MAUDE Adverse Event Report: CLEARSTREAM TECHNOLOGIES LTD. LIFESTREAM; BALLOON EXPANDABLE VASCULAR COVERED STENT

Catalog Number LSM1350537

Device Problem Device Dislodged or Dislocated (2923)

Patient Problem No Clinical Signs, Symptoms or Conditions (4582)

Event Date 09/07/2020

Event Type  malfunction  

Manufacturer Narrative

A device history record review was conducted and there was nothing found to indicate there was a manufacturing related cause for this event.Per the complaint history review, this is the first complaint reported for this product/lot number combination.The sample was returned for evaluation.The stent was returned on the balloon and dislocated by 0.5mm toward the proximal bond.It was easily removed during the evaluation and had not been expanded.The result of the investigation is confirmed for stent dislodgement.The root cause for the dislodgement issue could not be determined based upon the available information received from the field communications and device evaluation.A review of product labeling documents (e.G.Procedural instructions, indications, warnings, precautions, cautions, possible complications, contraindications, and unit label) showed that the product labeling is adequate.The catalog number identified in section has not been cleared in the us but is similar to the lifestream products that are cleared in the us.The pro code and 510k number for the lifestream products are identified.(expiry date: 10/2021).

Event Description

It was reported that as the radiologist was advancing the lifestream device into the 6fr introducer sheath the stent dislodged at the hemostasis valve.The stent was retrieved and the procedure was successfully completed using an atrium device.There was no reported patient injury.

Event Description

It was reported that as the radiologist was advancing the lifestream device into the 6fr introducer sheath the stent dislodged at the hemostasis valve.The stent was retrieved and the procedure was successfully completed using an atrium device.There was no reported patient injury.

Manufacturer Narrative

H10: the initial mdr capturing this event was reported with an incorrect g4 date.The correct g4 date should have been (b)(6)2020.The catalog number identified in section d4 has not been cleared in the us but is similar to the lifestream products that are cleared in the us.The pro code and 510 k number for the lifestream products are identified in d2 and g5.H10: manufacturing review: a device history record review was conducted and there was nothing found to indicate there was a manufacturing related cause for this event.Per the complaint history review, this is the first complaint reported for this product/lot number combination.Investigation summary: the sample was returned for evaluation.The stent was returned on the balloon and dislocated by 0.5mm toward the proximal bond.It was easily removed during the evaluation and had not been expanded.The result of the investigation is confirmed for stent dislodgement.The root cause for the dislodgement issue could not be determined based upon the available information received from the field communications and device evaluation.Labeling review: a review of product labeling documents (e.G.Procedural instructions, indications, warnings, precautions, cautions, possible complications, contraindications, and unit label) showed that the product labeling is adequate.H10: d4 (expiry date: 10/2021).H3 other text : see h10.

Event Description

It was reported that as the radiologist was advancing the lifestream device into the 6fr introducer sheath the stent dislodged at the hemostasis valve.The stent was retrieved and the procedure was successfully completed using an atrium device.There was no reported patient injury.

Manufacturer Narrative

The catalog number identified in section d4 has not been cleared in the us but is similar to the lifestream products that are cleared in the us.The pro code and 510 k number for the lifestream products are identified in d2 and g4.Manufacturing review: a device history record review was conducted and there was nothing found to indicate there was a manufacturing related cause for this event.Per the complaint history review, this is the first complaint reported for this product/lot number combination.Investigation summary: the sample was returned for evaluation.The stent was returned on the balloon and dislocated by 0.5mm toward the proximal bond.It was easily removed during the evaluation and had not been expanded.The result of the investigation is confirmed for stent dislodgement.The root cause for the dislodgement issue could not be determined based upon the available information received from the field communications and device evaluation.Labeling review: the instruction for use for the lifestream product was reviewed and contains the following information relevant to the reported event: precautions: the device should only be used by physicians who are trained in endovascular procedures and are familiar with the complications, side effects and hazards of peripheral vascular interventions.Prior to device use, refer to the covered stent sizing table on the label and read the instructions for use.Crossing the implant with catheters or other adjunct devices can result in covered stent dislodgement or damage.Potential patient/device adverse effects that may occur include, but are not limited to, the following: covered stent dislodgement from balloon during tracking procedure; covered stent misplacement during placement procedure.Directions for use: site access and preparation: using standard techniques access the artery and place an introducer sheath or guiding catheter of appropriate inner diameter and a 0.035" (0.89 mm) guidewire across the target lesion.Covered stent size selection: select a covered stent diameter that is approximately 5%-20% larger than the largest reference vessel diameter at the proximal or distal target site.Refer to the sizing table on the packaging label for appropriate selection of the covered stent diameter and length.Endovascular system preparation: carefully remove the selected device from the package.Inspect the covered stent for adherence to the balloon and centered placement in relation to the balloon marker bands.If the covered stent is not centered and/or does not firmly adhere to the balloon, do not use.Flush the delivery system guidewire lumen with sterile saline mixture until saline drops from the distal end of the endovascular system.Air evacuation: a 20 cc or smaller luer-lock syringe with a minimum of 5 cc¿s sterile saline mixture is recommended for use for aspirating this device.With the distal balloon tip pointing down and positioned below the level of the syringe, pull negative pressure until all air is expelled.Induce a negative pressure to remove any air from the balloon and inflation lumen.Repeat until all air is expelled.10.Carefully release to neutral.Allow the inflation lumen to fill with the diluted contrast medium and maintain a neutral pressure.Important: do not apply positive pressure to the balloon.Attach the prefilled inflation device to the inflation lumen of the catheter hub, ensuring no air bubbles remain at the catheter connection.Verify that the covered stent is still centered between the two radiopaque markers on the balloon catheter.Introduction of the endovascular system and placement of the covered stent: advance the endovascular system over the guidewire into the introducer sheath.D4 (expiry date: 10/2021).H11: section a through f ¿ the information provide by bd represents all 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.

• Brand Name: LIFESTREAM
• Type of Device: BALLOON EXPANDABLE VASCULAR COVERED STENT
• Manufacturer (Section D): CLEARSTREAM TECHNOLOGIES LTD.; moyne upper; enniscorthy, co. wexford N A ; EI N A
• MDR Report Key: 11062673
• MDR Text Key: 225339098
• Report Number: 9616666-2020-20036
• Device Sequence Number: 1
• Product Code: PRL
• Combination Product (y/n): N
• PMA/PMN Number: P160024
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Manufacturer
• Source Type: company representative,foreig
• Type of Report: Initial,Followup,Followup
• Report Date: 09/20/2021

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Date FDA Received: 12/23/2020
• Is this an Adverse Event Report?: No
• Is this a Product Problem Report?: Yes
• Device Operator: Health Professional
• Device Catalogue Number: LSM1350537
• Device Lot Number: CMCY0426
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Date Returned to Manufacturer: 10/19/2020
• Date Manufacturer Received: 09/08/2021
• Is This a Reprocessed and Reused Single-Use Device?: No
• Patient Sequence Number: 1
• Patient Outcome(s): Other