Recall StatusOpen, Classified
Date Initiated2024-10-15
Product Quantity21 devices
Reason for Recall
The Bipolar assembly contains an oversized Retainer Ring.
Firm Action
The recalling firm issued letters on and dated 15-Oct-2024 via email informing the consignee of the issue, patient impact, risks to health, and actions to be taken by the user. The actions include:
1. Ensure that the contents of this Field Safety Notice are read and understood by those within your organization who may use the Tandem Bipolar 46OD 28ID.
2. Locate and quarantine affected devices immediately. If you have further distributed the product to other organizations, please inform them at once of this Field Action and provide them with a copy of this letter.
3. Please complete the Customer Response form and email or fax it to your national Smith+Nephew agency/distributor.
4. Return quarantined product to your national Smith+Nephew agency/distributor.
5. Please maintain awareness of this notice and resulting action for an appropriate period to ensure the effectiveness of the corrective action.
A Customer Response Form was enclosed for completion and return and a Physician Communication was enclosed to inform physicians of much of the same information as was contained in the Field Safety Notice regarding the issue and risks to health.
Root Cause
Under Investigation by firm
Distribution Pattern
International distribution to the countries of Australia, Belgium, Canada, Germany, Italy, Panama, Poland, Spain, and Turkey.
Related FDA 510(k) Records
Devices referenced by this recall via K-numbers.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.