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Model Number UNK-BIOPSYFORCEPS |
Device Problem
Adverse Event Without Identified Device or Use Problem (2993)
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Patient Problem
Thrombosis/Thrombus (4440)
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Event Date 01/01/1980 |
Event Type
Injury
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Manufacturer Narrative
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Additional information is pending and will be submitted within 30 days upon receipt.Without a lot number to conduct a device history record (dhr) review, it is not possible to determine if the reported failure could be related to the manufacturing process.
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Event Description
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As reported, biopsy forceps active post-market surveillance survey indicated they had experienced permanent atrial ventricular block, hemorrhages, pericardial effusion, and thrombosis.The device will not be returned for evaluation.
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Manufacturer Narrative
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Biopsy forceps active post-market surveillance survey indicated they had experienced permanent atrial ventricular block, hemorrhages, pericardial effusion, and thrombosis.The product was not returned for analysis.No lot number was provided therefore a product history record (phr) review could not be generated.Without the return of the device for analysis and based on the information provided, the reported ¿embolism¿ was not confirmed.Procedural and or handling factors such the user¿s interaction with the device may have led to the reported event.Additionally, no procedural images or films have been made available.According to the instructions for use ¿procedures requiring biopsy forceps should not be attempted by physicians unfamiliar with the possible complications.Complications may occur at any time during or after the procedure.Possible complications include but are not limited to hematoma at the puncture site, infection, perforation of the vessel wall or the myocardium vessel trauma, embolism and death.¿ additionally, refer to the ¿description¿ section for aid in selecting the size of the sheath introducer and biopsy forceps to be used.Using fluoroscopy, advance the forceps through the appropriate sheath introducer and into the right or left ventricle.Note: when using the 104 cm biopsy forceps, confirm the position of the sheath introducer in the ventricle prior to each biopsy to be performed.After confirming that the tip of the forceps is in the ventricle, open the jaws.Advance the open jaws to the heart wall.Close the jaws firmly to obtain a tissue specimen.Maintain sufficient pressure on the double rings to assure retention of specimen during withdrawal.Note: closing of the jaws and withdrawal of the bioptome should be performed in a single motion.Flush the sheath introducer continuously with heparinized saline while slowly withdrawing the forceps.Remove the sample from jaws.Rinse bioptome before and after each biopsy.Repeat steps 2 thru 7 until sufficient tissue volume is obtained.¿neither the phr review nor the information available suggests a design or manufacturing related cause could be related to the manufacturing process of the unit.Therefore, no corrective or preventive actions will be taken.
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Event Description
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As reported, biopsy forceps active post-market surveillance survey indicated they had experienced permanent atrial ventricular block, hemorrhages, pericardial effusion, and thrombosis.The device will not be returned for evaluation.
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Search Alerts/Recalls
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