C.R. BARD, INC. (BASD) -3006260740 MINILOC SAFETY INFUSION SET 20G X 1IN; SET, ADMINISTRATION, INTRAVASCULAR
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Model Number N/A |
Device Problem
Unsealed Device Packaging (1444)
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Patient Problem
No Clinical Signs, Symptoms or Conditions (4582)
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Event Date 03/30/2022 |
Event Type
malfunction
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Manufacturer Narrative
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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.
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Event Description
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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.
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Manufacturer Narrative
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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.
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Event Description
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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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