Smiths Medical ASD, Inc Anesthesia and Safety Devices Division Portex Inner Cannula for Tracheostomy Tube Size 7.0 mm, REF Code 566070 Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Portex Inner Cannula for Tracheostomy Tube Size 7.0 mm, REF Code 566070
Brand
Smiths Medical ASD, Inc Anesthesia and Safety Devices Division
Lot Codes / Batch Numbers
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Products Sold
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Smiths Medical ASD, Inc Anesthesia and Safety Devices Division is recalling Portex Inner Cannula for Tracheostomy Tube Size 7.0 mm, REF Code 566070 due to Incompatible products may cause potential trachea trauma. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Incompatible products may cause potential trachea trauma
Recommended Action
Per FDA guidance
Smiths Medical ASD notified the consignees by letter, dated 5/21/04. All responses to the notification are to be completed by fax and directed to Smiths Medical Regulatory Affairs Departement. The recalled products are to be returned and scrapped by Smiths Medical.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026