to obtain additional information, the complainant / reporter was unable or unwilling to provide any further patient, product, or procedural details to bd.The following were reviewed as part of this investigation: patient severity, complaint and lot history review, applicable previous investigation(s), sample (if available), and applicable fmea documents.Based on a review of this information, the following was concluded: the complaint of a missing seal is confirmed and was determined to be supplier related.One 20 g x 1.0 in.Miniloc safety infusion set was returned for evaluation.An initial visual observation showed one side of the pouch was not sealed and showed no evidence of sealing.No damage was observed on the product or the product packaging.The lack of evidence of a seal on one side of the returned package indicates the pouch was likely not sealed during the assembly process at the supplier.H3 other text : evaluation findings are in section h.11.
 
Event Description
It was reported "package without seal, exposing the material to external environment." on (b)(4)2022, distributor provides the following: - was issue noticed prior, during or after use? was product used even though situation was observed prior it? r: prior use.
 
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Brand Name
MINILOC SAFETY INFUSION SET 20G X 1IN
Type of Device
SET, ADMINISTRATION, INTRAVASCULAR
Manufacturer (Section D)
C.R. BARD, INC. (BASD) -3006260740
605 north 5600 west
salt lake city 84116
Manufacturer (Section G)
C.R. BARD, INC. (BASD) -3006260740
605 north 5600 west
salt lake city 84116
Manufacturer Contact
kelsey erickson
605 north 5600 west
salt lake city 84116
8015950700
MDR Report Key14170262
MDR Text Key289774475
Report Number3006260740-2022-01380
Device Sequence Number1
Product Code FPA
UDI-Device Identifier00801741048722
UDI-Public(01)00801741048722
Combination Product (y/n)N
Reporter Country CodeBR
PMA/PMN Number
K050600
Number of Events Reported1
Summary Report (Y/N)N
Report Source Manufacturer
Source Type Other,Distributor
Reporter Occupation Other Health Care Professional
Type of Report Initial,Followup
Report Date 06/21/2022
1 Device was Involved in the Event
1 Patient was Involved in the Event
Date FDA Received04/21/2022
Is this an Adverse Event Report? No
Is this a Product Problem Report? Yes
Device Operator Health Professional
Device Model NumberN/A
Device Catalogue NumberS02020-10
Device Lot NumberASENS0010
Was Device Available for Evaluation? Device Returned to Manufacturer
Date Returned to Manufacturer04/11/2022
Is the Reporter a Health Professional? Yes
Date Manufacturer Received06/21/2022
Was Device Evaluated by Manufacturer? Yes
Date Device Manufactured01/01/2020
Is the Device Single Use? Yes
Is This a Reprocessed and Reused Single-Use Device? No
Type of Device Usage Initial
Patient Sequence Number1
Patient Outcome(s) Other;
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