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In.pact admiral paclitaxelcoated pta balloon catheter

Official notice

4 Apr 2022

Last checked

4 Apr 2022

Medium riskHealth Canada

An official Health Canada notice concerns In.pact admiral paclitaxelcoated pta balloon catheter. During a routine inspection Medtronic noted there was damage to the sterile pouch that contains the In.Pact Admiral Catheters. Upon investigation, there had been a change implemented to one manufacturing line which may cause pouch damage. All batches manufactured on this line after that change are being retrieved. Damage to the pouch can cause a loss of sterility and may result in potential clinical harm of systemic reaction including infection. The affected units are limited to specific lot numbers of In.Pact Admiral Catheters. No other Medtronic products are affected by this issue. Through 11-March-2022, Medtronic has received no (0) complaints involving this issue. There are no actions required for patients where the affected In.Pact Admiral Catheters were used during a procedure. These patients should continue to be monitored in accordance with the medical facility's standard care protocols. Recall start date: Mar 25, 2022 Published 2022-04-04.

What to do now

Contact the manufacturer if you require additional information.

Recall number

64045

Official notice

2022-04-04

The hazard

During a routine inspection Medtronic noted there was damage to the sterile pouch that contains the In.Pact Admiral Catheters. Upon investigation, there had been a change implemented to one manufacturing line which may cause pouch damage. All batches manufactured on this line after that change are being retrieved. Damage to the pouch can cause a loss of sterility and may result in potential clinical harm of systemic reaction including infection. The affected units are limited to specific lot numbers of In.Pact Admiral Catheters. No other Medtronic products are affected by this issue. Through 11-March-2022, Medtronic has received no (0) complaints involving this issue. There are no actions required for patients where the affected In.Pact Admiral Catheters were used during a procedure. These patients should continue to be monitored in accordance with the medical facility's standard care protocols. Recall start date: Mar 25, 2022

How to check if you're affected

Compare the product name and identifiers below with the item you own. Follow the official notice if they match.

Lots

es

Recall Numbers

64045

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Affected products

Product 1

Affected Products - In.Pact Admiral Paclitaxelcoated Pta Balloon Catheter, Lot or Serial Number - Not applicable., Model or catalog number - ADM07006013P, ADM05004013P, ADM06008013P, ADM04015013P, ADM06004013P, ADM05008013P, ADM06015013P

Risk / hazard

During a routine inspection Medtronic noted there was damage to the sterile pouch that contains the In.Pact Admiral Catheters. Upon investigation, there had been a change implemented to one manufacturing line which may cause pouch damage. All batches manufactured on this line after that change are being retrieved. Damage to the pouch can cause a loss of sterility and may result in potential clinical harm of systemic reaction including infection. The affected units are limited to specific lot numbers of In.Pact Admiral Catheters. No other Medtronic products are affected by this issue. Through 11-March-2022, Medtronic has received no (0) complaints involving this issue. There are no actions required for patients where the affected In.Pact Admiral Catheters were used during a procedure. These patients should continue to be monitored in accordance with the medical facility's standard care protocols. Recall start date: Mar 25, 2022

Where it was sold

The source does not list specific retailers. See the official notice for where affected products were sold.

Location 1

CA · Canada

Affected area 1

CA · Canada

Company & contacts

Manufacturer

Not provided

Phone

Not provided

Brand: Medtronic, In.pact Admiral Paclitaxelcoated Pta Balloon Catheter.

Source & status

Source

Health Canada

Tier

official

Category

HEALTH

Classification

Type II

App estimate

medium

Recall details

Recall number

64045

Classification

Type II

Source tier

official

Documents, notices & source

See the official notice and source documents for full details.

View full official notice
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