[Recalled] Presource PBDS, Gyn Laparoscopy Kit, Circulator — Various Presource Kits contain a pre-assembled Filter and Anesthesia Circuit th… | FDA 2013-03-26

Authorities recorded a safety problem with this product. The details below come directly from the government recall notice.

Recall details

Why it was recalled

According to the FDA_DEVICE notice, the identified hazard is: Various Presource Kits contain a pre-assembled Filter and Anesthesia Circuit that may contain outer plastic packaging on one or more components. If the packaging is removed without disassembling the components, remnants of the plastic from the packaging material may become lodged in the filter potentially causing an obstruction of airflow.

This Class I recall concerns device products distributed in United States and was recorded by FDA_DEVICE. Recalls in this category are published so that owners, retailers, and importers can identify affected units and act quickly.

What to do if you own this product

Stop using the product immediately and follow the authority's remedy (return, repair, or disposal).

Read the full official notice →

Related recalls from Cardinal Health, Medical Products & Services

• Presource PBDS, Shoulder Procedure, Kit, Circulator — Class I
• Presource PBDS, Shoulder Arthroscopy, Kit, Circulator — Class I
• Presource PBDS, Knee Arthroscopy, Kit, Circulator — Class I
• Presource PBDS, Hand, Kit, Circulator — Class I
• A) Presource PBDS, Lap Chole, Kit, Clean Up; B) Presource PBDS, Greenwood LeFlore Hosp, Lap Chole, Kit — Class I
• Presource PBDS, Total Hip, Kit, Circulator — Class I

This page indexes a public government recall notice for reference. We do not sell or verify this product; always confirm the current status on the authority's official site.